Year |
Citation |
Score |
2024 |
Ai HJ, Kim ST, Liu C, Buchwald SL. Correction to "Copper-Catalyzed Amination of Aryl Chlorides under Mild Reaction Conditions". Journal of the American Chemical Society. PMID 39411914 DOI: 10.1021/jacs.4c13491 |
0.379 |
|
2024 |
Feng K, Raguram ER, Howard JR, Peters E, Liu C, Sigman MS, Buchwald SL. Development of a Deactivation-Resistant Dialkylbiarylphosphine Ligand for Pd-Catalyzed Arylation of Secondary Amines. Journal of the American Chemical Society. 146: 26609-26615. PMID 39288263 DOI: 10.1021/jacs.4c09667 |
0.373 |
|
2024 |
Ai HJ, Kim ST, Liu C, Buchwald SL. Copper-Catalyzed Amination of Aryl Chlorides under Mild Reaction Conditions. Journal of the American Chemical Society. PMID 39283164 DOI: 10.1021/jacs.4c10237 |
0.423 |
|
2024 |
Strauss MJ, Liu KX, Greaves ME, Dahl JC, Kim ST, Wu YJ, Schmidt MA, Scola PM, Buchwald SL. Cu-Catalyzed Amination of Base-Sensitive Aryl Bromides and the Chemoselective N- and O-Arylation of Amino Alcohols. Journal of the American Chemical Society. PMID 38924516 DOI: 10.1021/jacs.4c05246 |
0.366 |
|
2024 |
Garhwal S, Dong Y, Mai BK, Liu P, Buchwald SL. CuH-Catalyzed Regio- and Enantioselective Formal Hydroformylation of Vinyl Arenes. Journal of the American Chemical Society. PMID 38723265 DOI: 10.1021/jacs.4c04287 |
0.377 |
|
2024 |
Strauss MJ, Greaves ME, Kim ST, Teijaro CN, Schmidt MA, Scola PM, Buchwald SL. Room-Temperature Copper-Catalyzed Etherification of Aryl Bromides. Angewandte Chemie (International Ed. in English). e202400333. PMID 38359082 DOI: 10.1002/anie.202400333 |
0.344 |
|
2023 |
Kutateladze DA, Mai BK, Dong Y, Zhang Y, Liu P, Buchwald SL. Stereoselective Synthesis of Trisubstituted Alkenes via Copper Hydride-Catalyzed Alkyne Hydroalkylation. Journal of the American Chemical Society. 145: 17557-17563. PMID 37540777 DOI: 10.1021/jacs.3c06479 |
0.439 |
|
2023 |
Kim ST, Strauss MJ, Cabré A, Buchwald SL. Room-Temperature Cu-Catalyzed Amination of Aryl Bromides Enabled by DFT-Guided Ligand Design. Journal of the American Chemical Society. PMID 36926889 DOI: 10.1021/jacs.3c00500 |
0.348 |
|
2023 |
Ye Y, Kim ST, King RP, Baik MH, Buchwald SL. Studying Regioisomer Formation in the Pd-Catalyzed Fluorination of Cyclic Vinyl Triflates: Evidence for in situ Ligand Modification. Angewandte Chemie (International Ed. in English). e202300109. PMID 36775802 DOI: 10.1002/anie.202300109 |
0.383 |
|
2023 |
Reichert EC, Feng K, Sather AC, Buchwald SL. Pd-Catalyzed Amination of Base-Sensitive Five-Membered Heteroaryl Halides with Aliphatic Amines. Journal of the American Chemical Society. 145: 3323-3329. PMID 36719903 DOI: 10.1021/jacs.2c13520 |
0.809 |
|
2022 |
Rojas AJ, Wolfe JM, Dhanjee HH, Buslov I, Truex NL, Liu RY, Massefski W, Pentelute BL, Buchwald SL. Palladium-peptide oxidative addition complexes for bioconjugation. Chemical Science. 13: 11891-11895. PMID 36320916 DOI: 10.1039/d2sc04074c |
0.61 |
|
2022 |
Knippel JL, Ni AZ, Schuppe AW, Buchwald SL. A General Strategy for the Asymmetric Preparation of α-Stereogenic Allyl Silanes, Germanes, and Boronate Esters via Dual Copper Hydride- and Palladium-Catalysis. Angewandte Chemie (International Ed. in English). PMID 36137941 DOI: 10.1002/anie.202212630 |
0.36 |
|
2022 |
Feng S, Dong Y, Buchwald SL. Enantioselective Hydrocarbamoylation of Alkenes. Angewandte Chemie (International Ed. in English). e202206692. PMID 35657208 DOI: 10.1002/anie.202206692 |
0.372 |
|
2022 |
Dong Y, Schuppe AW, Mai BK, Liu P, Buchwald SL. Confronting the Challenging Asymmetric Carbonyl 1,2-Addition Using Vinyl Heteroarene Pronucleophiles: Ligand-Controlled Regiodivergent Processes through a Dearomatized Allyl-Cu Species. Journal of the American Chemical Society. PMID 35341240 DOI: 10.1021/jacs.2c00734 |
0.358 |
|
2021 |
Hou CJ, Schuppe AW, Knippel JL, Ni AZ, Buchwald SL. A Dual CuH- and Pd-Catalyzed Stereoselective Synthesis of Highly Substituted 1,3-Dienes. Organic Letters. 23: 8816-8821. PMID 34726414 DOI: 10.1021/acs.orglett.1c03324 |
0.394 |
|
2021 |
King RP, Krska SW, Buchwald SL. A Neophyl Palladacycle as an Air- and Thermally Stable Precursor to Oxidative Addition Complexes. Organic Letters. PMID 34613744 DOI: 10.1021/acs.orglett.1c02307 |
0.658 |
|
2021 |
King RP, Krska SW, Buchwald SL. A Ligand Exchange Process for the Diversification of Palladium Oxidative Addition Complexes. Organic Letters. PMID 34319123 DOI: 10.1021/acs.orglett.1c02101 |
0.635 |
|
2021 |
Schuppe AW, Knippel JL, Borrajo-Calleja GM, Buchwald SL. Enantioselective Hydroalkenylation of Olefins with Enol Sulfonates Enabled by Dual Copper Hydride and Palladium Catalysis. Journal of the American Chemical Society. 143: 5330-5335. PMID 33784090 DOI: 10.1021/jacs.1c02117 |
0.419 |
|
2021 |
Feng S, Buchwald SL. CuH-Catalyzed Regio- and Enantioselective Hydrocarboxylation of Allenes: Toward Carboxylic Acids with Acyclic Quaternary Centers. Journal of the American Chemical Society. PMID 33761252 DOI: 10.1021/jacs.1c01880 |
0.318 |
|
2021 |
Jbara M, Rodriguez J, Dhanjee HH, Loas A, Buchwald SL, Pentelute BL. Oligonucleotide Bioconjugation with Bifunctional Palladium Reagents. Angewandte Chemie (International Ed. in English). PMID 33730425 DOI: 10.1002/anie.202103180 |
0.338 |
|
2021 |
Knippel JL, Ye Y, Buchwald SL. Enantioselective C2-Allylation of Benzimidazoles Using 1,3-Diene Pronucleophiles. Organic Letters. PMID 33646778 DOI: 10.1021/acs.orglett.1c00306 |
0.409 |
|
2020 |
Feng S, Hao H, Liu P, Buchwald SL. Diastereo- and Enantioselective CuH-Catalyzed Hydroamination of Strained Trisubstituted Alkenes. Acs Catalysis. 10: 282-291. PMID 33664986 DOI: 10.1021/acscatal.9b04871 |
0.362 |
|
2020 |
Dhanjee HH, Buslov I, Windsor IW, Raines RT, Pentelute BL, Buchwald SL. Palladium-Protein Oxidative Addition Complexes by Amine-Selective Acylation. Journal of the American Chemical Society. PMID 33319995 DOI: 10.1021/jacs.0c09180 |
0.318 |
|
2020 |
McCann SD, Reichert EC, Arrechea PL, Buchwald SL. Development of an Aryl Amination Catalyst with Broad Scope Guided by Consideration of Catalyst Stability. Journal of the American Chemical Society. 142: 15027-15037. PMID 32786769 DOI: 10.1021/Jacs.0C06139 |
0.5 |
|
2020 |
Link A, Zhou Y, Buchwald SL. CuH-Catalyzed Asymmetric Reductive Amidation of α,β-Unsaturated Carboxylic Acids. Organic Letters. 22: 5666-5670. PMID 32628019 DOI: 10.1021/Acs.Orglett.0C02064 |
0.408 |
|
2020 |
Dhanjee HH, Saebi A, Buslov I, Loftis AR, Buchwald SL, Pentelute BL. Correction to "Protein-Protein Cross-Coupling via Palladium-Protein Oxidative Addition Complexes from Cysteine Residues". Journal of the American Chemical Society. PMID 32603593 DOI: 10.1021/Jacs.0C06703 |
0.589 |
|
2020 |
Guo S, Zhu J, Buchwald SL. Enantioselective Synthesis of β-Amino Acid Derivatives Enabled by Ligand-Controlled Reversal of Hydrocupration Regiochemistry. Angewandte Chemie (International Ed. in English). PMID 32598506 DOI: 10.1002/Anie.202007005 |
0.357 |
|
2020 |
Zhang H, Ruiz-Castillo P, Schuppe AW, Buchwald SL. Improved Process for the Palladium-Catalyzed C-O Cross-Coupling of Secondary Alcohols. Organic Letters. PMID 32579375 DOI: 10.1021/Acs.Orglett.0C01668 |
0.411 |
|
2020 |
Mo Y, Lu Z, Rughoobur G, Patil P, Gershenfeld N, Akinwande AI, Buchwald SL, Jensen KF. Microfluidic electrochemistry for single-electron transfer redox-neutral reactions. Science (New York, N.Y.). 368: 1352-1357. PMID 32554592 DOI: 10.1126/Science.Aba3823 |
0.381 |
|
2020 |
Gribble MW, Liu RY, Buchwald SL. Evidence for Simultaneous Dearomatization of Two Aromatic Rings Under Mild Conditions in Cu(I)-Catalyzed Direct Asymmetric Dearomatization of Pyridine. Journal of the American Chemical Society. PMID 32453952 DOI: 10.1021/Jacs.0C04486 |
0.448 |
|
2020 |
Lu Z, Buchwald SL. The Enantioselective Preparation of Arenes with β-Stereogenic Centers: Confronting the 1,1-Disubstituted Olefin Problem Using CuH/Pd Cooperative Catalysis. Angewandte Chemie (International Ed. in English). PMID 32438497 DOI: 10.1002/Anie.202004414 |
0.541 |
|
2020 |
Ye Y, Kevlishvili I, Feng S, Liu P, Buchwald SL. Highly Enantioselective Synthesis of Indazoles with a C3-Quaternary Chiral Center Using CuH Catalysis. Journal of the American Chemical Society. PMID 32408745 DOI: 10.1021/Jacs.0C04286 |
0.461 |
|
2020 |
Liu RY, Buchwald SL. CuH-Catalyzed Olefin Functionalization: From Hydroamination to Carbonyl Addition. Accounts of Chemical Research. PMID 32401530 DOI: 10.1021/Acs.Accounts.0C00164 |
0.559 |
|
2020 |
Zhou Y, Zhou L, Jesikiewicz LT, Liu P, Buchwald SL. Synthesis of Pyrroles Through the CuH-Catalyzed Coupling of Enynes and Nitriles. Journal of the American Chemical Society. PMID 32395998 DOI: 10.1021/Jacs.0C03859 |
0.525 |
|
2020 |
Dhanjee HH, Saebi A, Buslov I, Loftis AR, Buchwald SL, Pentelute BL. Protein-Protein Cross-Coupling via Palladium-Protein Oxidative Addition Complexes from Cysteine Residues. Journal of the American Chemical Society. PMID 32364380 DOI: 10.1021/Jacs.0C03143 |
0.616 |
|
2020 |
Liu RY, Dennis JM, Buchwald SL. The Quest for the Ideal Base: Rational Design of a Nickel Precatalyst Enables Mild, Homogeneous C-N Cross-Coupling. Journal of the American Chemical Society. PMID 32040909 DOI: 10.1021/Jacs.0C00286 |
0.486 |
|
2020 |
Park BY, Pirnot MT, Buchwald SL. Visible Light-Mediated (Hetero)aryl Amination Using Ni(II) Salts and Photoredox Catalysis in Flow: A Synthesis of Tetracaine. The Journal of Organic Chemistry. PMID 31895983 DOI: 10.1021/Acs.Joc.9B03107 |
0.839 |
|
2019 |
Xu J, Liu RY, Yeung CS, Buchwald SL. Monophosphine Ligands Promote Pd-Catalyzed C-S Cross-Coupling Reactions at Room Temperature with Soluble Bases. Acs Catalysis. 9: 6461-6466. PMID 31929949 DOI: 10.1021/Acscatal.9B01913 |
0.489 |
|
2019 |
Ingoglia BT, Wagen CC, Buchwald SL. Biaryl Monophosphine Ligands in Palladium-Catalyzed C-N Coupling: An Updated User's Guide. Tetrahedron. 75: 4199-4211. PMID 31896889 DOI: 10.1016/J.Tet.2019.05.003 |
0.844 |
|
2019 |
Schuppe AW, Borrajo-Calleja GM, Buchwald SL. Enantioselective Olefin Hydrocyanation without Cyanide. Journal of the American Chemical Society. PMID 31687821 DOI: 10.1021/Jacs.9B10875 |
0.525 |
|
2019 |
Dennis JM, White NA, Liu RY, Buchwald SL. Pd-Catalyzed C-N Coupling Reactions Facilitated by Organic Bases: Mechanistic Investigation Leads to Enhanced Reactivity in the Arylation of Weakly Binding Amines. Acs Catalysis. 9: 3822-3830. PMID 31649828 DOI: 10.1021/Acscatal.9B00981 |
0.711 |
|
2019 |
Ichikawa S, Buchwald SL. Asymmetric Synthesis of γ-Amino Alcohols by Copper-Catalyzed Hydroamination. Organic Letters. 21: 8736-8739. PMID 31625750 DOI: 10.1021/Acs.Orglett.9B03356 |
0.358 |
|
2019 |
Li C, Shin K, Liu RY, Buchwald SL. Engaging Aldehydes in CuH-Catalyzed Reductive Coupling Reactions: Stereoselective Allylation with Unactivated 1,3-Diene Pronucleophiles. Angewandte Chemie (International Ed. in English). PMID 31552701 DOI: 10.1002/Anie.201911008 |
0.742 |
|
2019 |
Wagen CC, Ingoglia BT, Buchwald SL. Unexpected Formation of Hexasubstituted Arenes through a Twofold Palladium-Mediated Ligand Arylation. The Journal of Organic Chemistry. PMID 31512875 DOI: 10.1021/Acs.Joc.9B02091 |
0.818 |
|
2019 |
Bayeh-Romero L, Buchwald SL. Copper Hydride Catalyzed Enantioselective Synthesis of Axially Chiral 1,3-Disubstituted Allenes. Journal of the American Chemical Society. PMID 31423768 DOI: 10.1021/Jacs.9B07582 |
0.468 |
|
2019 |
Ichikawa S, Dai XJ, Buchwald SL. Regio- and Enantioselective Synthesis of 1,2-Diamine Derivatives by Copper-Catalyzed Hydroamination. Organic Letters. PMID 31099584 DOI: 10.1021/Acs.Orglett.9B01592 |
0.482 |
|
2019 |
Li C, Liu RY, Jesikiewicz LT, Yang Y, Liu P, Buchwald SL. CuH-Catalyzed Enantioselective Ketone Allylation with 1,3-Dienes: Scope, Mechanism, and Applications. Journal of the American Chemical Society. PMID 30817137 DOI: 10.1021/Jacs.9B01784 |
0.727 |
|
2019 |
Ye Y, Kim ST, Jeong J, Baik MH, Buchwald SL. CuH-Catalyzed Enantioselective Alkylation of Indole Derivatives with Ligand-Controlled Regiodivergence. Journal of the American Chemical Society. PMID 30696242 DOI: 10.1021/Jacs.8B11838 |
0.501 |
|
2019 |
Liu RY, Zhou Y, Yang Y, Buchwald SL. Enantioselective Allylation Using Allene, a Petroleum Cracking Byproduct. Journal of the American Chemical Society. PMID 30685967 DOI: 10.1021/Jacs.8B13907 |
0.497 |
|
2019 |
Uehling MR, King RP, Krska SW, Cernak T, Buchwald SL. Pharmaceutical diversification via palladium oxidative addition complexes. Science (New York, N.Y.). 363: 405-408. PMID 30679373 DOI: 10.1126/Science.Aac6153 |
0.703 |
|
2019 |
Dai XJ, Engl OD, León T, Buchwald SL. Catalytic Asymmetric Synthesis of α-Arylpyrrolidines and Benzo-fused Nitrogen Heterocycles. Angewandte Chemie (International Ed. in English). PMID 30659729 DOI: 10.1002/Anie.201814331 |
0.849 |
|
2019 |
Feng S, Hao H, Liu P, Buchwald SL. Diastereo- and Enantioselective CuH-Catalyzed Hydroamination of Strained Trisubstituted Alkenes Acs Catalysis. 10: 282-291. DOI: 10.1021/Acscatal.9B04871 |
0.447 |
|
2019 |
King RP, Buchwald SL. Synthesis of (MeCN)2Pd(CF3)OTs, a General Precursor to Palladium(II) Trifluoromethyl Complexes LPd(CF3)X Organometallics. 38: 3490-3493. DOI: 10.1021/Acs.Organomet.9B00516 |
0.455 |
|
2019 |
Baumgartner LM, Dennis JM, White NA, Buchwald SL, Jensen KF. Use of a Droplet Platform To Optimize Pd-Catalyzed C–N Coupling Reactions Promoted by Organic Bases Organic Process Research & Development. 23: 1594-1601. DOI: 10.1021/Acs.Oprd.9B00236 |
0.655 |
|
2019 |
Zhang C, Vinogradova EV, Spokoyny AM, Buchwald SL, Pentelute BL. Arylierungschemie für die Biokonjugation Angewandte Chemie. 131: 4860-4892. DOI: 10.1002/Ange.201806009 |
0.678 |
|
2019 |
Huang W, Einzinger M, Maurano A, Zhu T, Tiepelt J, Yu C, Chae HS, Van Voorhis T, Baldo MA, Buchwald SL. Large Increase in External Quantum Efficiency by Dihedral Angle Tuning in a Sky‐Blue Thermally Activated Delayed Fluorescence Emitter Advanced Optical Materials. 7: 1900476. DOI: 10.1002/Adom.201900476 |
0.597 |
|
2019 |
Wang H, Buchwald SL. Copper‐Catalyzed, Enantioselective Hydrofunctionalization of Alkenes Organic Reactions. 121-206. DOI: 10.1002/0471264180.Or100.03 |
0.489 |
|
2018 |
Pentelute B, Zhang C, Vinogradova E, Spokoyny A, Buchwald S. Arylation Chemistry for Bioconjugation. Angewandte Chemie (International Ed. in English). PMID 30399206 DOI: 10.1002/Anie.201806009 |
0.794 |
|
2018 |
Cohen DT, Zhang C, Fadzen CM, Mijalis AJ, Hie L, Johnson KD, Shriver Z, Plante O, Miller SJ, Buchwald SL, Pentelute BL. A chemoselective strategy for late-stage functionalization of complex small molecules with polypeptides and proteins. Nature Chemistry. PMID 30397320 DOI: 10.1038/S41557-018-0154-0 |
0.735 |
|
2018 |
Guo S, Yang JC, Buchwald SL. A Practical Electrophilic Nitrogen Source for the Synthesis of Chiral Primary Amines by Copper-Catalyzed Hydroamination. Journal of the American Chemical Society. PMID 30371077 DOI: 10.1021/Jacs.8B10564 |
0.468 |
|
2018 |
Liu RY, Buchwald SL. Copper-Catalyzed Enantioselective Hydroamination of Alkenes. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 95: 80-96. PMID 30287975 DOI: 10.15227/Orgsyn.095.0080 |
0.442 |
|
2018 |
Thomas AA, Speck K, Kevlishvili I, Lu Z, Liu P, Buchwald SL. Mechanistically Guided Design of Ligands that Significantly Improve the Efficiency of CuH-Catalyzed Hydroamination Reactions. Journal of the American Chemical Society. PMID 30244567 DOI: 10.1021/Jacs.8B09565 |
0.43 |
|
2018 |
Buchwald SL, Khan RKM, Zhao Y, Scully T. Catalytic Arylhydroxylation of Dehydroalanine in Continuous Flow for Simple Access to Unnatural Amino Acids. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30102444 DOI: 10.1002/Chem.201804094 |
0.41 |
|
2018 |
Ichikawa S, Zhu S, Buchwald SL. A Modified System for the Synthesis of Enantioenriched N-Arylamines through Copper-Catalyzed Hydroamination. Angewandte Chemie (International Ed. in English). PMID 29847002 DOI: 10.1002/Anie.201803026 |
0.756 |
|
2018 |
Shi SL, Wong ZL, Buchwald SL. Addendum: Copper-catalysed enantioselective stereodivergent synthesis of amino alcohols. Nature. PMID 29795353 DOI: 10.1038/S41586-018-0112-4 |
0.691 |
|
2018 |
Tsai EY, Liu RY, Yang Y, Buchwald SL. Correction to "A Regio- and Enantioselective CuH-Catalyzed Ketone Allylation with Terminal Allenes". Journal of the American Chemical Society. PMID 29737849 DOI: 10.1021/Jacs.8B04366 |
0.836 |
|
2018 |
Zhou Y, Engl OD, Bandar JS, Chant ED, Buchwald SL. CuH-Catalyzed Asymmetric Hydroamidation of Vinylarenes. Angewandte Chemie (International Ed. in English). PMID 29660768 DOI: 10.1002/Anie.201802797 |
0.848 |
|
2018 |
Gribble MW, Guo S, Buchwald SL. Asymmetric Cu-Catalyzed 1,4-Dearomatization of Pyridines and Pyridazines without Preactivation of the Heterocycle or Nucleophile. Journal of the American Chemical Society. PMID 29609461 DOI: 10.1021/Jacs.8B02568 |
0.509 |
|
2018 |
Dennis JM, White NA, Liu RY, Buchwald SL. Breaking the Base Barrier: An Electron-Deficient Palladium Catalyst Enables the Use of a Common, Soluble Base in C-N Coupling. Journal of the American Chemical Society. PMID 29529363 DOI: 10.1021/Jacs.8B01696 |
0.699 |
|
2018 |
Zhang H, Ruiz-Castillo P, Buchwald SL. Palladium-Catalyzed C-O Cross-Coupling of Primary Alcohols. Organic Letters. PMID 29474078 DOI: 10.1021/Acs.Orglett.8B00325 |
0.437 |
|
2018 |
Kubota K, Dai P, Pentelute BL, Buchwald SL. Palladium Oxidative Addition Complexes for Peptide and Protein Crosslinking. Journal of the American Chemical Society. PMID 29406701 DOI: 10.1021/Jacs.8B00172 |
0.616 |
|
2018 |
Tsai E, Liu RY, Yang Y, Buchwald SL. A Regio- and Enantioselective CuH-Catalyzed Ketone Allylation with Terminal Allenes. Journal of the American Chemical Society. PMID 29376366 DOI: 10.1021/Jacs.7B12271 |
0.841 |
|
2018 |
Liu RY, Bae M, Buchwald SL. Mechanistic Insight Facilitates Discovery of a Mild and Efficient Copper-Catalyzed Dehydration of Primary Amides to Nitriles Using Hydrosilanes. Journal of the American Chemical Society. PMID 29353477 DOI: 10.1021/Jacs.8B00643 |
0.453 |
|
2018 |
Zhou Y, Bandar JS, Liu RY, Buchwald SL. CuH-Catalyzed Asymmetric Reduction of α,β-Unsaturated Carboxylic Acids to β-Chiral Aldehydes. Journal of the American Chemical Society. PMID 29283578 DOI: 10.1021/Jacs.7B12260 |
0.771 |
|
2018 |
Huang W, Einzinger M, Zhu T, Chae HS, Jeon S, Ihn S, Sim M, Kim S, Su M, Teverovskiy G, Wu T, Van Voorhis T, Swager TM, Baldo MA, Buchwald SL. Molecular Design of Deep Blue Thermally Activated Delayed Fluorescence Materials Employing a Homoconjugative Triptycene Scaffold and Dihedral Angle Tuning Chemistry of Materials. 30: 1462-1466. DOI: 10.1021/Acs.Chemmater.7B03490 |
0.753 |
|
2017 |
Rojas AJ, Zhang C, Vinogradova EV, Buchwald NH, Reilly J, Pentelute BL, Buchwald SL. Divergent unprotected peptide macrocyclisation by palladium-mediated cysteine arylation. Chemical Science. 8: 4257-4263. PMID 29081961 DOI: 10.1039/C6Sc05454D |
0.781 |
|
2017 |
Lu G, Liu RY, Yang Y, Fang C, Lambrecht DS, Buchwald SL, Liu P. Ligand-Substrate Dispersion Facilitates the Copper-Catalyzed Hydroamination of Unactivated Olefins. Journal of the American Chemical Society. PMID 29064694 DOI: 10.1021/Jacs.7B07373 |
0.459 |
|
2017 |
Rojas AJ, Pentelute BL, Buchwald SL. Water-Soluble Palladium Reagents for Cysteine S-Arylation under Ambient Aqueous Conditions. Organic Letters. PMID 28777001 DOI: 10.1021/Acs.Orglett.7B01911 |
0.775 |
|
2017 |
Zhang H, Buchwald SL. Palladium-Catalyzed Negishi Coupling of α-CF3 Oxiranyl Zincate: Access to Chiral CF3-substituted Benzylic Tertiary Alcohols. Journal of the American Chemical Society. PMID 28753004 DOI: 10.1021/Jacs.7B06630 |
0.39 |
|
2017 |
Olsen EPK, Arrechea PL, Buchwald SL. Mechanistic Insight Leads to a Ligand That Facilitates the Pd-Catalyzed Formation of 2-(Hetero)Arylaminooxazoles and 4-(Hetero)Arylaminothiazoles. Angewandte Chemie (International Ed. in English). PMID 28605135 DOI: 10.1002/Anie.201705525 |
0.45 |
|
2017 |
Wang H, Yang JC, Buchwald SL. CuH-Catalyzed Regioselective Intramolecular Hydroamination for the Synthesis of Alkyl-Substituted Chiral Aziridines. Journal of the American Chemical Society. PMID 28594548 DOI: 10.1021/Jacs.7B04816 |
0.494 |
|
2017 |
Zhou Y, Bandar JS, Buchwald SL. Enantioselective CuH-Catalyzed Hydroacylation Employing Unsaturated Carboxylic Acids as Aldehyde Surrogates. Journal of the American Chemical Society. 139: 8126-8129. PMID 28565905 DOI: 10.1021/Jacs.7B04937 |
0.803 |
|
2017 |
Friis SD, Pirnot MT, Dupuis LN, Buchwald SL. A Dual Palladium and Copper Hydride Catalyzed Approach for Alkyl-Aryl Cross-Coupling of Aryl Halides and Olefins. Angewandte Chemie (International Ed. in English). 56: 7242-7246. PMID 28510287 DOI: 10.1002/Anie.201703400 |
0.844 |
|
2017 |
Zhao W, Lee HG, Buchwald SL, Hooker JM. Direct (11)CN-Labeling of Unprotected Peptides via Palladium-Mediated Sequential Cross-Coupling Reactions. Journal of the American Chemical Society. 139: 7152-7155. PMID 28502164 DOI: 10.1021/Jacs.7B02761 |
0.613 |
|
2017 |
Ingoglia BT, Buchwald SL. Oxidative Addition Complexes as Precatalysts for Cross-Coupling Reactions Requiring Extremely Bulky Biarylphosphine Ligands. Organic Letters. 19: 2853-2856. PMID 28498667 DOI: 10.1021/Acs.Orglett.7B01082 |
0.824 |
|
2017 |
Lee HG, Lautrette G, Pentelute BL, Buchwald SL. Palladium-Mediated Arylation of Lysine in Unprotected Peptides. Angewandte Chemie (International Ed. in English). 56: 3177-3181. PMID 28206688 DOI: 10.1002/Anie.201611202 |
0.714 |
|
2017 |
Gribble MW, Pirnot MT, Bandar JS, Liu RY, Buchwald SL. Asymmetric Copper Hydride-Catalyzed Markovnikov Hydrosilylation of Vinylarenes and Vinyl Heterocycles. Journal of the American Chemical Society. 139: 2192-2195. PMID 28117996 DOI: 10.1021/Jacs.6B13029 |
0.828 |
|
2016 |
Reizman BJ, Wang YM, Buchwald SL, Jensen KF. Suzuki-Miyaura cross-coupling optimization enabled by automated feedback. Reaction Chemistry & Engineering. 1: 658-666. PMID 27928513 DOI: 10.1039/C6Re00153J |
0.536 |
|
2016 |
Ye Y, Takada T, Buchwald SL. Palladium-Catalyzed Fluorination of Cyclic Vinyl Triflates: Effect of TESCF3 as an Additive. Angewandte Chemie (International Ed. in English). 55: 15559-15563. PMID 27862732 DOI: 10.1002/Anie.201608927 |
0.528 |
|
2016 |
Liu RY, Yang Y, Buchwald SL. Regiodivergent and Diastereoselective CuH-Catalyzed Allylation of Imines with Terminal Allenes. Angewandte Chemie (International Ed. in English). 55: 14077-14080. PMID 27723269 DOI: 10.1002/Anie.201608446 |
0.51 |
|
2016 |
Ruiz-Castillo P, Buchwald SL. Applications of Palladium-Catalyzed C-N Cross-Coupling Reactions. Chemical Reviews. 116: 12564-12649. PMID 27689804 DOI: 10.1021/Acs.Chemrev.6B00512 |
0.52 |
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2016 |
Sather AC, Buchwald SL. The Evolution of Pd(0)/Pd(II)-Catalyzed Aromatic Fluorination. Accounts of Chemical Research. 49: 2146-2157. PMID 27656765 DOI: 10.1021/Acs.Accounts.6B00247 |
0.789 |
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2016 |
Arrechea PL, Buchwald SL. Biaryl Phosphine Based Pd(II) Amido Complexes: The Effect of Ligand Structure on Reductive Elimination. Journal of the American Chemical Society. 138: 12486-93. PMID 27562724 DOI: 10.1021/Jacs.6B05990 |
0.467 |
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2016 |
Park NH, Senter TJ, Buchwald SL. Rapid Synthesis of Aryl Fluorides in Continuous Flow through the Balz-Schiemann Reaction. Angewandte Chemie (International Ed. in English). 55: 11907-11. PMID 27558308 DOI: 10.1002/Anie.201606601 |
0.841 |
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2016 |
King SM, Buchwald SL. Development of a Method for the N-Arylation of Amino Acid Esters with Aryl Triflates. Organic Letters. 18: 4128-31. PMID 27498618 DOI: 10.1021/Acs.Orglett.6B02082 |
0.72 |
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2016 |
Huang W, Buchwald SL. Palladium-Catalyzed N-Arylation of Iminodibenzyls and Iminostilbenes with Aryl- and Heteroaryl Halides. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 14186-9. PMID 27481439 DOI: 10.1002/Chem.201603449 |
0.741 |
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2016 |
Roesner S, Buchwald SL. Continuous-Flow Synthesis of Biaryls by Negishi Cross-Coupling of Fluoro- and Trifluoromethyl-Substituted (Hetero)arenes. Angewandte Chemie (International Ed. in English). 55: 10463-7. PMID 27456275 DOI: 10.1002/Anie.201605584 |
0.77 |
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2016 |
Yang Y, Perry IB, Buchwald SL. Copper-Catalyzed Enantioselective Addition of Styrene-Derived Nucleophiles to Imines Enabled by Ligand-Controlled Chemoselective Hydrocupration. Journal of the American Chemical Society. 138: 9787-90. PMID 27454393 DOI: 10.1021/Jacs.6B06299 |
0.52 |
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2016 |
Friis SD, Pirnot MT, Buchwald SL. Asymmetric Hydroarylation of Vinylarenes Using a Synergistic Combination of CuH and Pd Catalysis. Journal of the American Chemical Society. 138: 8372-5. PMID 27346525 DOI: 10.1021/Jacs.6B04566 |
0.827 |
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2016 |
Corcoran EB, Pirnot MT, Lin S, Dreher SD, DiRocco DA, Davies IW, Buchwald SL, MacMillan DW. Aryl amination using ligand-free Ni(II) salts and photoredox catalysis. Science (New York, N.Y.). 353: 279-83. PMID 27338703 DOI: 10.1126/Science.Aag0209 |
0.815 |
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2016 |
Yang Y, Perry IB, Lu G, Liu P, Buchwald SL. Copper-catalyzed asymmetric addition of olefin-derived nucleophiles to ketones. Science (New York, N.Y.). 353: 144-50. PMID 27284169 DOI: 10.1126/Science.Aaf7720 |
0.503 |
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2016 |
Bandar JS, Ascic E, Buchwald SL. Enantioselective CuH-Catalyzed Reductive Coupling of Aryl Alkenes and Activated Carboxylic Acids. Journal of the American Chemical Society. 138: 5821-4. PMID 27121395 DOI: 10.1021/Jacs.6B03086 |
0.809 |
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2016 |
Smith SM, Buchwald SL. Regioselective 2-Amination of Polychloropyrimidines. Organic Letters. 18: 2180-3. PMID 27082704 DOI: 10.1021/Acs.Orglett.6B00799 |
0.464 |
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2016 |
Wang YM, Buchwald SL. Enantioselective CuH-Catalyzed Hydroallylation of Vinylarenes. Journal of the American Chemical Society. 138: 5024-7. PMID 27042864 DOI: 10.1021/Jacs.6B02527 |
0.547 |
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2016 |
Shi SL, Wong ZL, Buchwald SL. Copper-catalysed enantioselective stereodivergent synthesis of amino alcohols. Nature. 532: 353-6. PMID 27018656 DOI: 10.1038/Nature17191 |
0.71 |
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2016 |
Zhu S, Niljianskul N, Buchwald SL. A direct approach to amines with remote stereocentres by enantioselective CuH-catalysed reductive relay hydroamination. Nature Chemistry. 8: 144-50. PMID 26791897 DOI: 10.1038/Nchem.2418 |
0.823 |
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2016 |
Yang JC, Niu D, Karsten BP, Lima F, Buchwald SL. Use of a "Catalytic" Cosolvent, N,N-Dimethyl Octanamide, Allows the Flow Synthesis of Imatinib with no Solvent Switch. Angewandte Chemie (International Ed. in English). 55: 2531-5. PMID 26756279 DOI: 10.1002/Anie.201509922 |
0.694 |
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2016 |
Bhonde VR, O'Neill BT, Buchwald SL. An Improved System for the Aqueous Lipshutz-Negishi Cross-Coupling of Alkyl Halides with Aryl Electrophiles. Angewandte Chemie (International Ed. in English). 55: 1849-53. PMID 26676401 DOI: 10.1002/Anie.201509341 |
0.477 |
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2016 |
Pirnot MT, Wang YM, Buchwald SL. Copper Hydride Catalyzed Hydroamination of Alkenes and Alkynes. Angewandte Chemie (International Ed. in English). 55: 48-57. PMID 26661678 DOI: 10.1002/Anie.201507594 |
0.832 |
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2016 |
Liu RY, Yang Y, Buchwald SL. Regio- and Diastereoselective Copper-Catalyzed Allylation of Imines Synfacts. 12: 1258-1258. DOI: 10.1055/S-0036-1589695 |
0.452 |
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2016 |
Yang Y, Perry IB, Lu G, Liu P, Buchwald SL. ChemInform Abstract: Copper-Catalyzed Asymmetric Addition of Olefin-Derived Nucleophiles to Ketones. Cheminform. 47. DOI: 10.1002/CHIN.201639024 |
0.38 |
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2015 |
Milner PJ, Yang Y, Buchwald SL. In-Depth Assessment of the Palladium-Catalyzed Fluorination of Five-Membered Heteroaryl Bromides. Organometallics. 34: 4775-4780. PMID 27056379 DOI: 10.1021/Acs.Organomet.5B00631 |
0.736 |
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2015 |
Bandar JS, Pirnot MT, Buchwald SL. Mechanistic Studies Lead to Dramatically Improved Reaction Conditions for the Cu-Catalyzed Asymmetric Hydroamination of Olefins. Journal of the American Chemical Society. 137: 14812-8. PMID 26522837 DOI: 10.1021/Jacs.5B10219 |
0.84 |
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2015 |
Vinogradova EV, Zhang C, Spokoyny AM, Pentelute BL, Buchwald SL. Organometallic palladium reagents for cysteine bioconjugation. Nature. 526: 687-91. PMID 26511579 DOI: 10.1038/Nature15739 |
0.829 |
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2015 |
Sather AC, Lee HG, De La Rosa VY, Yang Y, Müller P, Buchwald SL. A Fluorinated Ligand Enables Room-Temperature and Regioselective Pd-Catalyzed Fluorination of Aryl Triflates and Bromides. Journal of the American Chemical Society. 137: 13433-8. PMID 26413908 DOI: 10.1021/Jacs.5B09308 |
0.816 |
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2015 |
Sather AC, Lee HG, Colombe JR, Zhang A, Buchwald SL. Dosage delivery of sensitive reagents enables glove-box-free synthesis. Nature. 524: 208-11. PMID 26268191 DOI: 10.1038/Nature14654 |
0.812 |
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2015 |
Wang YM, Bruno NC, Placeres ÁL, Zhu S, Buchwald SL. Enantioselective Synthesis of Carbo- and Heterocycles through a CuH-Catalyzed Hydroalkylation Approach. Journal of the American Chemical Society. 137: 10524-7. PMID 26256576 DOI: 10.1021/Jacs.5B07061 |
0.832 |
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2015 |
Cohen DT, Zhang C, Pentelute BL, Buchwald SL. An Umpolung Approach for the Chemoselective Arylation of Selenocysteine in Unprotected Peptides. Journal of the American Chemical Society. 137: 9784-7. PMID 26225900 DOI: 10.1021/Jacs.5B05447 |
0.732 |
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2015 |
Niu D, Buchwald SL. Design of Modified Amine Transfer Reagents Allows the Synthesis of α-Chiral Secondary Amines via CuH-Catalyzed Hydroamination. Journal of the American Chemical Society. 137: 9716-21. PMID 26144542 DOI: 10.1021/Jacs.5B05446 |
0.64 |
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2015 |
Yang Y, Shi SL, Niu D, Liu P, Buchwald SL. ORGANIC CHEMISTRY. Catalytic asymmetric hydroamination of unactivated internal olefins to aliphatic amines. Science (New York, N.Y.). 349: 62-6. PMID 26138973 DOI: 10.1126/Science.Aab3753 |
0.795 |
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2015 |
Zhu R, Buchwald SL. Versatile Enantioselective Synthesis of Functionalized Lactones via Copper-Catalyzed Radical Oxyfunctionalization of Alkenes. Journal of the American Chemical Society. 137: 8069-77. PMID 26070105 DOI: 10.1021/Jacs.5B04821 |
0.614 |
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2015 |
Colombe JR, DeBergh JR, Buchwald SL. Synthesis of Heteroaryl Sulfonamides from Organozinc Reagents and 2,4,6-Trichlorophenyl Chlorosulfate. Organic Letters. 17: 3170-3. PMID 26065317 DOI: 10.1021/Acs.Orglett.5B01540 |
0.488 |
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2015 |
Park NH, Vinogradova EV, Surry DS, Buchwald SL. Design of New Ligands for the Palladium-Catalyzed Arylation of α-Branched Secondary Amines. Angewandte Chemie (International Ed. in English). 54: 8259-62. PMID 26032920 DOI: 10.1002/Anie.201502626 |
0.687 |
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2015 |
Ascic E, Buchwald SL. Highly diastereo- and enantioselective CuH-catalyzed synthesis of 2,3-disubstituted indolines. Journal of the American Chemical Society. 137: 4666-9. PMID 25826004 DOI: 10.1021/Jacs.5B02316 |
0.504 |
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2015 |
Ruiz-Castillo P, Blackmond DG, Buchwald SL. Rational ligand design for the arylation of hindered primary amines guided by reaction progress kinetic analysis. Journal of the American Chemical Society. 137: 3085-92. PMID 25651374 DOI: 10.1021/Ja512903G |
0.471 |
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2015 |
Lee HG, Milner PJ, Placzek MS, Buchwald SL, Hooker JM. Virtually instantaneous, room-temperature [(11)C]-cyanation using biaryl phosphine Pd(0) complexes. Journal of the American Chemical Society. 137: 648-51. PMID 25565277 DOI: 10.1021/Ja512115S |
0.779 |
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2015 |
Cohen DT, Buchwald SL. Mild palladium-catalyzed cyanation of (hetero)aryl halides and triflates in aqueous media. Organic Letters. 17: 202-5. PMID 25555140 DOI: 10.1021/Ol5032359 |
0.673 |
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2015 |
Shi SL, Buchwald SL. Copper-catalysed selective hydroamination reactions of alkynes. Nature Chemistry. 7: 38-44. PMID 25515888 DOI: 10.1038/Nchem.2131 |
0.763 |
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2015 |
Shi SL, Buchwald SL. Palladium-catalyzed intramolecular C-H difluoroalkylation: synthesis of substituted 3,3-difluoro-2-oxindoles. Angewandte Chemie (International Ed. in English). 54: 1646-50. PMID 25476241 DOI: 10.1002/Anie.201410471 |
0.751 |
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2015 |
Niljianskul N, Zhu S, Buchwald SL. Enantioselective synthesis of α-aminosilanes by copper-catalyzed hydroamination of vinylsilanes. Angewandte Chemie (International Ed. in English). 54: 1638-41. PMID 25475991 DOI: 10.1002/Anie.201410326 |
0.84 |
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2015 |
Chen M, Ichikawa S, Buchwald SL. Rapid and efficient copper-catalyzed Finkelstein reaction of (hetero)aromatics under continuous-flow conditions. Angewandte Chemie (International Ed. in English). 54: 263-6. PMID 25378244 DOI: 10.1002/Anie.201409595 |
0.573 |
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2015 |
Wang Y-, Bruno NC, Placeres ÁL, Zhu S, Buchwald SL. Copper-Catalyzed Enantioselective Synthesis of Carbo- and Heterocycles Synfacts. 11: 1167-1167. DOI: 10.1055/S-0035-1560692 |
0.837 |
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2015 |
Cohen DT, Zhang C, Pentelute BL, Buchwald SL. An Umpolung Approach for the Chemoselective Arylation of Selenocysteine in Unprotected Peptides Journal of the American Chemical Society. 137: 9784-9787. DOI: 10.1021/jacs.5b05447 |
0.647 |
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2015 |
Milner PJ, Yang Y, Buchwald SL. Correction to In-Depth Assessment of the Palladium-Catalyzed Fluorination of Five-Membered Heteroaryl Bromides Organometallics. 34: 5361-5361. DOI: 10.1021/Acs.Organomet.5B00881 |
0.401 |
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2015 |
Milner PJ, Yang Y, Buchwald SL. In-Depth Assessment of the Palladium-Catalyzed Fluorination of Five-Membered Heteroaryl Bromides Organometallics. 34: 4775-4780. DOI: 10.1021/acs.organomet.5b00631 |
0.672 |
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2015 |
Yang Y, Shi S, Niu D, Liu P, Buchwald SL. ChemInform Abstract: Catalytic Asymmetric Hydroamination of Unactivated Internal Olefins to Aliphatic Amines. Cheminform. 46: no-no. DOI: 10.1002/chin.201549026 |
0.602 |
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2015 |
Shi S, Buchwald SL. ChemInform Abstract: Palladium-Catalyzed Intramolecular C-H Difluoroalkylation: Synthesis of Substituted 3,3-Difluoro-2-oxindoles. Cheminform. 46: no-no. DOI: 10.1002/chin.201524131 |
0.319 |
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2015 |
Pirnot MT, Wang Y, Buchwald SL. Kupferhydrid-katalysierte Hydroaminierung von Alkenen und Alkinen Angewandte Chemie. 128: 48-57. DOI: 10.1002/Ange.201507594 |
0.751 |
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2014 |
Lee HG, Milner PJ, Colvin MT, Andreas L, Buchwald SL. Structure and Reactivity of [(L•Pd)n•(1,5-cyclooctadiene)] (n=1-2) Complexes Bearing Biaryl Phosphine Ligands. Inorganica Chimica Acta. 422: 188-192. PMID 25346547 DOI: 10.1016/J.Ica.2014.06.008 |
0.75 |
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2014 |
Zhu S, Buchwald SL. Enantioselective CuH-catalyzed anti-Markovnikov hydroamination of 1,1-disubstituted alkenes. Journal of the American Chemical Society. 136: 15913-6. PMID 25339089 DOI: 10.1021/Ja509786V |
0.751 |
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2014 |
Milner PJ, Kinzel T, Zhang Y, Buchwald SL. Studying regioisomer formation in the Pd-catalyzed fluorination of aryl triflates by deuterium labeling. Journal of the American Chemical Society. 136: 15757-66. PMID 25299957 DOI: 10.1021/Ja509144R |
0.697 |
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2014 |
Yang Y, Niedermann K, Han C, Buchwald SL. Highly selective palladium-catalyzed cross-coupling of secondary alkylzinc reagents with heteroaryl halides. Organic Letters. 16: 4638-41. PMID 25153332 DOI: 10.1021/Ol502230P |
0.665 |
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2014 |
Friis SD, Skrydstrup T, Buchwald SL. Mild Pd-catalyzed aminocarbonylation of (hetero)aryl bromides with a palladacycle precatalyst. Organic Letters. 16: 4296-9. PMID 25090373 DOI: 10.1021/Ol502014B |
0.467 |
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2014 |
Ernst JB, Tay NE, Jui NT, Buchwald SL. Regioselective synthesis of benzimidazolones via cascade C-N coupling of monosubstituted ureas. Organic Letters. 16: 3844-6. PMID 24971635 DOI: 10.1021/Ol501531Q |
0.768 |
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2014 |
Yang Y, Buchwald SL. Copper-catalyzed regioselective ortho C-H cyanation of vinylarenes. Angewandte Chemie (International Ed. in English). 53: 8677-81. PMID 24801708 DOI: 10.1002/Anie.201402449 |
0.46 |
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2014 |
Cheung CW, Buchwald SL. Palladium-catalyzed hydroxylation of aryl and heteroaryl halides enabled by the use of a palladacycle precatalyst. The Journal of Organic Chemistry. 79: 5351-8. PMID 24762125 DOI: 10.1021/Jo500662S |
0.557 |
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2014 |
Bruno NC, Niljianskul N, Buchwald SL. N-substituted 2-aminobiphenylpalladium methanesulfonate precatalysts and their use in C-C and C-N cross-couplings. The Journal of Organic Chemistry. 79: 4161-6. PMID 24724692 DOI: 10.1021/Jo500355K |
0.809 |
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2014 |
Vinogradova EV, Müller P, Buchwald SL. Structural reevaluation of the electrophilic hypervalent iodine reagent for trifluoromethylthiolation supported by the crystalline sponge method for X-ray analysis. Angewandte Chemie (International Ed. in English). 53: 3125-8. PMID 24677728 DOI: 10.1002/Anie.201310897 |
0.548 |
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2014 |
Zhu Y, Buchwald SL. Ligand-controlled asymmetric arylation of aliphatic α-amino anion equivalents. Journal of the American Chemical Society. 136: 4500-3. PMID 24621247 DOI: 10.1021/Ja501560X |
0.577 |
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2014 |
Lee HG, Milner PJ, Buchwald SL. Pd-catalyzed nucleophilic fluorination of aryl bromides. Journal of the American Chemical Society. 136: 3792-5. PMID 24559304 DOI: 10.1021/Ja5009739 |
0.801 |
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2014 |
Su M, Hoshiya N, Buchwald SL. Palladium-catalyzed amination of unprotected five-membered heterocyclic bromides. Organic Letters. 16: 832-5. PMID 24417224 DOI: 10.1021/Ol4035947 |
0.675 |
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2014 |
Park NH, Teverovskiy G, Buchwald SL. Development of an air-stable nickel precatalyst for the amination of aryl chlorides, sulfamates, mesylates, and triflates. Organic Letters. 16: 220-3. PMID 24283652 DOI: 10.1021/Ol403209K |
0.838 |
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2014 |
Lautens M, Petrone DA, Zhu Y, Buchwald SL. Synthesis of Enantioenriched Amines via an Asymmetric Palladium-Catalyzed Arylation Synfacts. 10: 716-716. DOI: 10.1055/S-0034-1378290 |
0.555 |
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2014 |
Shi S, Buchwald SL. Erratum: Copper-catalysed selective hydroamination reactions of alkynes Nature Chemistry. 7: 178-178. DOI: 10.1038/Nchem.2167 |
0.69 |
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2014 |
Yang Y, Buchwald SL. Copper-Catalyzed RegioselectiveorthoCH Cyanation of Vinylarenes Angewandte Chemie. 126: 8677-8681. DOI: 10.1002/Ange.201402449 |
0.368 |
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2013 |
Yang Y, Mustard TJ, Cheong PH, Buchwald SL. Palladium-catalyzed completely linear-selective Negishi cross-coupling of allylzinc halides with aryl and vinyl electrophiles. Angewandte Chemie (International Ed. in English). 52: 14098-102. PMID 24353232 DOI: 10.1002/Anie.201308585 |
0.696 |
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2013 |
Tardiff DF, Jui NT, Khurana V, Tambe MA, Thompson ML, Chung CY, Kamadurai HB, Kim HT, Lancaster AK, Caldwell KA, Caldwell GA, Rochet JC, Buchwald SL, Lindquist S. Yeast reveal a "druggable" Rsp5/Nedd4 network that ameliorates α-synuclein toxicity in neurons. Science (New York, N.Y.). 342: 979-83. PMID 24158909 DOI: 10.1126/Science.1245321 |
0.665 |
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2013 |
Chung CY, Khurana V, Auluck PK, Tardiff DF, Mazzulli JR, Soldner F, Baru V, Lou Y, Freyzon Y, Cho S, Mungenast AE, Muffat J, Mitalipova M, Pluth MD, Jui NT, ... ... Buchwald SL, et al. Identification and rescue of α-synuclein toxicity in Parkinson patient-derived neurons. Science (New York, N.Y.). 342: 983-7. PMID 24158904 DOI: 10.1126/Science.1245296 |
0.697 |
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2013 |
Colombe JR, Bernhardt S, Stathakis C, Buchwald SL, Knochel P. Synthesis of solid 2-pyridylzinc reagents and their application in Negishi reactions. Organic Letters. 15: 5754-7. PMID 24156393 DOI: 10.1021/Ol402798Z |
0.444 |
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2013 |
Lee HG, Milner PJ, Buchwald SL. An improved catalyst system for the Pd-catalyzed fluorination of (hetero)aryl triflates. Organic Letters. 15: 5602-5. PMID 24138611 DOI: 10.1021/Ol402859K |
0.789 |
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2013 |
Zhu R, Buchwald SL. Enantioselective functionalization of radical intermediates in redox catalysis: copper-catalyzed asymmetric oxytrifluoromethylation of alkenes. Angewandte Chemie (International Ed. in English). 52: 12655-8. PMID 24133010 DOI: 10.1002/Anie.201307790 |
0.563 |
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2013 |
Zhu S, Niljianskul N, Buchwald SL. Enantio- and regioselective CuH-catalyzed hydroamination of alkenes. Journal of the American Chemical Society. 135: 15746-9. PMID 24106781 DOI: 10.1021/Ja4092819 |
0.833 |
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2013 |
Chen M, Buchwald SL. Rapid and efficient trifluoromethylation of aromatic and heteroaromatic compounds using potassium trifluoroacetate enabled by a flow system. Angewandte Chemie (International Ed. in English). 52: 11628-31. PMID 24038907 DOI: 10.1002/Anie.201306094 |
0.536 |
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2013 |
Jui NT, Buchwald SL. Cascade palladium catalysis: a predictable and selectable regiocontrolled synthesis of N-arylbenzimidazoles. Angewandte Chemie (International Ed. in English). 52: 11624-7. PMID 24038854 DOI: 10.1002/Anie.201306007 |
0.747 |
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2013 |
Oberli MA, Buchwald SL. Correction to A General Method for Suzuki–Miyaura Coupling Reactions Using Lithium Triisopropyl Borates Organic Letters. 15: 2892-2892. PMID 23956687 DOI: 10.1021/Ol401288Q |
0.41 |
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2013 |
Senecal TD, Shu W, Buchwald SL. A general, practical palladium-catalyzed cyanation of (hetero)aryl chlorides and bromides. Angewandte Chemie (International Ed. in English). 52: 10035-9. PMID 23934947 DOI: 10.1002/Anie.201304188 |
0.829 |
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2013 |
Düfert MA, Billingsley KL, Buchwald SL. Suzuki-Miyaura cross-coupling of unprotected, nitrogen-rich heterocycles: substrate scope and mechanistic investigation. Journal of the American Chemical Society. 135: 12877-85. PMID 23909907 DOI: 10.1021/Ja4064469 |
0.788 |
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2013 |
Cheung CW, Buchwald SL. Mild and general palladium-catalyzed synthesis of methyl aryl ethers enabled by the use of a palladacycle precatalyst. Organic Letters. 15: 3998-4001. PMID 23883393 DOI: 10.1021/Ol401796V |
0.529 |
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2013 |
DeBergh JR, Niljianskul N, Buchwald SL. Synthesis of aryl sulfonamides via palladium-catalyzed chlorosulfonylation of arylboronic acids. Journal of the American Chemical Society. 135: 10638-41. PMID 23837740 DOI: 10.1021/Ja405949A |
0.838 |
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2013 |
Yang Y, Buchwald SL. Ligand-controlled palladium-catalyzed regiodivergent Suzuki-Miyaura cross-coupling of allylboronates and aryl halides. Journal of the American Chemical Society. 135: 10642-5. PMID 23837686 DOI: 10.1021/Ja405950C |
0.511 |
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2013 |
Cheung CW, Surry DS, Buchwald SL. Mild and highly selective palladium-catalyzed monoarylation of ammonia enabled by the use of bulky biarylphosphine ligands and palladacycle precatalysts. Organic Letters. 15: 3734-7. PMID 23815096 DOI: 10.1021/Ol401612C |
0.407 |
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2013 |
Bruno NC, Buchwald SL. Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands. Organic Letters. 15: 2876-9. PMID 23675976 DOI: 10.1021/Ol401208T |
0.838 |
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2013 |
Bruno NC, Tudge MT, Buchwald SL. Design and Preparation of New Palladium Precatalysts for C-C and C-N Cross-Coupling Reactions. Chemical Science. 4: 916-920. PMID 23667737 DOI: 10.1039/C2Sc20903A |
0.817 |
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2013 |
Chen M, Buchwald SL. Continuous-flow synthesis of 1-substituted benzotriazoles from chloronitrobenzenes and amines in a C-N bond formation/hydrogenation/diazotization/cyclization sequence. Angewandte Chemie (International Ed. in English). 52: 4247-50. PMID 23450692 DOI: 10.1002/Anie.201300615 |
0.516 |
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2013 |
Vinogradova EV, Park NH, Fors BP, Buchwald SL. Palladium-catalyzed synthesis of N-aryl carbamates. Organic Letters. 15: 1394-7. PMID 23441814 DOI: 10.1021/Ol400369N |
0.797 |
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2013 |
DeAngelis A, Wang DH, Buchwald SL. Mild and rapid Pd-catalyzed cross-coupling with hydrazine in continuous flow: application to the synthesis of functionalized heterocycles. Angewandte Chemie (International Ed. in English). 52: 3434-7. PMID 23404773 DOI: 10.1002/Anie.201208544 |
0.822 |
|
2013 |
Wang X, Buchwald SL. Synthesis of optically pure 2-trifluoromethyl lactic acid by asymmetric hydroformylation. The Journal of Organic Chemistry. 78: 3429-33. PMID 23394066 DOI: 10.1021/Jo400115R |
0.405 |
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2013 |
Yang Y, Oldenhuis NJ, Buchwald SL. Mild and general conditions for negishi cross-coupling enabled by the use of palladacycle precatalysts. Angewandte Chemie (International Ed. in English). 52: 615-9. PMID 23172689 DOI: 10.1002/Anie.201207750 |
0.487 |
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2012 |
Spokoyny AM, Lewis CD, Teverovskiy G, Buchwald SL. Extremely Electron-Rich, Boron-Functionalized, Icosahedral Carborane-Based Phosphinoboranes. Organometallics. 31: 8478-8481. PMID 23667288 DOI: 10.1021/Om301116X |
0.798 |
|
2012 |
Hoshiya N, Buchwald SL. An Improved Synthesis of BrettPhos and RockPhos-Type Biarylphosphine Ligands. Advanced Synthesis & Catalysis. 354: 2031-2037. PMID 23539491 DOI: 10.1002/Adsc.201200398 |
0.391 |
|
2012 |
Milner PJ, Maimone TJ, Su M, Chen J, Müller P, Buchwald SL. Investigating the dearomative rearrangement of biaryl phosphine-ligated Pd(II) complexes. Journal of the American Chemical Society. 134: 19922-34. PMID 23153301 DOI: 10.1021/Ja310351E |
0.804 |
|
2012 |
Tsvelikhovsky D, Buchwald SL. Correction to Synthesis of Heterocycles via Pd-Ligand Controlled Cyclization of 2-Chloro-N-(2-vinyl)aniline: Preparation of Carbazoles, Indoles, Dibenzazepines, and Acridines. Journal of the American Chemical Society. 134: 16917. PMID 23009568 DOI: 10.1021/ja3066094 |
0.324 |
|
2012 |
Ueda S, Buchwald SL. Catalyst-controlled chemoselective arylation of 2-aminobenzimidazoles. Angewandte Chemie (International Ed. in English). 51: 10364-7. PMID 22969040 DOI: 10.1002/Anie.201204710 |
0.462 |
|
2012 |
Oberli MA, Buchwald SL. A general method for Suzuki-Miyaura coupling reactions using lithium triisopropyl borates. Organic Letters. 14: 4606-9. PMID 22894743 DOI: 10.1021/Ol302063G |
0.44 |
|
2012 |
Cheung CW, Buchwald SL. Room temperature copper(II)-catalyzed oxidative cyclization of enamides to 2,5-disubstituted oxazoles via vinylic C-H functionalization. The Journal of Organic Chemistry. 77: 7526-37. PMID 22838632 DOI: 10.1021/Jo301332S |
0.438 |
|
2012 |
Chernyak N, Buchwald SL. Continuous-flow synthesis of monoarylated acetaldehydes using aryldiazonium salts. Journal of the American Chemical Society. 134: 12466-9. PMID 22812501 DOI: 10.1021/Ja305660A |
0.68 |
|
2012 |
Zhu R, Buchwald SL. Copper-catalyzed oxytrifluoromethylation of unactivated alkenes. Journal of the American Chemical Society. 134: 12462-5. PMID 22804336 DOI: 10.1021/Ja305840G |
0.536 |
|
2012 |
McGowan MA, McAvoy CZ, Buchwald SL. Palladium-catalyzed N-monoarylation of amidines and a one-pot synthesis of quinazoline derivatives. Organic Letters. 14: 3800-3. PMID 22765354 DOI: 10.1021/Ol301700Y |
0.855 |
|
2012 |
Vinogradova EV, Fors BP, Buchwald SL. Palladium-catalyzed cross-coupling of aryl chlorides and triflates with sodium cyanate: a practical synthesis of unsymmetrical ureas. Journal of the American Chemical Society. 134: 11132-5. PMID 22716197 DOI: 10.1021/Ja305212V |
0.781 |
|
2012 |
Shu W, Buchwald SL. Enantioselective β-arylation of ketones enabled by lithiation/borylation/1,4-addition sequence under flow conditions. Angewandte Chemie (International Ed. in English). 51: 5355-8. PMID 22511537 DOI: 10.1002/Anie.201202221 |
0.32 |
|
2012 |
Su M, Buchwald SL. A bulky biaryl phosphine ligand allows for palladium-catalyzed amidation of five-membered heterocycles as electrophiles. Angewandte Chemie (International Ed. in English). 51: 4710-3. PMID 22473747 DOI: 10.1002/Anie.201201244 |
0.685 |
|
2012 |
McGowan MA, Henderson JL, Buchwald SL. Palladium-catalyzed N-arylation of 2-aminothiazoles. Organic Letters. 14: 1432-5. PMID 22394197 DOI: 10.1021/Ol300178J |
0.51 |
|
2012 |
Parsons AT, Senecal TD, Buchwald SL. Iron(II)-catalyzed trifluoromethylation of potassium vinyltrifluoroborates. Angewandte Chemie (International Ed. in English). 51: 2947-50. PMID 22328162 DOI: 10.1002/Anie.201108267 |
0.813 |
|
2012 |
Ueda S, Ali S, Fors BP, Buchwald SL. Me3(OMe)tBuXPhos: a surrogate ligand for Me4tBuXPhos in palladium-catalyzed C-N and C-O bond-forming reactions. The Journal of Organic Chemistry. 77: 2543-7. PMID 22313416 DOI: 10.1021/Jo202537E |
0.691 |
|
2012 |
Zhu R, Buchwald SL. Combined oxypalladation/C-H functionalization: palladium(II)-catalyzed intramolecular oxidative oxyarylation of hydroxyalkenes. Angewandte Chemie (International Ed. in English). 51: 1926-9. PMID 22237989 DOI: 10.1002/Anie.201108129 |
0.576 |
|
2012 |
Salvi L, Davis NR, Ali SZ, Buchwald SL. A new biarylphosphine ligand for the Pd-catalyzed synthesis of diaryl ethers under mild conditions. Organic Letters. 14: 170-3. PMID 22182186 DOI: 10.1021/Ol202955H |
0.701 |
|
2012 |
Ueda S, Su M, Buchwald SL. Completely N1-selective palladium-catalyzed arylation of unsymmetric imidazoles: application to the synthesis of nilotinib. Journal of the American Chemical Society. 134: 700-6. PMID 22126442 DOI: 10.1021/Ja2102373 |
0.625 |
|
2012 |
Chernyak N, Buchwald SL. Correction to Continuous-Flow Synthesis of Monoarylated Acetaldehydes Using Aryldiazonium Salts Journal of the American Chemical Society. 134: 18147-18147. DOI: 10.1021/Ja309119Y |
0.591 |
|
2011 |
Surry DS, Buchwald SL. Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide. Chemical Science. 2: 27-50. PMID 22432049 DOI: 10.1039/C0Sc00331J |
0.447 |
|
2011 |
Maiti D, Fors BP, Henderson JL, Nakamura Y, Buchwald SL. Palladium-Catalyzed Coupling of Functionalized Primary and Secondary Amines with Aryl and Heteroaryl Halides: Two Ligands Suffice in Most Cases. Chemical Science. 2: 57-68. PMID 22384311 DOI: 10.1039/C0Sc00330A |
0.793 |
|
2011 |
Parsons AT, Buchwald SL. Organic chemistry: A radical approach to diversity. Nature. 480: 184-5. PMID 22158236 DOI: 10.1038/480184A |
0.677 |
|
2011 |
Cho EJ, Buchwald SL. The palladium-catalyzed trifluoromethylation of vinyl sulfonates. Organic Letters. 13: 6552-5. PMID 22111687 DOI: 10.1021/Ol202885W |
0.64 |
|
2011 |
Wang X, Buchwald SL. Rh-catalyzed asymmetric hydroformylation of functionalized 1,1-disubstituted olefins. Journal of the American Chemical Society. 133: 19080-3. PMID 22035143 DOI: 10.1021/Ja2092689 |
0.482 |
|
2011 |
Maimone TJ, Milner PJ, Kinzel T, Zhang Y, Takase MK, Buchwald SL. Evidence for in situ catalyst modification during the Pd-catalyzed conversion of aryl triflates to aryl fluorides. Journal of the American Chemical Society. 133: 18106-9. PMID 21999801 DOI: 10.1021/Ja208461K |
0.808 |
|
2011 |
Shu W, Pellegatti L, Oberli MA, Buchwald SL. Continuous-flow synthesis of biaryls enabled by multistep solid-handling in a lithiation/borylation/Suzuki-Miyaura cross-coupling sequence. Angewandte Chemie (International Ed. in English). 50: 10665-9. PMID 21932237 DOI: 10.1002/Anie.201105223 |
0.342 |
|
2011 |
Parsons AT, Buchwald SL. Copper-catalyzed trifluoromethylation of unactivated olefins. Angewandte Chemie (International Ed. in English). 50: 9120-3. PMID 21919144 DOI: 10.1002/Anie.201104053 |
0.687 |
|
2011 |
Wu X, Fors BP, Buchwald SL. A single phosphine ligand allows palladium-catalyzed intermolecular C-O bond formation with secondary and primary alcohols. Angewandte Chemie (International Ed. in English). 50: 9943-7. PMID 21913292 DOI: 10.1002/Anie.201104361 |
0.682 |
|
2011 |
Pan J, Wang X, Zhang Y, Buchwald SL. An improved palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides. Organic Letters. 13: 4974-6. PMID 21863838 DOI: 10.1021/Ol202098H |
0.54 |
|
2011 |
Ueda S, Su M, Buchwald SL. Highly N2-selective palladium-catalyzed arylation of 1,2,3-triazoles. Angewandte Chemie (International Ed. in English). 50: 8944-7. PMID 21853510 DOI: 10.1002/Anie.201103882 |
0.624 |
|
2011 |
Tsvelikhovsky D, Buchwald SL. Concise palladium-catalyzed synthesis of dibenzodiazepines and structural analogues. Journal of the American Chemical Society. 133: 14228-31. PMID 21838278 DOI: 10.1021/Ja206229Y |
0.461 |
|
2011 |
Noël T, Maimone TJ, Buchwald SL. Accelerating palladium-catalyzed C-F bond formation: use of a microflow packed-bed reactor. Angewandte Chemie (International Ed. in English). 50: 8900-3. PMID 21837710 DOI: 10.1002/Anie.201104652 |
0.774 |
|
2011 |
Noël T, Buchwald SL. Cross-coupling in flow. Chemical Society Reviews. 40: 5010-29. PMID 21826351 DOI: 10.1039/C1Cs15075H |
0.559 |
|
2011 |
Pan J, Su M, Buchwald SL. Palladium(0)-catalyzed intermolecular amination of unactivated C(sp³)-H bonds. Angewandte Chemie (International Ed. in English). 50: 8647-51. PMID 21812078 DOI: 10.1002/Anie.201102880 |
0.546 |
|
2011 |
Teverovskiy G, Surry DS, Buchwald SL. Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions. Angewandte Chemie (International Ed. in English). 50: 7312-4. PMID 21692157 DOI: 10.1002/Ange.201102543 |
0.814 |
|
2011 |
Li P, Buchwald SL. Continuous-flow synthesis of 3,3-disubstituted oxindoles by a palladium-catalyzed α-arylation/alkylation sequence. Angewandte Chemie (International Ed. in English). 50: 6396-400. PMID 21656623 DOI: 10.1002/Anie.201102401 |
0.403 |
|
2011 |
Rousseaux S, García-Fortanet J, Del Aguila Sanchez MA, Buchwald SL. Palladium(0)-catalyzed arylative dearomatization of phenols. Journal of the American Chemical Society. 133: 9282-5. PMID 21612204 DOI: 10.1021/Ja203644Q |
0.481 |
|
2011 |
Breitler S, Oldenhuis NJ, Fors BP, Buchwald SL. Synthesis of unsymmetrical diarylureas via Pd-catalyzed C-N cross-coupling reactions. Organic Letters. 13: 3262-5. PMID 21604792 DOI: 10.1021/Ol201210T |
0.728 |
|
2011 |
Noël T, Kuhn S, Musacchio AJ, Jensen KF, Buchwald SL. Suzuki-Miyaura cross-coupling reactions in flow: multistep synthesis enabled by a microfluidic extraction. Angewandte Chemie (International Ed. in English). 50: 5943-6. PMID 21591040 DOI: 10.1002/Anie.201101480 |
0.591 |
|
2011 |
Senecal TD, Parsons AT, Buchwald SL. Room temperature aryl trifluoromethylation via copper-mediated oxidative cross-coupling. The Journal of Organic Chemistry. 76: 1174-6. PMID 21235259 DOI: 10.1021/Jo1023377 |
0.821 |
|
2011 |
Tsvelikhovsky D, Buchwald SL. Concise Palladium-Catalyzed Synthesis of Dibenzodiazepines Synfacts. 2011: 1163-1163. DOI: 10.1055/S-0031-1289284 |
0.515 |
|
2011 |
Teverovskiy G, Surry DS, Buchwald SL. Pd-Catalyzed Synthesis of (Het)Ar-SCF3 Compounds Synfacts. 2011: 1119-1119. DOI: 10.1055/S-0030-1261079 |
0.81 |
|
2011 |
Buchwald S, Fors B. A Multiligand-Based Palladium Catalyst for C-N Cross-Coupling Reactions Synfacts. 2011: 0199-0199. DOI: 10.1055/S-0030-1259242 |
0.703 |
|
2011 |
Shu W, Buchwald SL. Use of precatalysts greatly facilitate palladium-catalyzed alkynylations in batch and continuous-flow conditions Chemical Science. 2: 2321-2325. DOI: 10.1039/C1Sc00409C |
0.42 |
|
2011 |
Noël T, Naber JR, Hartman RL, Mcmullen JP, Jensen KF, Buchwald SL. Palladium-catalyzed amination reactions in flow: Overcoming the challenges of clogging via acoustic irradiation Chemical Science. 2: 287-290. DOI: 10.1039/C0Sc00524J |
0.827 |
|
2011 |
Noel T, Buchwald SL. ChemInform Abstract: Cross-Coupling in Flow Cheminform. 43: no-no. DOI: 10.1002/chin.201204225 |
0.454 |
|
2010 |
Naber JR, Fors BP, Wu X, Gunn J, Buchwald SL. STILLE CROSS-COUPLING REACTIONS OF ARYL MESYLATES AND TOSYLATES USING A BIARYLPHOSPHINE BASED CATALYST SYSTEM. Heterocycles. 80: 1215-1226. PMID 23596345 DOI: 10.3987/Com-09-S(S)105 |
0.854 |
|
2010 |
Surry DS, Buchwald SL. Diamine Ligands in Copper-Catalyzed Reactions. Chemical Science. 1: 13-31. PMID 22384310 DOI: 10.1039/C0Sc00107D |
0.477 |
|
2010 |
Naber JR, Buchwald SL. Packed-bed reactors for continuous-flow C-N cross-coupling. Angewandte Chemie (International Ed. in English). 49: 9469-74. PMID 21038337 DOI: 10.1002/Anie.201004425 |
0.749 |
|
2010 |
Fors BP, Buchwald SL. A multiligand based Pd catalyst for C-N cross-coupling reactions. Journal of the American Chemical Society. 132: 15914-7. PMID 20979367 DOI: 10.1021/Ja108074T |
0.72 |
|
2010 |
Henderson JL, Buchwald SL. Efficient Pd-catalyzed amination reactions for heterocycle functionalization. Organic Letters. 12: 4442-5. PMID 20860403 DOI: 10.1021/Ol101929V |
0.458 |
|
2010 |
Henderson JL, McDermott SM, Buchwald SL. Palladium-catalyzed amination of unprotected halo-7-azaindoles. Organic Letters. 12: 4438-41. PMID 20860393 DOI: 10.1055/S-0030-1259416 |
0.523 |
|
2010 |
Tsvelikhovsky D, Buchwald SL. Synthesis of heterocycles via Pd-ligand controlled cyclization of 2-chloro-N-(2-vinyl)aniline: preparation of carbazoles, indoles, dibenzazepines, and acridines. Journal of the American Chemical Society. 132: 14048-51. PMID 20858012 DOI: 10.1021/Ja107511G |
0.461 |
|
2010 |
Kinzel T, Zhang Y, Buchwald SL. A new palladium precatalyst allows for the fast Suzuki-Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic acids. Journal of the American Chemical Society. 132: 14073-5. PMID 20858009 DOI: 10.1021/Ja1073799 |
0.458 |
|
2010 |
Shen X, Hyde AM, Buchwald SL. Palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides. Journal of the American Chemical Society. 132: 14076-8. PMID 20857936 DOI: 10.1021/Ja107481A |
0.82 |
|
2010 |
Shen X, Jones GO, Watson DA, Bhayana B, Buchwald SL. Enantioselective synthesis of axially chiral biaryls by the Pd-catalyzed Suzuki-Miyaura reaction: substrate scope and quantum mechanical investigations. Journal of the American Chemical Society. 132: 11278-87. PMID 20698695 DOI: 10.1021/Ja104297G |
0.798 |
|
2010 |
Maimone TJ, Buchwald SL. Pd-catalyzed O-arylation of ethyl acetohydroximate: synthesis of O-arylhydroxylamines and substituted benzofurans. Journal of the American Chemical Society. 132: 9990-1. PMID 20604520 DOI: 10.1021/Ja1044874 |
0.706 |
|
2010 |
Cho EJ, Senecal TD, Kinzel T, Zhang Y, Watson DA, Buchwald SL. The palladium-catalyzed trifluoromethylation of aryl chlorides. Science (New York, N.Y.). 328: 1679-81. PMID 20576888 DOI: 10.1126/Science.1190524 |
0.839 |
|
2010 |
Dooleweerdt K, Fors BP, Buchwald SL. Pd-catalyzed cross-coupling reactions of amides and aryl mesylates. Organic Letters. 12: 2350-3. PMID 20420379 DOI: 10.1021/Ol100720X |
0.745 |
|
2010 |
Jones GO, Liu P, Houk KN, Buchwald SL. Computational explorations of mechanisms and ligand-directed selectivities of copper-catalyzed Ullmann-type reactions. Journal of the American Chemical Society. 132: 6205-13. PMID 20387898 DOI: 10.1021/Ja100739H |
0.742 |
|
2010 |
Maiti D, Buchwald SL. Cu-catalyzed arylation of phenols: synthesis of sterically hindered and heteroaryl diaryl ethers. The Journal of Organic Chemistry. 75: 1791-4. PMID 20141182 DOI: 10.1021/Jo9026935 |
0.599 |
|
2010 |
Hartman RL, Naber JR, Buchwald SL, Jensen KF. Multistep microchemical synthesis enabled by microfluidic distillation. Angewandte Chemie (International Ed. in English). 49: 899-903. PMID 20025004 DOI: 10.1002/Anie.200904634 |
0.783 |
|
2010 |
Shen X, Buchwald SL. Rhodium-catalyzed asymmetric intramolecular hydroamination of unactivated alkenes. Angewandte Chemie (International Ed. in English). 49: 564-7. PMID 20014268 DOI: 10.1002/Anie.200905402 |
0.521 |
|
2010 |
Buchwald S, Maimone T. O-Arylhydroxylamines and Benzofurans via O-Arylation of Ethyl Acetohydroximate Synfacts. 2010: 1284-1284. DOI: 10.1055/s-0030-1258705 |
0.574 |
|
2010 |
Watson DA, Su M, Teverovskiy G, Zhang Y, García-Fortanet J, Kinzel T, Buchwald SL. Palladium-Catalyzed Conversion of Aryl Triflates to ArylFluorides Synfacts. 2010: 85-85. DOI: 10.1055/S-0029-1218434 |
0.863 |
|
2010 |
Hartman RL, Naber JR, Zaborenko N, Buchwald SL, Jensen KF. Overcoming the challenges of solid bridging and constriction during Pd-catalyzed C-N bond formation in microreactors Organic Process Research and Development. 14: 1347-1357. DOI: 10.1021/Op100154D |
0.796 |
|
2010 |
Hamada T, Buchwald SL. ChemInform Abstract: P-Chirogenic Binaphthyl-Substituted Monophosphines: Synthesis and Use in Enolate Vinylation/Arylation Reactions. Cheminform. 33: no-no. DOI: 10.1002/chin.200236026 |
0.373 |
|
2010 |
Sturla SJ, Buchwald SL. ChemInform Abstract: Monocyclopentadienyltitanium Aryloxide Complexes: Preparation, Characterization, and Application in Cyclization Reactions. Cheminform. 33: no-no. DOI: 10.1002/chin.200229058 |
0.591 |
|
2010 |
Zhang X, Harris MC, Sadighi JP, Buchwald SL. ChemInform Abstract: The Use of Palladium Chloride as a Precatalyst for the Amination of Aryl Bromides. Cheminform. 33: no-no. DOI: 10.1002/chin.200227065 |
0.802 |
|
2010 |
Moradi WA, Buchwald SL. ChemInform Abstract: Palladium-Catalyzed α-Arylation of Esters. Cheminform. 32: no-no. DOI: 10.1002/chin.200151107 |
0.306 |
|
2010 |
Moritani Y, Appella DH, Jurkauskas V, Buchwald SL. ChemInform Abstract: Synthesis of β-Alkyl Cyclopentanones in High Enantiomeric Excess via Copper-Catalyzed Asymmetric Conjugate Reduction. Cheminform. 31: no-no. DOI: 10.1002/chin.200046030 |
0.827 |
|
2010 |
Fox JM, Huang X, Chieffi A, Buchwald SL. ChemInform Abstract: Highly Active and Selective Catalysts for the Formation of α-Aryl Ketones. Cheminform. 31: no-no. DOI: 10.1002/chin.200021064 |
0.56 |
|
2010 |
Buchwald SL, Hicks FA. ChemInform Abstract: Pauson-Khand-Type Reactions Cheminform. 31: no-no. DOI: 10.1002/chin.200018244 |
0.72 |
|
2010 |
Wagaw S, Yang BH, Buchwald SL. ChemInform Abstract: A Palladium-Catalyzed Method for the Preparation of Indoles via the Fischer Indole Synthesis. Cheminform. 31: no-no. DOI: 10.1002/chin.200012126 |
0.393 |
|
2010 |
Wolfe JP, Singer RA, Yang BH, Buchwald SL. ChemInform Abstract: Highly Active Palladium Catalysts for Suzuki Coupling Reactions. Cheminform. 31: no-no. DOI: 10.1002/chin.200006062 |
0.619 |
|
2010 |
Appella DH, Moritani Y, Shintani R, Ferreira EM, Buchwald SL. ChemInform Abstract: Asymmetric Conjugate Reduction of α,β-Unsaturated Esters Using a Chiral Phosphine-Copper Catalyst. Cheminform. 31: no-no. DOI: 10.1002/chin.200004030 |
0.737 |
|
2010 |
Hicks FA, Buchwald SL. ChemInform Abstract: An Intramolecular Titanium-Catalyzed Asymmetric Pauson-Khand Type Reaction. Cheminform. 30: no-no. DOI: 10.1002/chin.199951028 |
0.757 |
|
2010 |
Yun J, Buchwald SL. ChemInform Abstract: Titanocene-Catalyzed Asymmetric Ketone Hydrosilylation: The Effect of Catalyst Activation Protocol and Additives on the Reaction Rate and Enantioselectivity. Cheminform. 30: no-no. DOI: 10.1002/chin.199942027 |
0.581 |
|
2010 |
Hicks FA, Kablaoui NM, Buchwald SL. ChemInform Abstract: Scope of the Intramolecular Titanocene-Catalyzed Pauson-Khand Type Reaction. Cheminform. 30: no-no. DOI: 10.1002/chin.199941033 |
0.832 |
|
2010 |
Aranyos A, Old DW, Kiyomori A, Wolfe JP, Sadighi JP, Buchwald SL. ChemInform Abstract: Novel Electron-Rich Bulky Phosphine Ligands Facilitate the Palladium-Catalyzed Preparation of Diaryl Ethers. Cheminform. 30: no-no. DOI: 10.1002/chin.199936105 |
0.766 |
|
2010 |
Troutman MV, Appella DH, Buchwald SL. ChemInform Abstract: Asymmetric Hydrogenation of Unfunctionalized Tetrasubstituted Olefins with a Cationic Zirconocene Catalyst. Cheminform. 30: no-no. DOI: 10.1002/chin.199936066 |
0.618 |
|
2010 |
Yang BH, Buchwald SL. ChemInform Abstract: Palladium-Catalyzed Amination of Aryl Halides and Sulfonates Cheminform. 30: no-no. DOI: 10.1002/chin.199931326 |
0.472 |
|
2010 |
Sturla SJ, Kablaoui NM, Buchwald SL. ChemInform Abstract: A Titanocene-Catalyzed Intramolecular Ene Reaction: Cycloisomerization of Enynes and Dienynes. Cheminform. 30: no-no. DOI: 10.1002/chin.199929044 |
0.82 |
|
2010 |
Kiyomori A, Marcoux J, Buchwald SL. ChemInform Abstract: An Efficient Copper-Catalyzed Coupling of Aryl Halides with Imidazoles. Cheminform. 30: no-no. DOI: 10.1002/chin.199927145 |
0.343 |
|
2010 |
Singer RA, Buchwald SL. ChemInform Abstract: Preparation of 2-Amino-2′-hydroxy-1,1′-binaphthyl and N-Arylated 2-Amino-1,1′-binaphthyl Derivatives via Palladium-Catalyzed Amination. Cheminform. 30: no-no. DOI: 10.1002/chin.199921103 |
0.317 |
|
2010 |
Wolfe JP, Wagaw S, Marcoux J, Buchwald SL. ChemInform Abstract: Rational Development of Practical Catalysts for Aromatic Carbon-Nitrogen Bond Formation Cheminform. 30: no-no. DOI: 10.1002/chin.199912328 |
0.526 |
|
2010 |
OLD DW, WOLFE JP, BUCHWALD SL. ChemInform Abstract: A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides. Cheminform. 30: no-no. DOI: 10.1002/chin.199905063 |
0.628 |
|
2010 |
WAGAW S, YANG BH, BUCHWALD SL. ChemInform Abstract: A Palladium-Catalyzed Strategy for the Preparation of Indoles: A Novel Entry into the Fischer Indole Synthesis. Cheminform. 29: no-no. DOI: 10.1002/chin.199846131 |
0.388 |
|
2010 |
SADIGHI JP, HARRIS MC, BUCHWALD SL. ChemInform Abstract: A Highly Active Palladium Catalyst System for the Arylation of Anilines. Cheminform. 29: no-no. DOI: 10.1002/chin.199841080 |
0.782 |
|
2010 |
SADIGHI JP, SINGER RA, BUCHWALD SL. ChemInform Abstract: Palladium-Catalyzed Synthesis of Monodisperse, Controlled-Length, and Functionalized Oligoanilines. Cheminform. 29: no-no. DOI: 10.1002/chin.199837092 |
0.699 |
|
2010 |
HANSEN MC, VERDAGUER X, BUCHWALD SL. ChemInform Abstract: Convenient Two-Step Conversion of Lactones into Cyclic Ethers. Cheminform. 29: no-no. DOI: 10.1002/chin.199831097 |
0.311 |
|
2010 |
VERDAGUER X, LANGE UEW, BUCHWALD SL. ChemInform Abstract: Amine Additives Greatly Expand the Scope of Asymmetric Hydrosilylation of Imines. Cheminform. 29: no-no. DOI: 10.1002/chin.199831035 |
0.378 |
|
2010 |
AAHMAN J, WOLFE JP, TROUTMAN MV, PALUCKI M, BUCHWALD SL. ChemInform Abstract: Asymmetric Arylation of Ketone Enolates. Cheminform. 29: no-no. DOI: 10.1002/chin.199825052 |
0.638 |
|
2010 |
SINGER RA, SADIGHI JP, BUCHWALD SL. ChemInform Abstract: A General Synthesis of End-Functionalized Oligoanilines via Palladium-Catalyzed Amination. Cheminform. 29: no-no. DOI: 10.1002/chin.199817086 |
0.729 |
|
2010 |
PALUCKI M, BUCHWALD SL. ChemInform Abstract: Palladium-Catalyzed α-Arylation of Ketones. Cheminform. 29: no-no. DOI: 10.1002/chin.199809087 |
0.317 |
|
2010 |
MARCOUX J, DOYE S, BUCHWALD SL. ChemInform Abstract: A General Copper-Catalyzed Synthesis of Diaryl Ethers. Cheminform. 29: no-no. DOI: 10.1002/chin.199807122 |
0.636 |
|
2010 |
WOLFE JP, BUCHWALD SL. ChemInform Abstract: Room Temperature Catalytic Amination of Aryl Iodides. Cheminform. 29: no-no. DOI: 10.1002/chin.199803057 |
0.549 |
|
2010 |
WOLFE JP, AAHMAN J, SADIGHI JP, SINGER RA, BUCHWALD SL. ChemInform Abstract: An Ammonia Equivalent for the Palladium-Catalyzed Amination of Aryl Halides and Triflates. Cheminform. 28: no-no. DOI: 10.1002/chin.199749102 |
0.817 |
|
2010 |
WOLFE JP, BUCHWALD SL. ChemInform Abstract: Improved Functional Group Compatibility in the Palladium-Catalyzed Amination of Aryl Bromides. Cheminform. 28: no-no. DOI: 10.1002/chin.199749100 |
0.596 |
|
2010 |
WOLFE JP, BUCHWALD SL. ChemInform Abstract: Nickel-Catalyzed Amination of Aryl Chlorides. Cheminform. 28: no-no. DOI: 10.1002/chin.199742064 |
0.651 |
|
2010 |
KABLAOUI NM, HICKS FA, BUCHWALD SL. ChemInform Abstract: Titanocene-Catalyzed Cyclocarbonylation of o-Allyl Aryl Ketones to . gamma.-Butyrolactones. Cheminform. 28: no-no. DOI: 10.1002/chin.199736122 |
0.813 |
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2010 |
MARCOUX J, WAGAW S, BUCHWALD SL. ChemInform Abstract: Palladium-Catalyzed Amination of Aryl Bromides: Use of Phosphinoether Ligands for the Efficient Coupling of Acyclic Secondary Amines. Cheminform. 28: no-no. DOI: 10.1002/chin.199733098 |
0.39 |
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2010 |
PALUCKI M, WOLFE JP, BUCHWALD SL. ChemInform Abstract: Palladium-Catalyzed Intermolecular Carbon-Oxygen Bond Formation: A New Synthesis of Aryl Ethers. Cheminform. 28: no-no. DOI: 10.1002/chin.199732017 |
0.56 |
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2010 |
GURAM AS, RENNELS RA, BUCHWALD SL, BARTA NS, PEARSON WH. ChemInform Abstract: Palladium-Catalyzed Amination of Aryl Halides with Amines Cheminform. 28: no-no. DOI: 10.1002/chin.199714314 |
0.473 |
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2010 |
HICKS FA, BUCHWALD SL. ChemInform Abstract: Highly Enantioselective Catalytic Pauson-Khand Type Formation of Bicyclic Cyclopentenones. Cheminform. 28: no-no. DOI: 10.1002/chin.199711041 |
0.736 |
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2010 |
PALUCKI M, WOLFE JP, BUCHWALD SL. ChemInform Abstract: Synthesis of Oxygen Heterocycles via a Palladium-Catalyzed C-O Bond- Forming Reaction. Cheminform. 28: no-no. DOI: 10.1002/chin.199707150 |
0.576 |
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2010 |
HICKS FA, KABLAOUI NM, BUCHWALD SL. ChemInform Abstract: Titanocene-Catalyzed Cyclocarbonylation of Enynes to Cyclopentenones. Cheminform. 28: no-no. DOI: 10.1002/chin.199703130 |
0.839 |
|
2010 |
CHIN B, BUCHWALD SL. ChemInform Abstract: An Improved Procedure for the Resolution of (rac)-Ethylenebis( tetrahydroindenyl)titanium Derivatives. Cheminform. 28: no-no. DOI: 10.1002/chin.199702152 |
0.499 |
|
2010 |
WOLFE JP, WAGAW S, BUCHWALD SL. ChemInform Abstract: Improved Catalyst System for Aromatic Carbon-Nitrogen Bond Formation: The Possible Involvement of Bis(Phosphine) Palladium Complexes as Key Intermediates. Cheminform. 27: no-no. DOI: 10.1002/chin.199645086 |
0.577 |
|
2010 |
VERDAGUER X, LANGE UEW, REDING MT, BUCHWALD SL. ChemInform Abstract: Highly Enantioselective Imine Hydrosilylation Using (S,S)-Ethylenebis(. eta.5-tetrahydroindenyl)titanium Difluoride. Cheminform. 27: no-no. DOI: 10.1002/chin.199644069 |
0.66 |
|
2010 |
KABLAOUI NM, HICKS FA, BUCHWALD SL. ChemInform Abstract: Diastereoselective Synthesis of γ-Butyrolactones from Enones Mediated or Catalyzed by a Titanocene Complex. Cheminform. 27: no-no. DOI: 10.1002/chin.199639139 |
0.833 |
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2010 |
WOLFE JP, RENNELS RA, BUCHWALD SL. ChemInform Abstract: Intramolecular Palladium-Catalyzed Aryl Amination and Aryl Amidation. Cheminform. 27: no-no. DOI: 10.1002/chin.199638071 |
0.672 |
|
2010 |
KABLAOUI NM, BUCHWALD SL. ChemInform Abstract: Development of a Method for the Reductive Cyclization of Enones by a Titanium Catalyst. Cheminform. 27: no-no. DOI: 10.1002/chin.199630070 |
0.752 |
|
2010 |
WOLFE JP, BUCHWALD SL. ChemInform Abstract: Palladium-Catalyzed Amination of Aryl Iodides. Cheminform. 27: no-no. DOI: 10.1002/chin.199627112 |
0.674 |
|
2010 |
VERDAGUER X, BERK SC, BUCHWALD SL. ChemInform Abstract: Catalytic Method for the Reduction of Lactones to Lactols. Cheminform. 27: no-no. DOI: 10.1002/chin.199616072 |
0.705 |
|
2010 |
REDING MT, BUCHWALD SL. ChemInform Abstract: An Inexpensive Air-Stable Titanium-Based System for the Conversion of Esters to Primary Alcohols. Cheminform. 27: no-no. DOI: 10.1002/chin.199615070 |
0.65 |
|
2010 |
JOHNSON JR, CUNY GD, BUCHWALD SL. ChemInform Abstract: Rhodium-Catalyzed Hydroformylation of Internal Alkynes to α,. beta.-Unsaturated Aldehydes. Cheminform. 26: no-no. DOI: 10.1002/chin.199548084 |
0.542 |
|
2010 |
KABLAOUI NM, BUCHWALD SL. ChemInform Abstract: Reductive Cyclization of Enones by a Titanium Catalyst. Cheminform. 26: no-no. DOI: 10.1002/chin.199543069 |
0.752 |
|
2010 |
CUNY GD, BUCHWALD SL. ChemInform Abstract: Regioselective Olefin Hydroformylation as a Route to Indolizidine and Pyrrolizidine Alkaloids. Cheminform. 26: no-no. DOI: 10.1002/chin.199540237 |
0.592 |
|
2010 |
GURAM AS, RENNELS RA, BUCHWALD SL. ChemInform Abstract: A Simple Catalytic Method for the Conversion of Aryl Bromides to Arylamines. Cheminform. 26: no-no. DOI: 10.1002/chin.199540100 |
0.352 |
|
2010 |
DE REGE FMG, BUCHWALD SL. ChemInform Abstract: The Regioselective Synthesis of Halophenols. Cheminform. 26: no-no. DOI: 10.1002/chin.199535113 |
0.316 |
|
2010 |
TIDWELL JH, PEAT AJ, BUCHWALD SL. ChemInform Abstract: Synthesis and Reactions of 3-(Bromomethyl)-1-carbethoxy-4-iodoindole: The Preparation of 3,4-Differentially Substituted Indoles. Cheminform. 26: no-no. DOI: 10.1002/chin.199523116 |
0.672 |
|
2010 |
TIDWELL JH, BUCHWALD SL. ChemInform Abstract: Synthesis of Polysubstituted Indoles and Indolines by Means of Zirconocene-Stabilized Benzyne Complexes. Cheminform. 26: no-no. DOI: 10.1002/chin.199522123 |
0.604 |
|
2010 |
CARTER MB, SCHIOTT B, GUTIERREZ A, BUCHWALD SL. ChemInform Abstract: Enantioselective Hydrosilylation of Ketones with a Chiral Titanocene Catalyst. Cheminform. 26: no-no. DOI: 10.1002/chin.199521039 |
0.611 |
|
2010 |
HSU DP, WARNER BP, FISHER RA, DAVIS WM, BUCHWALD SL. ChemInform Abstract: Synthesis and Structure of a Novel Bis(stibole). Cheminform. 26: no-no. DOI: 10.1002/chin.199520162 |
0.685 |
|
2010 |
GURAM AS, BUCHWALD SL. ChemInform Abstract: Palladium-Catalyzed Aromatic Aminations with in situ Generated Aminostannanes. Cheminform. 26: no-no. DOI: 10.1002/chin.199515092 |
0.41 |
|
2010 |
WARNER BP, BUCHWALD SL. ChemInform Abstract: A Catalytic Method for the Conversion of Silanes to Stannanes. Cheminform. 26: no-no. DOI: 10.1002/chin.199514202 |
0.689 |
|
2010 |
BARR KJ, BERK SC, BUCHWALD SL. ChemInform Abstract: Titanocene-Catalyzed Reduction of Esters Using Polymethylhydrosiloxane as the Stoichiometric Reductant. Cheminform. 26: no-no. DOI: 10.1002/chin.199505085 |
0.815 |
|
2010 |
WILLOUGHBY CA, BUCHWALD SL. ChemInform Abstract: Synthesis of Highly Enantiomerically Enriched Cyclic Amines by the Catalytic Asymmetric Hydrogenation of Cyclic Imines. Cheminform. 25: no-no. DOI: 10.1002/chin.199419041 |
0.346 |
|
2010 |
BROENE RD, BUCHWALD SL. ChemInform Abstract: Asymmetric Hydrogenation of Unfunctionalized Trisubstituted Olefins with a Chiral Titanocene Catalyst. Cheminform. 25: no-no. DOI: 10.1002/chin.199415056 |
0.772 |
|
2010 |
BERK SC, GROSSMAN RB, BUCHWALD SL. ChemInform Abstract: Titanocene-Catalyzed Conversion of Enynes to Bicyclic Cyclopentenones. Cheminform. 24: no-no. DOI: 10.1002/chin.199340158 |
0.812 |
|
2010 |
CUNY GD, BUCHWALD SL. ChemInform Abstract: Practical, High-Yield, Regioselective, Rhodium-Catalyzed Hydroformylation of Functionalized α-Olefins. Cheminform. 24: no-no. DOI: 10.1002/chin.199330120 |
0.588 |
|
2010 |
GROSSMAN RB, BUCHWALD SL. ChemInform Abstract: Reductive Cyclization of Ester-Containing Enynes with a Practical Titanocene Reagent. Synthesis of Bicyclic Cyclopentenones and Iminocyclopentenes. Cheminform. 24: no-no. DOI: 10.1002/chin.199309065 |
0.609 |
|
2010 |
BARR KJ, WATSON BT, BUCHWALD SL. ChemInform Abstract: Zirconocene(iso-butyl) Chloride: In situ Generation of a Zirconocene( methyl) Chloride Equivalent for Use in Organic Synthesis. Cheminform. 23: no-no. DOI: 10.1002/chin.199225234 |
0.782 |
|
2010 |
BERK SC, KREUTZER KA, BUCHWALD SL. ChemInform Abstract: A Catalytic Method for the Reduction of Esters to Alcohols. Cheminform. 22: no-no. DOI: 10.1002/chin.199141081 |
0.674 |
|
2010 |
HSU DP, LUCAS EA, BUCHWALD SL. ChemInform Abstract: Synthesis and Reactions of a Zirconocene-Benzdiyne Equivalent. Cheminform. 22: no-no. DOI: 10.1002/chin.199140201 |
0.618 |
|
2010 |
GROSSMAN RB, DAVIS WM, BUCHWALD SL. ChemInform Abstract: Enantioselective, Zirconium-Mediated Synthesis of Allylic Amines. Cheminform. 22: no-no. DOI: 10.1002/chin.199130134 |
0.646 |
|
2010 |
CUNY GD, GUTIERREZ A, BUCHWALD SL. ChemInform Abstract: Cis Difunctionalization of Cyclic Olefins with Use of Organozirconium Intermediates. Cheminform. 22: no-no. DOI: 10.1002/chin.199129138 |
0.508 |
|
2010 |
CUNY GD, BUCHWALD SL. ChemInform Abstract: Ring-Opening Reactions of Cyclic Allylic Ethers by Zirconocene Complexes of Cyclic Alkynes. Cheminform. 22: no-no. DOI: 10.1002/chin.199117054 |
0.628 |
|
2010 |
BUCHWALD SL, KING SM. ChemInform Abstract: Regiospecific Synthesis of Polysubstituted Naphthalenes and Iodoacylnaphthoquinones via Zirconocene Complexes of Naphthalynes. Cheminform. 22: no-no. DOI: 10.1002/chin.199115141 |
0.688 |
|
2010 |
Fors BP, Buchwald SL. Commentary on "a new, efficient and recyclable lanthanum(III) oxide-catalyzed C-N cross-coupling" by S. Narayana Murthy, B. Madhav, V. Prakash Reddy, and Y. V. D. Nageswar, Adv. Synth. Catal. 2010, 352, 3241-3245 Advanced Synthesis and Catalysis. 352: 3119-3120. DOI: 10.1002/Adsc.201000905 |
0.62 |
|
2009 |
Lee BK, Biscoe MR, Buchwald SL. Simple, Efficient Protocols for the Pd-Catalyzed Cross-Coupling Reaction of Aryl Chlorides and Dimethylamine. Tetrahedron Letters. 50: 3672-3674. PMID 21818164 DOI: 10.1016/J.Tetlet.2009.03.137 |
0.778 |
|
2009 |
Fors BP, Dooleweerdt K, Zeng Q, Buchwald SL. An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides. Tetrahedron. 65: 6576-6583. PMID 20740063 DOI: 10.1016/J.Tet.2009.04.096 |
0.752 |
|
2009 |
Maiti D, Buchwald SL. Orthogonal Cu- and Pd-based catalyst systems for the O- and N-arylation of aminophenols. Journal of the American Chemical Society. 131: 17423-9. PMID 19899753 DOI: 10.1021/Ja9081815 |
0.59 |
|
2009 |
Hicks JD, Hyde AM, Cuezva AM, Buchwald SL. Pd-catalyzed N-arylation of secondary acyclic amides: catalyst development, scope, and computational study. Journal of the American Chemical Society. 131: 16720-34. PMID 19886610 DOI: 10.1021/Ja9044357 |
0.775 |
|
2009 |
Fors BP, Buchwald SL. Pd-catalyzed conversion of aryl chlorides, triflates, and nonaflates to nitroaromatics. Journal of the American Chemical Society. 131: 12898-9. PMID 19737014 DOI: 10.1021/Ja905768K |
0.739 |
|
2009 |
Watson DA, Su M, Teverovskiy G, Zhang Y, García-Fortanet J, Kinzel T, Buchwald SL. Formation of ArF from LPdAr(F): catalytic conversion of aryl triflates to aryl fluorides. Science (New York, N.Y.). 325: 1661-4. PMID 19679769 DOI: 10.1126/Science.1178239 |
0.828 |
|
2009 |
Bhayana B, Fors BP, Buchwald SL. A versatile catalyst system for Suzuki-Miyaura cross-coupling reactions of C(sp(2))-tosylates and mesylates. Organic Letters. 11: 3954-7. PMID 19663467 DOI: 10.1021/Ol9015892 |
0.734 |
|
2009 |
Taylor AM, Altman RA, Buchwald SL. Palladium-catalyzed enantioselective alpha-arylation and alpha-vinylation of oxindoles facilitated by an axially chiral P-stereogenic ligand. Journal of the American Chemical Society. 131: 9900-1. PMID 19580273 DOI: 10.1021/Ja903880Q |
0.69 |
|
2009 |
Buchwald SL, Bolm C. On the role of metal contaminants in catalyses with FeCl3. Angewandte Chemie (International Ed. in English). 48: 5586-7. PMID 19554587 DOI: 10.1002/Anie.200902237 |
0.447 |
|
2009 |
Hyde AM, Buchwald SL. Synthesis of 5,5-disubstituted butenolides based on a Pd-catalyzed gamma-arylation strategy. Organic Letters. 11: 2663-6. PMID 19449882 DOI: 10.1021/Ol9007102 |
0.779 |
|
2009 |
Han C, Buchwald SL. Negishi coupling of secondary alkylzinc halides with aryl bromides and chlorides. Journal of the American Chemical Society. 131: 7532-3. PMID 19441851 DOI: 10.1021/Ja902046M |
0.634 |
|
2009 |
García-Fortanet J, Kessler F, Buchwald SL. Palladium-catalyzed asymmetric dearomatization of naphthalene derivatives. Journal of the American Chemical Society. 131: 6676-7. PMID 19388652 DOI: 10.1021/Ja9025193 |
0.525 |
|
2009 |
Fors BP, Davis NR, Buchwald SL. An efficient process for pd-catalyzed C-N cross-coupling reactions of aryl iodides: insight into controlling factors. Journal of the American Chemical Society. 131: 5766-8. PMID 19348431 DOI: 10.1021/Ja901414U |
0.823 |
|
2009 |
Biscoe MR, Buchwald SL. Selective monoarylation of acetate esters and aryl methyl ketones using aryl chlorides. Organic Letters. 11: 1773-5. PMID 19296693 DOI: 10.1021/Ol900295U |
0.787 |
|
2009 |
Strieter ER, Bhayana B, Buchwald SL. Mechanistic studies on the copper-catalyzed N-arylation of amides. Journal of the American Chemical Society. 131: 78-88. PMID 19072233 DOI: 10.1021/Ja0781893 |
0.768 |
|
2009 |
Buchwald S, Fors B. Palladium-Catalyzed Synthesis of Nitroarenes Using Sodium Nitrite Synfacts. 2009: 1388-1388. DOI: 10.1055/S-0029-1218172 |
0.731 |
|
2009 |
Buchwald S, Bhayana B, Fors B. A Versatile Ligand for Suzuki-Miyaura Coupling of Tosylates and Mesylates Synfacts. 2009: 1385-1385. DOI: 10.1055/S-0029-1218165 |
0.651 |
|
2009 |
Taylor AM, Altman RA, Buchwald SL. Pd-Catalyzed Asymmetric α-Arylation and α-Vinylationof Oxindoles Synfacts. 2009: 1116-1116. DOI: 10.1055/S-0029-1217838 |
0.355 |
|
2009 |
García-Fortanet J, Kessler F, Buchwald SL. Palladium-Catalyzed Asymmetric Dearomatization Synfacts. 2009: 887-887. DOI: 10.1055/S-0029-1217423 |
0.556 |
|
2009 |
Garcia-Fortanet J, Buchwald SL. ChemInform Abstract: Asymmetric Palladium-Catalyzed Intramolecular α-Arylation of Aldehydes. Cheminform. 40. DOI: 10.1002/CHIN.200907100 |
0.351 |
|
2008 |
Martín R, Buchwald SL. An improved protocol for the Pd-catalyzed alpha-arylation of aldehydes with aryl halides. Organic Letters. 10: 4561-4. PMID 18808127 DOI: 10.1021/Ol8017775 |
0.772 |
|
2008 |
Fors BP, Watson DA, Biscoe MR, Buchwald SL. A highly active catalyst for Pd-catalyzed amination reactions: cross-coupling reactions using aryl mesylates and the highly selective monoarylation of primary amines using aryl chlorides. Journal of the American Chemical Society. 130: 13552-4. PMID 18798626 DOI: 10.1021/Ja8055358 |
0.858 |
|
2008 |
García-Fortanet J, Buchwald SL. Asymmetric palladium-catalyzed intramolecular alpha-arylation of aldehydes. Angewandte Chemie (International Ed. in English). 47: 8108-11. PMID 18792905 DOI: 10.1002/Anie.200803809 |
0.512 |
|
2008 |
Tsang WC, Munday RH, Brasche G, Zheng N, Buchwald SL. Palladium-catalyzed method for the synthesis of carbazoles via tandem C-H functionalization and C-N bond formation. The Journal of Organic Chemistry. 73: 7603-10. PMID 18761437 DOI: 10.1021/Jo801273Q |
0.516 |
|
2008 |
Watson DA, Fan X, Buchwald SL. Carbonylation of aryl chlorides with oxygen nucleophiles at atmospheric pressure. Preparation of phenyl esters as acyl transfer agents and the direct preparation of alkyl esters and carboxylic acids. The Journal of Organic Chemistry. 73: 7096-101. PMID 18720992 DOI: 10.1021/Jo800907E |
0.656 |
|
2008 |
Martinelli JR, Watson DA, Freckmann DM, Barder TE, Buchwald SL. Palladium-catalyzed carbonylation reactions of aryl bromides at atmospheric pressure: a general system based on Xantphos. The Journal of Organic Chemistry. 73: 7102-7. PMID 18720970 DOI: 10.1021/Jo801279R |
0.844 |
|
2008 |
Surry DS, Buchwald SL. Biaryl phosphane ligands in palladium-catalyzed amination. Angewandte Chemie (International Ed. in English). 47: 6338-61. PMID 18663711 DOI: 10.1002/Anie.200800497 |
0.537 |
|
2008 |
Martin R, Buchwald SL. Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands. Accounts of Chemical Research. 41: 1461-73. PMID 18620434 DOI: 10.1021/Ar800036S |
0.779 |
|
2008 |
Fors BP, Krattiger P, Strieter E, Buchwald SL. Water-mediated catalyst preactivation: an efficient protocol for C-N cross-coupling reactions. Organic Letters. 10: 3505-8. PMID 18620415 DOI: 10.1021/Ol801285G |
0.828 |
|
2008 |
Altman RA, Hyde AM, Huang X, Buchwald SL. Orthogonal Pd- and Cu-based catalyst systems for C- and N-arylation of oxindoles. Journal of the American Chemical Society. 130: 9613-20. PMID 18588302 DOI: 10.1021/Ja803179S |
0.826 |
|
2008 |
Billingsley KL, Buchwald SL. An improved system for the palladium-catalyzed borylation of aryl halides with pinacol borane. The Journal of Organic Chemistry. 73: 5589-91. PMID 18576604 DOI: 10.1021/Jo800727S |
0.809 |
|
2008 |
Altman RA, Anderson KW, Buchwald SL. Pyrrole-2-carboxylic acid as a ligand for the Cu-catalyzed reactions of primary anilines with aryl halides. The Journal of Organic Chemistry. 73: 5167-9. PMID 18543973 DOI: 10.1021/Jo8008676 |
0.772 |
|
2008 |
Minatti A, Buchwald SL. Synthesis of indolines via a domino Cu-catalyzed amidation/cyclization reaction. Organic Letters. 10: 2721-4. PMID 18522394 DOI: 10.1021/Ol8008792 |
0.491 |
|
2008 |
Billingsley KL, Buchwald SL. A general and efficient method for the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles. Angewandte Chemie (International Ed. in English). 47: 4695-8. PMID 18491343 DOI: 10.1002/Anie.200801465 |
0.822 |
|
2008 |
Wang H, Duennwald ML, Roberts BE, Rozeboom LM, Zhang YL, Steele AD, Krishnan R, Su LJ, Griffin D, Mukhopadhyay S, Hennessy EJ, Weigele P, Blanchard BJ, King J, Deniz AA, ... Buchwald SL, et al. Direct and selective elimination of specific prions and amyloids by 4,5-dianilinophthalimide and analogs. Proceedings of the National Academy of Sciences of the United States of America. 105: 7159-64. PMID 18480256 DOI: 10.1073/Pnas.0801934105 |
0.645 |
|
2008 |
Brasche G, García-Fortanet J, Buchwald SL. Twofold C-H functionalization: palladium-catalyzed ortho arylation of anilides. Organic Letters. 10: 2207-10. PMID 18465866 DOI: 10.1021/Ol800619C |
0.388 |
|
2008 |
Biscoe MR, Fors BP, Buchwald SL. A new class of easily activated palladium precatalysts for facile C-N cross-coupling reactions and the low temperature oxidative addition of aryl chlorides. Journal of the American Chemical Society. 130: 6686-7. PMID 18447360 DOI: 10.1021/Ja801137K |
0.837 |
|
2008 |
Munday RH, Martinelli JR, Buchwald SL. Palladium-catalyzed carbonylation of aryl tosylates and mesylates. Journal of the American Chemical Society. 130: 2754-5. PMID 18257577 DOI: 10.1021/Ja711449E |
0.748 |
|
2008 |
Brasche G, Buchwald SL. C-H functionalization/C-N bond formation: copper-catalyzed synthesis of benzimidazoles from amidines. Angewandte Chemie (International Ed. in English). 47: 1932-4. PMID 18228236 DOI: 10.1002/Anie.200705420 |
0.353 |
|
2008 |
Altman RA, Shafir A, Choi A, Lichtor PA, Buchwald SL. An improved Cu-based catalyst system for the reactions of alcohols with aryl halides. The Journal of Organic Chemistry. 73: 284-6. PMID 18044928 DOI: 10.1021/Jo702024P |
0.727 |
|
2008 |
Hyde AM, Buchwald SL. Palladium-catalyzed gamma-arylation of beta,gamma-unsaturated ketones: application to a one-pot synthesis of tricyclic indolines. Angewandte Chemie (International Ed. in English). 47: 177-80. PMID 18033712 DOI: 10.1002/Anie.200704529 |
0.749 |
|
2008 |
Altman RA, Hyde AM, Huang X, Buchwald SL. N- and C-Arylations of Oxindoles: Orthogonal Selectivityof Pd and Cu Catalysts Synfacts. 2008: 1096-1096. DOI: 10.1055/S-2008-1078230 |
0.394 |
|
2008 |
Munday RH, Martinelli JR, Buchwald SL. Carbonylation of Aryl Tosylates and Mesylates Synfacts. 2008: 515-515. DOI: 10.1055/S-2008-1072526 |
0.754 |
|
2008 |
Martín R, Cuenca A, Buchwald SL. Copper-Catalyzed C-N Bond Coupling Approach to Highly Substituted Oxazoles Synfacts. 2008: 237-237. DOI: 10.1055/S-2008-1042746 |
0.387 |
|
2008 |
Altman RA, Shafir A, Choi A, Lichtor PA, Buchwald SL. An Improved Catalyst System for Ullmann-Type Couplings between Alcohols and Aryl Halides Synfacts. 2008: 303-303. DOI: 10.1055/S-2008-1042741 |
0.374 |
|
2008 |
Martinelli JR, Watson DA, Freckmann DMM, Barder TE, Buchwald SL. Pd-Catalyzed Carbonylation of Aryl Bromides at AtmosphericPressure Synfacts. 2008: 1312-1312. DOI: 10.1055/S-0028-1083588 |
0.816 |
|
2008 |
Buchwald S, Fors B, Krattiger P, Strieter E. Water-Mediated Catalyst Preactivation for Efficient Pd-Catalyzed Aminations Synfacts. 2008: 1206-1206. DOI: 10.1055/S-0028-1083461 |
0.805 |
|
2008 |
Hyde AM, Buchwald SL. ChemInform Abstract: Palladium-Catalyzed γ-Arylation of β,γ-Unsaturated Ketones: Application to a One-Pot Synthesis of Tricyclic Indolines. Cheminform. 39. DOI: 10.1002/chin.200817118 |
0.752 |
|
2008 |
Naber JR, Buchwald SL. Palladium-catalyzed Stille cross-coupling reaction of aryl chlorides using a pre-milled palladium acetate and XPhos catalyst system Advanced Synthesis and Catalysis. 350: 957-961. DOI: 10.1002/Adsc.200800032 |
0.841 |
|
2007 |
Altman RA, Buchwald SL. Pd-catalyzed Suzuki-Miyaura reactions of aryl halides using bulky biarylmonophosphine ligands. Nature Protocols. 2: 3115-21. PMID 18079711 DOI: 10.1038/Nprot.2007.411 |
0.757 |
|
2007 |
Martín R, Cuenca A, Buchwald SL. Sequential copper-catalyzed vinylation/cyclization: an efficient synthesis of functionalized oxazoles. Organic Letters. 9: 5521-4. PMID 18020351 DOI: 10.1021/Ol7024718 |
0.772 |
|
2007 |
Altman RA, Fors BP, Buchwald SL. Pd-catalyzed amination reactions of aryl halides using bulky biarylmonophosphine ligands. Nature Protocols. 2: 2881-7. PMID 18007623 DOI: 10.1038/Nprot.2007.414 |
0.831 |
|
2007 |
Minatti A, Zheng X, Buchwald SL. Synthesis of chiral 3-substituted indanones via an enantioselective reductive-Heck reaction. The Journal of Organic Chemistry. 72: 9253-8. PMID 17967034 DOI: 10.1021/Jo701741Y |
0.518 |
|
2007 |
Zheng N, Buchwald SL. Copper-catalyzed regiospecific synthesis of N-alkylbenzimidazoles. Organic Letters. 9: 4749-51. PMID 17949007 DOI: 10.1021/Ol7020737 |
0.505 |
|
2007 |
Altman RA, Buchwald SL. Cu-catalyzed Goldberg and Ullmann reactions of aryl halides using chelating N- and O-based ligands. Nature Protocols. 2: 2474-9. PMID 17947989 DOI: 10.1038/Nprot.2007.364 |
0.741 |
|
2007 |
Ikawa T, Barder TE, Biscoe MR, Buchwald SL. Pd-catalyzed amidation of aryl chlorides using monodentate biaryl phosphine ligands: a kinetic, computational, and synthetic investigation. Journal of the American Chemical Society. 129: 13001-7. PMID 17918833 DOI: 10.1021/Ja0717414 |
0.85 |
|
2007 |
Martinelli JR, Clark TP, Watson DA, Munday RH, Buchwald SL. Palladium-catalyzed aminocarbonylation of aryl chlorides at atmospheric pressure: the dual role of sodium phenoxide. Angewandte Chemie (International Ed. in English). 46: 8460-3. PMID 17902084 DOI: 10.1002/Anie.200702943 |
0.752 |
|
2007 |
Jones CP, Anderson KW, Buchwald SL. Sequential Cu-catalyzed amidation-base-mediated camps cyclization: a two-step synthesis of 2-Aryl-4-quinolones from o-halophenones. The Journal of Organic Chemistry. 72: 7968-73. PMID 17850097 DOI: 10.1021/Jo701384N |
0.788 |
|
2007 |
Barder TE, Buchwald SL. Insights into amine binding to biaryl phosphine palladium oxidative addition complexes and reductive elimination from biaryl phosphine arylpalladium amido complexes via density functional theory. Journal of the American Chemical Society. 129: 12003-10. PMID 17850080 DOI: 10.1021/Ja073747Z |
0.769 |
|
2007 |
Martín R, Buchwald SL. A general method for the direct alpha-arylation of aldehydes with aryl bromides and chlorides. Angewandte Chemie (International Ed. in English). 46: 7236-9. PMID 17722128 DOI: 10.1002/Anie.200703009 |
0.723 |
|
2007 |
Zheng N, Anderson KW, Huang X, Nguyen HN, Buchwald SL. A palladium-catalyzed regiospecific synthesis of N-aryl benzimidazoles. Angewandte Chemie (International Ed. in English). 46: 7509-12. PMID 17722125 DOI: 10.1002/Anie.200702542 |
0.766 |
|
2007 |
McNeill E, Barder TE, Buchwald SL. Palladium-catalyzed silylation of aryl chlorides with hexamethyldisilane. Organic Letters. 9: 3785-8. PMID 17705501 DOI: 10.1021/Ol701518F |
0.815 |
|
2007 |
Biscoe MR, Barder TE, Buchwald SL. Electronic effects on the selectivity of pd-catalyzed C-N bond-forming reactions using biarylphosphine ligands: the competitive roles of amine binding and acidity. Angewandte Chemie (International Ed. in English). 46: 7232-5. PMID 17680583 DOI: 10.1002/Anie.200702122 |
0.823 |
|
2007 |
Surry DS, Buchwald SL. Selective palladium-catalyzed arylation of ammonia: synthesis of anilines as well as symmetrical and unsymmetrical di- and triarylamines. Journal of the American Chemical Society. 129: 10354-5. PMID 17672469 DOI: 10.1021/Ja074681A |
0.506 |
|
2007 |
Martín R, Larsen CH, Cuenca A, Buchwald SL. Cu-catalyzed tandem C-N bond formation for the synthesis of pyrroles and heteroarylpyrroles. Organic Letters. 9: 3379-82. PMID 17655316 DOI: 10.1021/Ol7014225 |
0.827 |
|
2007 |
Altman RA, Koval ED, Buchwald SL. Copper-catalyzed N-arylation of imidazoles and benzimidazoles. The Journal of Organic Chemistry. 72: 6190-9. PMID 17625886 DOI: 10.1021/Jo070807A |
0.754 |
|
2007 |
Billingsley KL, Barder TE, Buchwald SL. Palladium-catalyzed borylation of aryl chlorides: scope, applications, and computational studies. Angewandte Chemie (International Ed. in English). 46: 5359-63. PMID 17562550 DOI: 10.1002/Anie.200701551 |
0.818 |
|
2007 |
Murphy ER, Martinelli JR, Zaborenko N, Buchwald SL, Jensen KF. Accelerating reactions with microreactors at elevated temperatures and pressures: profiling aminocarbonylation reactions. Angewandte Chemie (International Ed. in English). 46: 1734-7. PMID 17397088 DOI: 10.1002/Anie.200604175 |
0.663 |
|
2007 |
Barder TE, Buchwald SL. Rationale behind the resistance of dialkylbiaryl phosphines toward oxidation by molecular oxygen. Journal of the American Chemical Society. 129: 5096-101. PMID 17388595 DOI: 10.1021/Ja0683180 |
0.763 |
|
2007 |
Martin R, Buchwald SL. Pd-catalyzed Kumada-Corriu cross-coupling reactions at low temperatures allow the use of Knochel-type Grignard reagents. Journal of the American Chemical Society. 129: 3844-5. PMID 17352483 DOI: 10.1021/Ja070830D |
0.778 |
|
2007 |
Shafir A, Lichtor PA, Buchwald SL. N- versus O-arylation of aminoalcohols: orthogonal selectivity in copper-based catalysts. Journal of the American Chemical Society. 129: 3490-1. PMID 17341083 DOI: 10.1021/Ja068926F |
0.447 |
|
2007 |
Billingsley K, Buchwald SL. Highly efficient monophosphine-based catalyst for the palladium-catalyzed suzuki-miyaura reaction of heteroaryl halides and heteroaryl boronic acids and esters. Journal of the American Chemical Society. 129: 3358-66. PMID 17326639 DOI: 10.1021/Ja068577P |
0.811 |
|
2007 |
Rivero MR, Buchwald SL. Copper-catalyzed vinylation of hydrazides. A regioselective entry to highly substituted pyrroles. Organic Letters. 9: 973-6. PMID 17311390 DOI: 10.1021/Ol062978S |
0.503 |
|
2007 |
Altman RA, Buchwald SL. Cu-catalyzed N- and O-arylation of 2-, 3-, and 4-hydroxypyridines and hydroxyquinolines. Organic Letters. 9: 643-6. PMID 17286371 DOI: 10.1021/Ol062904G |
0.718 |
|
2007 |
Barder TE, Buchwald SL. Benchtop monitoring of reaction progress via visual recognition with a handheld UV lamp: in situ monitoring of boronic acids in the Suzuki-Miyaura reaction. Organic Letters. 9: 137-9. PMID 17192104 DOI: 10.1021/Ol062802Q |
0.765 |
|
2007 |
Billingsley KL, Barder TE, Buchwald SL. Palladium-Catalyzed Borylation and Homocoupling of Aryl Chlorides Synfacts. 2007: 1194-1194. DOI: 10.1055/S-2007-991238 |
0.863 |
|
2007 |
Barder TE, Biscoe MR, Buchwald SL. Structural insights into active catalyst structures and oxidative addition to (biaryl)phosphine - palladium complexes via density functional theory and experimental studies Organometallics. 26: 2183-2192. DOI: 10.1021/Om0701017 |
0.823 |
|
2006 |
Martinelli JR, Freckmann DM, Buchwald SL. Convenient method for the preparation of Weinreb amides via Pd-catalyzed aminocarbonylation of aryl bromides at atmospheric pressure. Organic Letters. 8: 4843-6. PMID 17020317 DOI: 10.1021/Ol061902T |
0.703 |
|
2006 |
Martín R, Rodríguez Rivero M, Buchwald SL. Domino cu-catalyzed C--N coupling/hydroamidation: a highly efficient synthesis of nitrogen heterocycles. Angewandte Chemie (International Ed. in English). 45: 7079-82. PMID 17009380 DOI: 10.1002/Anie.200602917 |
0.744 |
|
2006 |
Anderson KW, Tundel RE, Ikawa T, Altman RA, Buchwald SL. Monodentate phosphines provide highly active catalysts for Pd-catalyzed C-N bond-forming reactions of heteroaromatic halides/amines and (H)N-heterocycles. Angewandte Chemie (International Ed. in English). 45: 6523-7. PMID 16955526 DOI: 10.1002/Anie.200601612 |
0.835 |
|
2006 |
Anderson KW, Ikawa T, Tundel RE, Buchwald SL. The selective reaction of aryl halides with KOH: synthesis of phenols, aromatic ethers, and benzofurans. Journal of the American Chemical Society. 128: 10694-5. PMID 16910660 DOI: 10.1021/Ja0639719 |
0.859 |
|
2006 |
Shafir A, Buchwald SL. Highly selective room-temperature copper-catalyzed C-N coupling reactions. Journal of the American Chemical Society. 128: 8742-3. PMID 16819863 DOI: 10.1021/Ja063063B |
0.484 |
|
2006 |
Altman RA, Buchwald SL. 4,7-Dimethoxy-1,10-phenanthroline: an excellent ligand for the Cu-catalyzed N-arylation of imidazoles. Organic Letters. 8: 2779-82. PMID 16774255 DOI: 10.1021/Ol0608505 |
0.737 |
|
2006 |
Burgos CH, Barder TE, Huang X, Buchwald SL. Significantly improved method for the pd-catalyzed coupling of phenols with aryl halides: understanding ligand effects. Angewandte Chemie (International Ed. in English). 45: 4321-6. PMID 16733839 DOI: 10.1002/Anie.200601253 |
0.811 |
|
2006 |
Billingsley KL, Anderson KW, Buchwald SL. A highly active catalyst for Suzuki-Miyaura cross-coupling reactions of heteroaryl compounds. Angewandte Chemie (International Ed. in English). 45: 3484-8. PMID 16639772 DOI: 10.1002/Anie.200600493 |
0.815 |
|
2006 |
Shekhar S, Ryberg P, Hartwig JF, Mathew JS, Blackmond DG, Strieter ER, Buchwald SL. Reevaluation of the mechanism of the amination of aryl halides catalyzed by BINAP-ligated palladium complexes. Journal of the American Chemical Society. 128: 3584-91. PMID 16536531 DOI: 10.1021/Ja045533C |
0.768 |
|
2006 |
Tundel RE, Anderson KW, Buchwald SL. Expedited palladium-catalyzed amination of aryl nonaflates through the use of microwave-irradiation and soluble organic amine bases. The Journal of Organic Chemistry. 71: 430-3. PMID 16388678 DOI: 10.1021/Jo052131U |
0.852 |
|
2006 |
Strieter ER, Buchwald SL. Evidence for the formation and structure of palladacycles during Pd-catalyzed C-N bond formation with catalysts derived from bulky monophosphinobiaryl ligands. Angewandte Chemie (International Ed. in English). 45: 925-8. PMID 16381052 DOI: 10.1002/Anie.200502927 |
0.744 |
|
2006 |
Larsen CH, Anderson KW, Tundel RE, Buchwald SL. Palladium-catalyzed Heck alkynylation of benzyl chlorides Synlett. 2941-2946. DOI: 10.1055/S-2006-949625 |
0.842 |
|
2006 |
Buchwald S, Anderson K, Ikawa T, Tundel R. Pd-Catalyzed Synthesis of Phenols and Aromatic Ethers from Aryl Halides Synfacts. 2006: 1163-1163. DOI: 10.1055/S-2006-949484 |
0.831 |
|
2006 |
Buchwald S, Shafir A. A Mild Copper-Catalyzed Amination of Haloarenes Synfacts. 2006: 1055-1055. DOI: 10.1055/s-2006-949307 |
0.304 |
|
2006 |
Klingensmith LM, Strieter ER, Barder TE, Buchwald SL. New insights into xantphos/Pd-catalyzed C-N bond forming reactions: A structural and kinetic study Organometallics. 25: 82-91. DOI: 10.1021/Om050715G |
0.804 |
|
2006 |
Enguehard-Gueiffier C, Thery I, Gueiffier A, Buchwald SL. A General and Efficient Method for the Copper-Catalyzed Cross-Coupling of Amides and Thiophenols with 6-Halogenoimidazo[1,2-a]pyridines. Cheminform. 37. DOI: 10.1016/J.Tet.2006.04.007 |
0.45 |
|
2006 |
Buchwald S, Mauger C, Mignani G, Scholz U. Cover Picture: Industrial-Scale Palladium-Catalyzed Coupling of Aryl Halides and Amines –A Personal Account (Adv. Synth. Catal. 1-2/2006) Advanced Synthesis & Catalysis. 348: 1-1. DOI: 10.1002/Adsc.200690000 |
0.457 |
|
2006 |
Buchwald S, Mauger C, Mignani G, Scholz U. Industrial-Scale Palladium-Catalyzed Coupling of Aryl Halides and Amines –A Personal Account Advanced Synthesis & Catalysis. 348: 23-39. DOI: 10.1002/Adsc.200505158 |
0.423 |
|
2005 |
Tsang WC, Zheng N, Buchwald SL. Combined C-H functionalization/C-N bond formation route to carbazoles. Journal of the American Chemical Society. 127: 14560-1. PMID 16231894 DOI: 10.1021/Ja055353I |
0.5 |
|
2005 |
Rainka MP, Milne JE, Buchwald SL. Dynamic kinetic resolution of alpha,beta-unsaturated lactones through asymmetric copper-catalyzed conjugate reduction: application to the total synthesis of eupomatilone-3. Angewandte Chemie (International Ed. in English). 44: 6177-80. PMID 16130153 DOI: 10.1002/Anie.200501890 |
0.792 |
|
2005 |
Hennessy EJ, Buchwald SL. Synthesis of 4,5-dianilinophthalimide and related analogues for potential treatment of Alzheimer's disease via palladium-catalyzed amination. The Journal of Organic Chemistry. 70: 7371-5. PMID 16122261 DOI: 10.1021/Jo051096O |
0.75 |
|
2005 |
Charles MD, Schultz P, Buchwald SL. Efficient pd-catalyzed amination of heteroaryl halides. Organic Letters. 7: 3965-8. PMID 16119943 DOI: 10.1021/ol0514754 |
0.351 |
|
2005 |
Anderson KW, Buchwald SL. General catalysts for the Suzuki-Miyaura and Sonogashira coupling reactions of aryl chlorides and for the coupling of challenging substrate combinations in water. Angewandte Chemie (International Ed. in English). 44: 6173-7. PMID 16097019 DOI: 10.1002/Anie.200502017 |
0.653 |
|
2005 |
Vorogushin AV, Huang X, Buchwald SL. Use of tunable ligands allows for intermolecular Pd-catalyzed C--O bond formation. Journal of the American Chemical Society. 127: 8146-9. PMID 15926842 DOI: 10.1021/Ja050471R |
0.603 |
|
2005 |
Barder TE, Walker SD, Martinelli JR, Buchwald SL. Catalysts for Suzuki-Miyaura coupling processes: scope and studies of the effect of ligand structure. Journal of the American Chemical Society. 127: 4685-96. PMID 15796535 DOI: 10.1021/Ja042491J |
0.859 |
|
2005 |
Strieter ER, Blackmond DG, Buchwald SL. The role of chelating diamine ligands in the goldberg reaction: a kinetic study on the copper-catalyzed amidation of aryl iodides. Journal of the American Chemical Society. 127: 4120-1. PMID 15783164 DOI: 10.1021/Ja050120C |
0.733 |
|
2005 |
Buchwald S, Rainka M, Milne J. Dynamic Kinetic Resolution in Cu-Catalyzed Conjugate Hydride Addition Synfacts. 2006: 0034-0034. DOI: 10.1055/S-2005-921676 |
0.777 |
|
2005 |
Charles MD, Schultz P, Buchwald SL. Synthesis of Heteroaromatic Amines by C-N Cross-Coupling Synfacts. 2005: 210-210. DOI: 10.1055/S-2005-916068 |
0.377 |
|
2004 |
Chae J, Yun J, Buchwald SL. One-pot sequential Cu-catalyzed reduction and Pd-catalyzed arylation of silyl enol ethers. Organic Letters. 6: 4809-12. PMID 15606072 DOI: 10.1021/Ol048313C |
0.738 |
|
2004 |
Milne JE, Buchwald SL. An extremely active catalyst for the Negishi cross-coupling reaction. Journal of the American Chemical Society. 126: 13028-32. PMID 15469301 DOI: 10.1021/Ja0474493 |
0.495 |
|
2004 |
Antilla JC, Baskin JM, Barder TE, Buchwald SL. Copper-diamine-catalyzed N-arylation of pyrroles, pyrazoles, indazoles, imidazoles, and triazoles. The Journal of Organic Chemistry. 69: 5578-87. PMID 15307726 DOI: 10.1021/Jo049658B |
0.857 |
|
2004 |
Barder TE, Buchwald SL. Efficient catalyst for the Suzuki-Miyaura coupling of potassium aryl trifluoroborates with aryl chlorides. Organic Letters. 6: 2649-52. PMID 15281735 DOI: 10.1021/Ol0491686 |
0.831 |
|
2004 |
Chae J, Buchwald SL. Palladium-catalyzed regioselective hydrodebromination of dibromoindoles: application to the enantioselective synthesis of indolodioxane U86192A. The Journal of Organic Chemistry. 69: 3336-9. PMID 15132539 DOI: 10.1021/Jo035819K |
0.679 |
|
2004 |
Rainka MP, Aye Y, Buchwald SL. Copper-catalyzed asymmetric conjugate reduction as a route to novel beta-azaheterocyclic acid derivatives. Proceedings of the National Academy of Sciences of the United States of America. 101: 5821-3. PMID 15067136 DOI: 10.1073/Pnas.0307764101 |
0.814 |
|
2004 |
Walker SD, Barder TE, Martinelli JR, Buchwald SL. A rationally designed universal catalyst for Suzuki-Miyaura coupling processes. Angewandte Chemie (International Ed. in English). 43: 1871-6. PMID 15054800 DOI: 10.1002/Anie.200353615 |
0.839 |
|
2004 |
Klapars A, Parris S, Anderson KW, Buchwald SL. Synthesis of medium ring nitrogen heterocycles via a tandem copper-catalyzed C-N bond formation-ring-expansion process. Journal of the American Chemical Society. 126: 3529-33. PMID 15025480 DOI: 10.1021/Ja038565T |
0.646 |
|
2004 |
Murata M, Buchwald SL. A General and Efficient Method for the Palladium-Catalyzed Cross-Coupling of Thiols and Secondary Phosphines. Cheminform. 35. DOI: 10.1016/J.Tet.2004.05.044 |
0.516 |
|
2004 |
Hennessy EJ, Buchwald SL. Synthesis of Substituted Oxindoles from α-Chloroacetanilides via Palladium-Catalyzed C—H Functionalization. Cheminform. 35. DOI: 10.1002/chin.200404090 |
0.721 |
|
2004 |
Buchwald S. Transition Metal-Catalyzed Cross-Coupling and the Heck Coupling Processes: Powerful Reactions for Carbon-Carbon and Carbon-Heteroatom Bond Formation Advanced Synthesis & Catalysis. 346: 1524-1524. DOI: 10.1002/Adsc.200404335 |
0.329 |
|
2003 |
Hughes G, Kimura M, Buchwald SL. Catalytic enantioselective conjugate reduction of lactones and lactams. Journal of the American Chemical Society. 125: 11253-8. PMID 16220945 DOI: 10.1021/Ja0351692 |
0.449 |
|
2003 |
Gelman D, Buchwald SL. Efficient palladium-catalyzed coupling of aryl chlorides and tosylates with terminal alkynes: use of a copper cocatalyst inhibits the reaction. Angewandte Chemie (International Ed. in English). 42: 5993-6. PMID 14679552 DOI: 10.1002/Anie.200353015 |
0.734 |
|
2003 |
Anderson KW, Mendez-Perez M, Priego J, Buchwald SL. Palladium-catalyzed amination of aryl nonaflates. The Journal of Organic Chemistry. 68: 9563-73. PMID 14656080 DOI: 10.1021/Jo034962A |
0.718 |
|
2003 |
Strieter ER, Blackmond DG, Buchwald SL. Insights into the origin of high activity and stability of catalysts derived from bulky, electron-rich monophosphinobiaryl ligands in the Pd-catalyzed C-N bond formation. Journal of the American Chemical Society. 125: 13978-80. PMID 14611232 DOI: 10.1021/Ja037932Y |
0.742 |
|
2003 |
Hennessy EJ, Buchwald SL. Synthesis of substituted oxindoles from alpha-chloroacetanilides via palladium-catalyzed C[bond]H functionalization. Journal of the American Chemical Society. 125: 12084-5. PMID 14518981 DOI: 10.1021/Ja037546G |
0.766 |
|
2003 |
Jiang L, Job GE, Klapars A, Buchwald SL. Copper-catalyzed coupling of amides and carbamates with vinyl halides. Organic Letters. 5: 3667-9. PMID 14507200 DOI: 10.1021/Ol035355C |
0.508 |
|
2003 |
Nguyen HN, Huang X, Buchwald SL. The first general palladium catalyst for the Suzuki-Miyaura and carbonyl enolate coupling of aryl arenesulfonates. Journal of the American Chemical Society. 125: 11818-9. PMID 14505394 DOI: 10.1021/Ja036947T |
0.653 |
|
2003 |
Jurkauskas V, Sadighi JP, Buchwald SL. Conjugate reduction of alpha,beta-unsaturated carbonyl compounds catalyzed by a copper carbene complex. Organic Letters. 5: 2417-20. PMID 12841744 DOI: 10.1021/Ol034560P |
0.819 |
|
2003 |
Zim D, Buchwald SL. An air and thermally stable one- component catalyst for the amination of aryl chlorides. Organic Letters. 5: 2413-5. PMID 12841743 DOI: 10.1021/Ol034561H |
0.446 |
|
2003 |
Enguehard C, Allouchi H, Gueiffier A, Buchwald SL. Ipso- or cine-substitutions of 6-haloimidazo[1,2-a]pyridine derivatives with different azoles depending on the reaction conditions. The Journal of Organic Chemistry. 68: 5614-7. PMID 12839453 DOI: 10.1021/Jo034439W |
0.474 |
|
2003 |
Gelman D, Jiang L, Buchwald SL. Copper-catalyzed C-P bond construction via direct coupling of secondary phosphines and phosphites with aryl and vinyl halides. Organic Letters. 5: 2315-8. PMID 12816437 DOI: 10.1021/Ol0346640 |
0.757 |
|
2003 |
Huang X, Anderson KW, Zim D, Jiang L, Klapars A, Buchwald SL. Expanding Pd-catalyzed C-N bond-forming processes: the first amidation of aryl sulfonates, aqueous amination, and complementarity with Cu-catalyzed reactions. Journal of the American Chemical Society. 125: 6653-5. PMID 12769573 DOI: 10.1021/Ja035483W |
0.749 |
|
2003 |
Enguehard C, Allouchi H, Gueiffier A, Buchwald SL. Easy access to novel substituted 6-aminoimidazo[1,2-a]pyridines using palladium- and copper-catalyzed aminations. The Journal of Organic Chemistry. 68: 4367-70. PMID 12762738 DOI: 10.1021/Jo0341463 |
0.467 |
|
2003 |
Nordmann G, Buchwald SL. A domino copper-catalyzed C-O coupling-Claisen rearrangement process. Journal of the American Chemical Society. 125: 4978-9. PMID 12708838 DOI: 10.1021/Ja034809Y |
0.476 |
|
2003 |
Kwong FY, Buchwald SL. Mild and efficient copper-catalyzed amination of aryl bromides with primary alkylamines. Organic Letters. 5: 793-6. PMID 12633073 DOI: 10.1021/Ol0273396 |
0.694 |
|
2003 |
Zanon J, Klapars A, Buchwald SL. Copper-catalyzed domino halide exchange-cyanation of aryl bromides. Journal of the American Chemical Society. 125: 2890-1. PMID 12617652 DOI: 10.1021/Ja0299708 |
0.521 |
|
2003 |
Huang X, Anderson KW, Zim D, Jiang L, Klapars aA, Buchwald SL. Expanding Pd-Catalyzed C−N Bond-Forming Processes: The First Amidation of Aryl Sulfonates, Aqueous Amination, and Complementarity with Cu-Catalyzed Reactions [J. Am. Chem. Soc. 2003, 125, 6653−6655]. Journal of the American Chemical Society. 125: 10767-10767. DOI: 10.1021/Ja033450A |
0.723 |
|
2003 |
Jurkauskas V, Sadighi JP, Buchwald SL. Conjugate Reduction of α,β-Unsaturated Carbonyl Compounds Catalyzed by a Copper Carbene Complex. Cheminform. 34. DOI: 10.1002/chin.200348047 |
0.8 |
|
2003 |
Buchwald SL, LaMaire SJ, Nielsen RB, Watson BT, King SM. Schwartz's Reagent Organic Syntheses. 77-77. DOI: 10.1002/0471264180.Os071.10 |
0.77 |
|
2002 |
Rutherford JL, Rainka MP, Buchwald SL. An annulative approach to highly substituted indoles: unusual effect of phenolic additives on the success of the arylation of ketone enolates. Journal of the American Chemical Society. 124: 15168-9. PMID 12487580 DOI: 10.1021/Ja0288993 |
0.846 |
|
2002 |
Klapars A, Buchwald SL. Copper-catalyzed halogen exchange in aryl halides: an aromatic Finkelstein reaction. Journal of the American Chemical Society. 124: 14844-5. PMID 12475315 DOI: 10.1021/Ja028865V |
0.518 |
|
2002 |
Singh UK, Strieter ER, Blackmond DG, Buchwald SL. Mechanistic insights into the Pd(BINAP)-catalyzed amination of aryl bromides: kinetic studies under synthetically relevant conditions. Journal of the American Chemical Society. 124: 14104-14. PMID 12440909 DOI: 10.1021/Ja026885R |
0.76 |
|
2002 |
Kwong FY, Buchwald SL. A general, efficient, and inexpensive catalyst system for the coupling of aryl iodides and thiols. Organic Letters. 4: 3517-20. PMID 12323058 DOI: 10.1021/Ol0266673 |
0.688 |
|
2002 |
Antilla JC, Klapars A, Buchwald SL. The copper-catalyzed N-arylation of indoles. Journal of the American Chemical Society. 124: 11684-8. PMID 12296734 DOI: 10.1021/Ja027433H |
0.67 |
|
2002 |
Harris MC, Huang X, Buchwald SL. Improved functional group compatibility in the palladium-catalyzed synthesis of aryl amines. Organic Letters. 4: 2885-8. PMID 12182580 DOI: 10.1021/Ol0262688 |
0.753 |
|
2002 |
Klapars A, Huang X, Buchwald SL. A general and efficient copper catalyst for the amidation of aryl halides. Journal of the American Chemical Society. 124: 7421-8. PMID 12071751 DOI: 10.1021/Ja0260465 |
0.633 |
|
2002 |
Yin J, Buchwald SL. Pd-catalyzed intermolecular amidation of aryl halides: the discovery that xantphos can be trans-chelating in a palladium complex. Journal of the American Chemical Society. 124: 6043-8. PMID 12022838 DOI: 10.1021/Ja012610K |
0.467 |
|
2002 |
Sturla SJ, Buchwald SL. Cobalt-phosphite-catalyzed asymmetric Pauson-Khand reaction. The Journal of Organic Chemistry. 67: 3398-403. PMID 12003551 DOI: 10.1021/Jo016038R |
0.695 |
|
2002 |
Spielvogel DJ, Buchwald SL. Nickel-BINAP catalyzed enantioselective alpha-arylation of alpha-substituted gamma-butyrolactones. Journal of the American Chemical Society. 124: 3500-1. PMID 11929227 DOI: 10.1021/Ja017545T |
0.306 |
|
2002 |
Jurkauskas V, Buchwald SL. Dynamic kinetic resolution via asymmetric conjugate reduction: enantio- and diastereoselective synthesis of 2,4-dialkyl cyclopentanones. Journal of the American Chemical Society. 124: 2892-3. PMID 11902878 DOI: 10.1021/Ja025603K |
0.817 |
|
2002 |
Hamada T, Buchwald SL. P-chirogenic binaphthyl-substituted monophosphines: synthesis and use in enolate vinylation/arylation reactions. Organic Letters. 4: 999-1001. PMID 11893206 DOI: 10.1021/Ol025563P |
0.421 |
|
2002 |
Wolter M, Nordmann G, Job GE, Buchwald SL. Copper-catalyzed coupling of aryl iodides with aliphatic alcohols. Organic Letters. 4: 973-6. PMID 11893199 DOI: 10.1021/Ol025548K |
0.344 |
|
2002 |
Kwong FY, Klapars A, Buchwald SL. Copper-catalyzed coupling of alkylamines and aryl iodides: an efficient system even in an air atmosphere. Organic Letters. 4: 581-4. PMID 11843596 DOI: 10.1021/Ol0171867 |
0.714 |
|
2002 |
Hamada T, Chieffi A, Ahman J, Buchwald SL. An improved catalyst for the asymmetric arylation of ketone enolates. Journal of the American Chemical Society. 124: 1261-8. PMID 11841295 DOI: 10.1021/Ja011122+ |
0.784 |
|
2002 |
Yin J, Rainka MP, Zhang XX, Buchwald SL. A highly active Suzuki catalyst for the synthesis of sterically hindered biaryls: novel ligand coordination. Journal of the American Chemical Society. 124: 1162-3. PMID 11841272 DOI: 10.1021/Ja017082R |
0.825 |
|
2002 |
Gaertzen O, Buchwald SL. Palladium-catalyzed intramolecular alpha-arylation of alpha-amino acid esters. The Journal of Organic Chemistry. 67: 465-75. PMID 11798319 DOI: 10.1021/Jo0107756 |
0.377 |
|
2002 |
Hennessy EJ, Buchwald SL. A general and mild copper-catalyzed arylation of diethyl malonate. Organic Letters. 4: 269-72. PMID 11796067 DOI: 10.1021/Ol017038G |
0.775 |
|
2002 |
Vogl EM, Buchwald SL. Palladium-catalyzed monoarylation of nitroalkanes. The Journal of Organic Chemistry. 67: 106-11. PMID 11777446 DOI: 10.1021/Jo010953V |
0.539 |
|
2002 |
Wolfe JP, Buchwald SL, Norling H, Hegedus LS. Palladium-catalyzed amination of aryl halides and aryl triflates: N-hexyl-2-methyl-4-methoxyaniline and N-methyl-N-(4-chlorophenyl) aniline: [ Benzenamine, 4-chloro-N-methyl-N-phenyl- ] Organic Syntheses. 78: 23-35. DOI: 10.15227/Orgsyn.078.0023 |
0.547 |
|
2002 |
Sturla SJ, Buchwald SL. Monocyclopentadienyltitanium aryloxide complexes: Preparation, characterization, and application in cyclization reactions Organometallics. 21: 739-748. DOI: 10.1021/Om010755U |
0.664 |
|
2002 |
Muci AR, Buchwald SL. Practical Palladium Catalysts for C-N and C-O Bond Formation Topics in Current Chemistry. 219: 131-209. DOI: 10.1007/3-540-45313-X_5 |
0.452 |
|
2001 |
Kuwabe SI, Torraca KE, Buchwald SL. Palladium-catalyzed intramolecular C-O bond formation. Journal of the American Chemical Society. 123: 12202-6. PMID 11734019 DOI: 10.1021/Ja012046D |
0.847 |
|
2001 |
Wolter M, Klapars A, Buchwald SL. Synthesis of N-aryl hydrazides by copper-catalyzed coupling of hydrazides with aryl iodides. Organic Letters. 3: 3803-5. PMID 11700143 DOI: 10.1021/Ol0168216 |
0.486 |
|
2001 |
Torraca KE, Huang X, Parrish CA, Buchwald SL. An efficient intermolecular palladium-catalyzed synthesis of aryl ethers. Journal of the American Chemical Society. 123: 10770-1. PMID 11674023 DOI: 10.1021/Ja016863P |
0.853 |
|
2001 |
Huang X, Buchwald SL. New ammonia equivalents for the Pd-catalyzed amination of aryl halides. Organic Letters. 3: 3417-9. PMID 11594848 DOI: 10.1021/Ol0166808 |
0.64 |
|
2001 |
Moradi WA, Buchwald SL. Palladium-catalyzed alpha-arylation of esters. Journal of the American Chemical Society. 123: 7996-8002. PMID 11506555 DOI: 10.1021/Ja010797+ |
0.497 |
|
2001 |
Klapars A, Antilla JC, Huang X, Buchwald SL. A general and efficient copper catalyst for the amidation of aryl halides and the N-arylation of nitrogen heterocycles. Journal of the American Chemical Society. 123: 7727-9. PMID 11481007 DOI: 10.1021/Ja016226Z |
0.768 |
|
2001 |
Antilla JC, Buchwald SL. Copper-catalyzed coupling of arylboronic acids and amines. Organic Letters. 3: 2077-9. PMID 11418053 DOI: 10.1021/Ol0160396 |
0.719 |
|
2001 |
Chieffi A, Kamikawa K, Ahman J, Fox JM, Buchwald SL. Catalytic asymmetric vinylation of ketone enolates. Organic Letters. 3: 1897-900. PMID 11405739 DOI: 10.1021/Ol0159470 |
0.825 |
|
2001 |
Parrish CA, Buchwald SL. Use of polymer-supported dialkylphosphinobiphenyl ligands for palladium-catalyzed amination and Suzuki reactions. The Journal of Organic Chemistry. 66: 3820-7. PMID 11375003 DOI: 10.1021/Jo010025W |
0.492 |
|
2001 |
Yun J, Buchwald SL. One-pot synthesis of enantiomerically enriched 2,3-disubstituted cyclopentanones via copper-catalyzed 1,4-reduction and alkylation. Organic Letters. 3: 1129-31. PMID 11348176 DOI: 10.1021/Ol015577F |
0.665 |
|
2001 |
Ali MH, Buchwald SL. An improved method for the palladium-catalyzed amination of aryl iodides. The Journal of Organic Chemistry. 66: 2560-5. PMID 11304171 DOI: 10.1021/Jo0008486 |
0.534 |
|
2001 |
Parrish CA, Buchwald SL. Palladium-catalyzed formation of aryl tert-butyl ethers from unactivated aryl halides. The Journal of Organic Chemistry. 66: 2498-500. PMID 11281795 DOI: 10.1021/Jo001426Z |
0.546 |
|
2001 |
Zhang X, Harris MC, Sadighi JP, Buchwald SL. The use of palladium chloride as a precatalyst for the amination of aryl bromides Canadian Journal of Chemistry. 79: 1799-1805. DOI: 10.1139/V01-152 |
0.847 |
|
2001 |
Yin J, Buchwald SL. ChemInform Abstract: A Catalytic Asymmetric Suzuki Coupling for the Synthesis of Axially Chiral Biaryl Compounds. Cheminform. 32: no-no. DOI: 10.1002/chin.200116119 |
0.326 |
|
2001 |
Torraca KE, Kuwabe S, Buchwald SL. ChemInform Abstract: A High-Yield, General Method for the Catalytic Formation of Oxygen Heterocycles. Cheminform. 32: no-no. DOI: 10.1002/chin.200116057 |
0.792 |
|
2001 |
Kaye S, Fox JM, Hicks FA, Buchwald SL. The Use of Catalytic Amounts of CuCl and Other Improvements in the Benzyne Route to Biphenyl-Based Phosphine Ligands Advanced Synthesis and Catalysis. 343: 789-794. DOI: 10.1002/1615-4169(20011231)343:8<789::Aid-Adsc789>3.0.Co;2-A |
0.795 |
|
2001 |
Wolfe JP, Buchwald SL. Palladium-catalyzed amination of aryl halides and aryl triflates: N-hexyl-2-methyl-4-methoxyaniline and N-methyl-N-(4-chlorophenyl)aniline Organic Syntheses. 78: 23-30. DOI: 10.1002/0471264180.Os078.03 |
0.572 |
|
2000 |
Zhang XX, Buchwald SL. Efficient synthesis of N-aryl-aza-crown ethers via palladium-catalyzed amination The Journal of Organic Chemistry. 65: 8027-31. PMID 11073613 DOI: 10.1021/Jo005577D |
0.532 |
|
2000 |
Tomori H, Fox JM, Buchwald SL. An improved synthesis of functionalized biphenyl-based phosphine ligands. The Journal of Organic Chemistry. 65: 5334-41. PMID 10993363 DOI: 10.1021/Jo000691H |
0.613 |
|
2000 |
Harris MC, Buchwald SL. One-pot synthesis of unsymmetrical triarylamines from aniline precursors. The Journal of Organic Chemistry. 65: 5327-33. PMID 10993362 DOI: 10.1021/Jo000674S |
0.708 |
|
2000 |
Hundertmark T, Littke AF, Buchwald SL, Fu GC. Pd(PhCN)(2)Cl(2)/P(t-Bu)(3): a versatile catalyst for Sonogashira reactions of aryl bromides at room temperature. Organic Letters. 2: 1729-31. PMID 10880212 DOI: 10.1021/Ol0058947 |
0.621 |
|
2000 |
Yun J, Buchwald SL. Kinetic resolution and isomerization of 2,5-disubstituted pyrrolines. Chirality. 12: 476-8. PMID 10824173 DOI: 10.1002/(Sici)1520-636X(2000)12:5/6<476::Aid-Chir31>3.0.Co;2-B |
0.618 |
|
2000 |
Old DW, Harris MC, Buchwald SL. Efficient palladium-catalyzed N-arylation of indoles. Organic Letters. 2: 1403-6. PMID 10814458 DOI: 10.1021/Ol005728Z |
0.716 |
|
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