| Year |
Citation |
Score |
| 2024 |
Shezaf JZ, Santana CG, Ortiz E, Meyer CC, Liu P, Sakata K, Huang KW, Krische MJ. Leveraging the Stereochemical Complexity of Octahedral Diastereomeric-at-Metal Catalysts to Unlock Regio-, Diastereo-, and Enantioselectivity in Alcohol-Mediated C-C Couplings via Hydrogen Transfer. Journal of the American Chemical Society. 146: 7905-7914. PMID 38478891 DOI: 10.1021/jacs.4c01857 |
0.313 |
|
| 2023 |
Spinello BJ, Strong ZH, Ortiz E, Evarts MM, Krische MJ. Intermolecular Metal-Catalyzed C‒C Coupling of Unactivated Alcohols or Aldehydes for Convergent Ketone Construction beyond Premetalated Reagents. Acs Catalysis. 13: 10976-10987. PMID 38464997 DOI: 10.1021/acscatal.3c02209 |
0.36 |
|
| 2023 |
Saludares C, Ortiz E, Santana CG, Spinello BJ, Krische MJ. Asymmetric Ruthenium-Catalyzed Carbonyl Allylations by Gaseous Allene via Hydrogen Auto-Transfer: 1° vs 2° Alcohol Dehydrogenation for Streamlined Polyketide Construction. Acs Catalysis. 13: 1662-1668. PMID 37869365 DOI: 10.1021/acscatal.2c05425 |
0.36 |
|
| 2023 |
Chang YH, Shen W, Shezaf JZ, Ortiz E, Krische MJ. Palladium(I)-Iodide-Catalyzed Deoxygenative Heck Reaction of Vinyl Triflates: A Formate-Mediated Cross-Electrophile Reductive Coupling with -Substitution. Journal of the American Chemical Society. 145: 22890-22895. PMID 37845783 DOI: 10.1021/jacs.3c09876 |
0.367 |
|
| 2023 |
Ortiz E, Saludares C, Wu J, Cho Y, Santana CG, Krische MJ. Carbonyl Allylation and Crotylation: Historical Perspective, Relevance to Polyketide Synthesis, and Evolution of Enantioselective Ruthenium-Catalyzed Hydrogen Auto-Transfer Processes. Synthesis. 55: 1487-1496. PMID 37841289 DOI: 10.1055/s-0042-1751420 |
0.399 |
|
| 2023 |
Shezaf JZ, Santana CG, Saludares C, Briceno ES, Sakata K, Krische MJ. Chiral-at-Ruthenium-SEGPHOS Catalysts Display Diastereomer-Dependent Regioselectivity: Enantioselective Isoprene-Mediated Carbonyl -Prenylation via Halide Counterion Effects. Journal of the American Chemical Society. 145: 18676-18683. PMID 37555765 DOI: 10.1021/jacs.3c06734 |
0.372 |
|
| 2023 |
Huynh NO, Hodík T, Krische MJ. Enantioselective Transfer Hydrogenative Cycloaddition Unlocks the Total Synthesis of SF2446 B3: An Aglycone of Arenimycin and SF2446 Type II Polyketide Antibiotics. Journal of the American Chemical Society. PMID 37494281 DOI: 10.1021/jacs.3c06225 |
0.351 |
|
| 2023 |
Verboom KL, Meyer CC, Evarts MM, Jung WO, Krische MJ. Acetyl 1,3-Propanediol as an Acrolein Proelectrophile in Enantioselective Iridium-Catalyzed Carbonyl Allylation. Organic Letters. PMID 37172193 DOI: 10.1021/acs.orglett.3c01022 |
0.382 |
|
| 2023 |
Dubey ZJ, Shen W, Little JA, Krische MJ. Dual Ruthenium-Catalyzed Alkene Isomerization-Hydrogen Auto-Transfer Unlocks Skipped Dienes as Pronucleophiles for Enantioselective Alcohol C-H Allylation. Journal of the American Chemical Society. PMID 37018070 DOI: 10.1021/jacs.3c00934 |
0.451 |
|
| 2023 |
Ortiz E, Evarts MM, Strong ZH, Shezaf JZ, Krische MJ. Ruthenium-Catalyzed C-C Coupling of Terminal Alkynes with Primary Alcohols or Aldehydes: α,β-Acetylenic Ketones (Ynones) via Oxidative Alkynylation. Angewandte Chemie (International Ed. in English). e202303345. PMID 37000412 DOI: 10.1002/anie.202303345 |
0.342 |
|
| 2023 |
Meyer CC, Verboom KL, Evarts MM, Jung WO, Krische MJ. Allyl Alcohol as an Acrolein Equivalent in Enantioselective C-C Coupling: Total Synthesis of Amphidinolides R, J, and S. Journal of the American Chemical Society. 145: 8242-8247. PMID 36996284 DOI: 10.1021/jacs.3c01809 |
0.372 |
|
| 2022 |
Ortiz E, Shezaf J, Chang YH, Krische MJ. Enantioselective Metal-Catalyzed Reductive Coupling of Alkynes with Carbonyl Compounds and Imines: Convergent Construction of Allylic Alcohols and Amines. Acs Catalysis. 12: 8164-8174. PMID 37082110 DOI: 10.1021/acscatal.2c02444 |
0.397 |
|
| 2022 |
Stafford NP, Cheng MJ, Dinh DN, Verboom KL, Krische MJ. Chiral α-Stereogenic Oxetanols and Azetidinols Alcohol-Mediated Reductive Coupling of Allylic Acetates: Enantiotopic π-Facial Selection in Symmetric Ketone Addition. Acs Catalysis. 12: 6172-6179. PMID 37063244 DOI: 10.1021/acscatal.2c01647 |
0.429 |
|
| 2022 |
Ortiz E, Shezaf JZ, Shen W, Krische MJ. Historical perspective on ruthenium-catalyzed hydrogen transfer and survey of enantioselective hydrogen auto-transfer processes for the conversion of lower alcohols to higher alcohols. Chemical Science. 13: 12625-12633. PMID 36516346 DOI: 10.1039/d2sc05621f |
0.334 |
|
| 2022 |
Meyer CC, Krische MJ. Iridium-, Ruthenium-, and Nickel-Catalyzed C-C Couplings of Methanol, Formaldehyde, and Ethanol with π-Unsaturated Pronucleophiles via Hydrogen Transfer. The Journal of Organic Chemistry. PMID 36449710 DOI: 10.1021/acs.joc.2c02356 |
0.392 |
|
| 2022 |
Liang X, Yoo M, Schempp T, Maejima S, Krische MJ. Ruthenium-Catalyzed Butadiene-Mediated Crotylation and Oxazaborolidine-Catalyzed Vinylogous Mukaiyama Aldol Reaction for The Synthesis of C1-C19 and C23-C35 of Neaumycin B. Angewandte Chemie (International Ed. in English). e202214786. PMID 36322115 DOI: 10.1002/anie.202214786 |
0.367 |
|
| 2022 |
Ortiz E, Spinello BJ, Cho Y, Wu J, Krische MJ. Stereo- and Site-Selective Crotylation of Alcohol Proelectrophiles via Ruthenium-Catalyzed Hydrogen Auto-Transfer Mediated by Methylallene and Butadiene. Angewandte Chemie (International Ed. in English). PMID 36201364 DOI: 10.1002/anie.202212814 |
0.362 |
|
| 2022 |
Jung WO, Mai BK, Yoo M, Shields SWJ, Zbieg JR, Stivala CE, Liu P, Krische MJ. Kinetic, ESI-CID-MS and Computational Studies of π-Allyliridium -Benzoate-Catalyzed Allylic Amination: Understanding the Effect of Cesium Ion. Acs Catalysis. 12: 3660-3668. PMID 36092640 DOI: 10.1021/acscatal.2c00470 |
0.32 |
|
| 2022 |
Stivala CE, Zbieg JR, Liu P, Krische MJ. Chiral Amines via Enantioselective π-Allyliridium-,-Benzoate-Catalyzed Allylic Alkylation: Student Training via Industrial-Academic Collaboration. Accounts of Chemical Research. PMID 35830564 DOI: 10.1021/acs.accounts.2c00302 |
0.4 |
|
| 2022 |
Ortiz E, Chang YH, Shezaf JZ, Shen W, Krische MJ. Stereo- and Site-Selective Conversion of Primary Alcohols to Allylic Alcohols via Ruthenium-Catalyzed Hydrogen Auto-Transfer Mediated by 2-Butyne. Journal of the American Chemical Society. PMID 35503919 DOI: 10.1021/jacs.2c03614 |
0.408 |
|
| 2022 |
Meyer CC, Dubey ZJ, Krische MJ. Enantioselective Iridium-Catalyzed Reductive Coupling of Dienes with Oxetanones and N-Acyl-Azetidinones Mediated by 2-Propanol. Angewandte Chemie (International Ed. in English). e202115959. PMID 35119714 DOI: 10.1002/anie.202115959 |
0.377 |
|
| 2022 |
Schempp TT, Krische MJ. Total Synthesis of the Acetyl CoA Carboxylase Inhibitor Soraphen A: Asymmetric Tsuji Reduction Enables Successive Olefin Metathesis. Journal of the American Chemical Society. 144: 1016-1022. PMID 35005976 DOI: 10.1021/jacs.1c12063 |
0.396 |
|
| 2022 |
Jung WO, Yoo M, Migliozzi MM, Zbieg JR, Stivala CE, Krische MJ. Regio- and Enantioselective Iridium-Catalyzed Amination of Alkyl-Substituted Allylic Acetates with Secondary Amines. Organic Letters. 24: 441-445. PMID 34905364 DOI: 10.1021/acs.orglett.1c04135 |
0.431 |
|
| 2021 |
Ortiz E, Shezaf JZ, Chang YH, Gonçalves TP, Huang KW, Krische MJ. Understanding Halide Counterion Effects in Enantioselective Ruthenium-Catalyzed Carbonyl (α-Aryl)allylation: Alkynes as Latent Allenes and Trifluoroethanol-Enhanced Turnover in The Conversion of Ethanol to Higher Alcohols via Hydrogen Auto-transfer. Journal of the American Chemical Society. PMID 34606271 DOI: 10.1021/jacs.1c07857 |
0.423 |
|
| 2021 |
Spinello BJ, Wu J, Cho Y, Krische MJ. Conversion of Primary Alcohols and Butadiene to Branched Ketones via Merged Transfer Hydrogenative Carbonyl Addition-Redox Isomerization Catalyzed by Rhodium. Journal of the American Chemical Society. PMID 34415159 DOI: 10.1021/jacs.1c07230 |
0.422 |
|
| 2021 |
Schwartz LA, Spielmann K, Swyka RA, Xiang M, Krische MJ. Formate-Mediated Cross-Electrophile Reductive Coupling of Aryl Iodides and Bromopyridines. Israel Journal of Chemistry. 61: 198-301. PMID 34334805 DOI: 10.1002/ijch.202000069 |
0.314 |
|
| 2021 |
Santana CG, Krische MJ. From Hydrogenation to Transfer Hydrogenation to Hydrogen Auto-Transfer in Enantioselective Metal-Catalyzed Carbonyl Reductive Coupling: Past, Present, and Future. Acs Catalysis. 11: 5572-5585. PMID 34306816 DOI: 10.1021/acscatal.1c01109 |
0.392 |
|
| 2021 |
Siu YM, Roane J, Krische MJ. Total Synthesis of Leiodermatolide A via Transfer Hydrogenative Allylation, Crotylation, and Propargylation: Polyketide Construction beyond Discrete Allyl- or Allenylmetal Reagents. Journal of the American Chemical Society. PMID 34237219 DOI: 10.1021/jacs.1c06062 |
0.374 |
|
| 2021 |
Jung WO, Mai BK, Spinello BJ, Dubey ZJ, Kim SW, Stivala CE, Zbieg JR, Liu P, Krische MJ. Enantioselective Iridium-Catalyzed Allylation of Nitroalkanes: Entry to β-Stereogenic α-Quaternary Primary Amines. Journal of the American Chemical Society. PMID 34152145 DOI: 10.1021/jacs.1c05212 |
0.345 |
|
| 2021 |
Xiang M, Pfaffinger DE, Ortiz E, Brito GA, Krische MJ. Enantioselective Ruthenium-BINAP-Catalyzed Carbonyl Reductive Coupling of Alkoxyallenes: Convergent Construction of -Diols via ()-σ-Allylmetal Intermediates. Journal of the American Chemical Society. PMID 34060818 DOI: 10.1021/jacs.1c03480 |
0.41 |
|
| 2021 |
Krische MJ, Yoo M. Total Synthesis of the Spliceosome Modulator Pladienolide B via Asymmetric Alcohol-Mediated syn- and anti-Diastereoselective Carbonyl Crotylation. Angewandte Chemie (International Ed. in English). PMID 33794050 DOI: 10.1002/anie.202103845 |
0.351 |
|
| 2021 |
Doerksen RS, Hodík T, Hu G, Huynh NO, Shuler WG, Krische MJ. Ruthenium-Catalyzed Cycloadditions to Form Five-, Six-, and Seven-Membered Rings. Chemical Reviews. PMID 33576620 DOI: 10.1021/acs.chemrev.0c01133 |
0.38 |
|
| 2021 |
Xiang M, Ghosh A, Krische MJ. Diastereo- and Enantioselective Ruthenium-Catalyzed C-C Coupling of 1-Arylpropynes and Alcohols: Alkynes as Chiral Allylmetal Precursors in Carbonyl -(α-Aryl)allylation. Journal of the American Chemical Society. PMID 33555867 DOI: 10.1021/jacs.0c12242 |
0.463 |
|
| 2020 |
Krische MJ, Yang L, Wurm T, Poudel BS. Enantioselective Total Synthesis of Andrographolide and 14-Hydroxy-Colladonin: Carbonyl Reductive Coupling and trans-Decalin Formation via Hydrogen Transfer. Angewandte Chemie (International Ed. in English). PMID 32896046 DOI: 10.1002/Anie.202011363 |
0.519 |
|
| 2020 |
Krische MJ, Suravarapu SR, Parvathaneni SP, Bender JA, Roberts ST. Benzannulation via Ruthenium(0)-Catalyzed Transfer Hydrogenative Cycloaddition: Precision Synthesis and Photophysical Characterization of Soluble Diindenoperylenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32271965 DOI: 10.1002/Chem.202001731 |
0.796 |
|
| 2020 |
Meyer CC, Ortiz E, Krische MJ. Catalytic Reductive Aldol and Mannich Reactions of Enone, Acrylate, and Vinyl Heteroaromatic Pronucleophiles. Chemical Reviews. PMID 32191438 DOI: 10.1021/Acs.Chemrev.0C00053 |
0.44 |
|
| 2019 |
Tauber J, Schwartz LA, Krische MJ. Catalytic Enantioselective Synthesis of Chiral Organofluorine Compounds: Alcohol-Mediated Hydrogen Transfer for Catalytic Carbonyl Reductive Coupling. Organic Process Research & Development. 23: 730-736. PMID 32982140 DOI: 10.1021/acs.oprd.9b00035 |
0.39 |
|
| 2019 |
Kim SW, Meyer CC, Mai BK, Liu P, Krische MJ. Inversion of Enantioselectivity in Allene Gas versus Allyl Acetate Reductive Aldehyde Allylation Guided by Metal-Centered Stereogenicity: An Experimental and Computational Study. Acs Catalysis. 9: 9158-9163. PMID 31857913 DOI: 10.1021/Acscatal.9B03695 |
0.426 |
|
| 2019 |
Ambler BR, Woo SK, Krische MJ. Catalytic Enantioselective Carbonyl Propargylation Beyond Preformed Carbanions: Reductive Coupling and Hydrogen Auto-Transfer. Chemcatchem. 11: 324-332. PMID 31588251 DOI: 10.1002/Cctc.201801121 |
0.473 |
|
| 2019 |
Krische MJ, Brito G, Jung WO, Yoo M. Enantioselective Iridium-Catalyzed Allylation of Acetylenic Ketones via 2-Propanol-Mediated Reductive Coupling of Allyl Acetate: C14-C23 of Pladienolide D. Angewandte Chemie (International Ed. in English). PMID 31490591 DOI: 10.1002/Anie.201908939 |
0.499 |
|
| 2019 |
Spielmann K, Xiang M, Schwartz LA, Krische MJ. Direct Conversion of Primary Alcohols to 1,2-Amino Alcohols: Enantioselective Iridium-Catalyzed Carbonyl Reductive Coupling of Phthalimido-Allene via Hydrogen Auto-Transfer. Journal of the American Chemical Society. PMID 31465211 DOI: 10.1021/Jacs.9B08715 |
0.461 |
|
| 2019 |
Della-Felice F, Sarotti AM, Krische MJ, Pilli RA. Total Synthesis and Structural Validation of Phosdiecin A via Asymmetric Alcohol-Mediated Carbonyl Reductive Coupling. Journal of the American Chemical Society. PMID 31433167 DOI: 10.1021/Jacs.9B07512 |
0.432 |
|
| 2019 |
Krische MJ, Shuler WG, Swyka RA, Schempp TT, Spinello BJ. Vinyl Triflate-Aldehyde Reductive Coupling-Redox Isomerization Mediated by Formate: Rhodium-Catalyzed Ketone Synthesis in the Absence of Stoichiometric Metals. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31403727 DOI: 10.1002/Chem.201903668 |
0.504 |
|
| 2019 |
Krische MJ, Cabrera JM. Total Synthesis of Clavosolide A via Asymmetric Alcohol-Mediated Carbonyl Allylation: Beyond Protecting Groups or Chiral Auxiliaries in Polyketide Construction. Angewandte Chemie (International Ed. in English). PMID 31166641 DOI: 10.1002/Anie.201906259 |
0.42 |
|
| 2019 |
Doerksen RS, Meyer CC, Krische MJ. Feedstock Reagents in Metal-Catalyzed Carbonyl Reductive Coupling: Minimizing Preactivation for Efficiency in Target-Oriented Synthesis. Angewandte Chemie (International Ed. in English). PMID 31162793 DOI: 10.1002/Anie.201905532 |
0.501 |
|
| 2019 |
Krische MJ, Sato H, Blemker MA, Hellinghausen G, Armstrong DW, Nafie JW, Roberts ST. Triple Helical Ir(ppy)3 Phenylene Cage Prepared via Diol-Mediated Benzannulation: Synthesis, Resolution, Absolute Stereochemistry and Photophysical Properties. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31070822 DOI: 10.1002/Chem.201902122 |
0.341 |
|
| 2019 |
Swyka RA, Shuler WG, Spinello BJ, Zhang W, Lan C, Krische MJ. Conversion of Aldehydes to Branched or Linear Ketones via Regiodivergent Rhodium-Catalyzed Vinyl Bromide Reductive Coupling-Redox Isomerization Mediated by Formate. Journal of the American Chemical Society. PMID 30998328 DOI: 10.1021/Jacs.9B03113 |
0.482 |
|
| 2019 |
Kim SW, Schempp T, Zbieg J, Stivala C, Krische MJ, Kim SW. Regio- and Enantioselective Iridium-Catalyzed N-Allylation of Indoles and Related Azoles with Racemic Branched Alkyl-Substituted Allylic Acetates. Angewandte Chemie (International Ed. in English). PMID 30964961 DOI: 10.1002/Anie.201902799 |
0.44 |
|
| 2019 |
Luo G, Xiang M, Krische MJ. Successive Nucleophilic and Electrophilic Allylation for the Catalytic Enantioselective Synthesis of 2,4-Disubstituted Pyrrolidines. Organic Letters. PMID 30816719 DOI: 10.1021/Acs.Orglett.9B00508 |
0.516 |
|
| 2019 |
Swyka RA, Zhang W, Richardson J, Ruble JC, Krische MJ. Rhodium-Catalyzed Aldehyde Arylation via Formate-Mediated Transfer Hydrogenation: Beyond Metallic Reductants in Grignard/Nozaki-Hiyami-Kishi-Type Addition. Journal of the American Chemical Society. PMID 30693768 DOI: 10.1021/Jacs.8B13652 |
0.498 |
|
| 2019 |
Schwartz LA, Holmes M, Brito GA, Gonçalves TP, Richardson J, Ruble JC, Huang KW, Krische MJ. Cyclometalated Iridium-PhanePhos Complexes Are Active Catalysts in Enantioselective Allene-Fluoral Reductive Coupling and Related Alcohol-Mediated Carbonyl Additions That Form Acyclic Quaternary Carbon Stereocenters. Journal of the American Chemical Society. PMID 30681850 DOI: 10.1021/Jacs.8B11868 |
0.502 |
|
| 2019 |
Xiang M, Luo G, Wang Y, Krische MJ. Enantioselective iridium-catalyzed carbonyl isoprenylation via alcohol-mediated hydrogen transfer. Chemical Communications (Cambridge, England). PMID 30608076 DOI: 10.1039/C8Cc09706B |
0.514 |
|
| 2019 |
Tauber J, Schwartz LA, Krische MJ. Enantioselective Synthesis of Chiral Organofluorine Compounds: Alcohol-Mediated Hydrogen Transfer for Catalytic Carbonyl Reductive Coupling Organic Process Research & Development. 23: 730-736. DOI: 10.1021/Acs.Oprd.9B00035 |
0.489 |
|
| 2018 |
Kearney SE, Zahoránszky-Kőhalmi G, Brimacombe KR, Henderson MJ, Lynch C, Zhao T, Wan KK, Itkin Z, Dillon C, Shen M, Cheff DM, Lee TD, Bougie D, Cheng K, Coussens NP, ... ... Krische MJ, et al. Canvass: A Crowd-Sourced, Natural-Product Screening Library for Exploring Biological Space. Acs Central Science. 4: 1727-1741. PMID 30648156 DOI: 10.1021/Acscentsci.8B00747 |
0.599 |
|
| 2018 |
Kim SW, Schwartz LA, Zbieg JR, Stivala CE, Krische MJ. Regio- and Enantioselective Iridium-Catalyzed Amination of Racemic Branched Alkyl-Substituted Allylic Acetates with Primary and Secondary Aromatic and Heteroaromatic Amines. Journal of the American Chemical Society. PMID 30571092 DOI: 10.1021/Jacs.8B12152 |
0.466 |
|
| 2018 |
Kasun ZA, Sato H, Nie J, Mori Y, Bender JA, Roberts ST, Krische MJ. Alternating oligo(,-phenylenes) ruthenium catalyzed diol-diene benzannulation: orthogonality to cross-coupling enables nanographene and PAH construction. Chemical Science. 9: 7866-7873. PMID 30429996 DOI: 10.1039/C8Sc03236J |
0.394 |
|
| 2018 |
Cabrera JM, Tauber J, Zhang W, Xiang M, Krische MJ. Selection between Diastereomeric Kinetic vs Thermodynamic Carbonyl Binding Modes Enables Enantioselective Iridium-Catalyzed anti-(α-Aryl)allylation of Aqueous Fluoral Hydrate and Difluoroacetaldehyde Ethyl Hemiacetal. Journal of the American Chemical Society. PMID 30020777 DOI: 10.1021/Jacs.8B05725 |
0.426 |
|
| 2018 |
Ambler BR, Turnbull BWH, Suravarapu SR, Uteuliyev MM, Huynh NO, Krische MJ. Enantioselective Ruthenium-Catalyzed Benzocyclobutenone-Ketol Cycloaddition: Merging C-C Bond Activation and Transfer Hydrogenative Coupling for Type II Polyketide Construction. Journal of the American Chemical Society. PMID 29992811 DOI: 10.1021/Jacs.8B05724 |
0.845 |
|
| 2018 |
Kim SW, Wurm T, Brito GA, Jung WO, Zbieg JR, Stivala CE, Krische MJ. Hydroamination versus Allylic Amination in Iridium-Catalyzed Reactions of Allylic Acetates with Amines: 1,3-Aminoalcohols via Ester-Directed Regioselectivity. Journal of the American Chemical Society. PMID 29989803 DOI: 10.1021/Jacs.8B05683 |
0.478 |
|
| 2018 |
Brito GA, Della-Felice F, Luo G, Burns AS, Pilli RA, Rychnovsky SD, Krische MJ. Catalytic Enantioselective Allylations of Acetylenic Aldehydes via 2-Propanol-Mediated Reductive Coupling. Organic Letters. PMID 29938513 DOI: 10.1021/Acs.Orglett.8B01776 |
0.482 |
|
| 2018 |
Holmes M, Schwartz LA, Krische MJ. Intermolecular Metal-Catalyzed Reductive Coupling of Dienes, Allenes, and Enynes with Carbonyl Compounds and Imines. Chemical Reviews. PMID 29897740 DOI: 10.1021/Acs.Chemrev.8B00213 |
0.443 |
|
| 2018 |
Sato H, Bender JA, Roberts ST, Krische MJ. Helical Rod-like Phenylene Cages via Ruthenium Catalyzed Diol-Diene Benzannulation: A Cord of Three Strands. Journal of the American Chemical Society. PMID 29424530 DOI: 10.1021/Jacs.8B00131 |
0.349 |
|
| 2018 |
Meza AT, Wurm T, Smith L, Kim SW, Zbieg JR, Stivala CE, Krische MJ. Amphiphilic π-Allyliridium C,O-Benzoates Enable Regio- and Enantioselective Amination of Branched Allylic Acetates Bearing Linear Alkyl Groups. Journal of the American Chemical Society. PMID 29350523 DOI: 10.1021/Jacs.7B13482 |
0.443 |
|
| 2018 |
Sato H, Turnbull BWH, Fukaya K, Krische MJ. Ruthenium(0)-katalysierte Cycloaddition von 1,2-Diolen, Ketolen oder Dionen durch Alkohol-vermittelte Wasserstoffübertragung Angewandte Chemie. 130: 3064-3073. DOI: 10.1002/Ange.201709916 |
0.384 |
|
| 2017 |
Roane J, Holmes M, Krische MJ. Reductive C-C Coupling Hydrogenation and Transfer Hydrogenation: Departure from Stoichiometric Metals in Carbonyl Addition. Current Opinion in Green and Sustainable Chemistry. 7: 1-5. PMID 29726550 DOI: 10.1016/J.Cogsc.2017.06.006 |
0.493 |
|
| 2017 |
Krische MJ, Cabrera JM, Tauber J. Enantioselective Iridium Catalyzed Phthalide Formation via Internal Redox Allylation of Phthalaldehydes. Angewandte Chemie (International Ed. in English). PMID 29240280 DOI: 10.1002/Anie.201712015 |
0.411 |
|
| 2017 |
Roane J, Wippich J, Ramgren SD, Krische MJ. Synthesis of the C(1)-C(13) Fragment of Leiodermatolide via Hydrogen-Mediated C-C Bond Formation. Organic Letters. 19: 6634-6637. PMID 29168383 DOI: 10.1021/Acs.Orglett.7B03351 |
0.451 |
|
| 2017 |
Wurm T, Turnbull BWH, Ambler BR, Krische MJ. Thermal Hetero-Diels-Alder Reaction of Benzocyclobutenones with Isatins To Form 2-Oxindole Spirolactones. The Journal of Organic Chemistry. 82: 13751-13755. PMID 29164878 DOI: 10.1021/Acs.Joc.7B02769 |
0.329 |
|
| 2017 |
Krische MJ, Sato H, Turnbull BWH, Fukaya K. Ruthenium(0) Catalyzed Cycloaddition of 1,2-Diols, Ketols or Diones via Alcohol-Mediated Hydrogen Transfer. Angewandte Chemie (International Ed. in English). PMID 29068505 DOI: 10.1002/Anie.201709916 |
0.514 |
|
| 2017 |
Krische MJ, Sato H, Fukaya K, Sharma Poudel B. Diols as Dienophiles: Bridged Carbocycles via Ruthenium(0) Catalyzed Transfer Hydrogenative Cycloadditions of Cyclohexadiene or Norbornadiene. Angewandte Chemie (International Ed. in English). PMID 28941001 DOI: 10.1002/Anie.201708189 |
0.456 |
|
| 2017 |
Feng J, Holmes M, Krische MJ. Acyclic Quaternary Carbon Stereocenters via Enantioselective Transition Metal Catalysis. Chemical Reviews. PMID 28910092 DOI: 10.1021/Acs.Chemrev.7B00385 |
0.307 |
|
| 2017 |
Zhang W, Chen W, Xiao H, Krische MJ. Carbonyl anti-(α-Amino)allylation via Ruthenium Catalyzed Hydrogen Autotransfer: Use of an Acetylenic Pyrrole as an Allylmetal Pronucleophile. Organic Letters. PMID 28849663 DOI: 10.1021/Acs.Orglett.7B02336 |
0.507 |
|
| 2017 |
Bender M, Turnbull BWH, Ambler BR, Krische MJ. Ruthenium-catalyzed insertion of adjacent diol carbon atoms into C-C bonds: Entry to type II polyketides. Science (New York, N.Y.). 357: 779-781. PMID 28839069 DOI: 10.1126/Science.Aao0453 |
0.429 |
|
| 2017 |
Kim SW, Zhang W, Krische MJ. Catalytic Enantioselective Carbonyl Allylation and Propargylation via Alcohol-Mediated Hydrogen Transfer: Merging the Chemistry of Grignard and Sabatier. Accounts of Chemical Research. PMID 28792731 DOI: 10.1021/Acs.Accounts.7B00308 |
0.522 |
|
| 2017 |
Breit B, Haydl A, Lang T, Krische M. Alkynes as Electrophilic or Nucleophilic Allylmetal Precursors in Transition Metal Catalysis. Angewandte Chemie (International Ed. in English). PMID 28605083 DOI: 10.1002/Anie.201704248 |
0.797 |
|
| 2017 |
Holmes M, Nguyen KD, Schwartz LA, Luong T, Krische MJ. Enantioselective Formation of CF3-Bearing All-Carbon Quaternary Stereocenters via C-H Functionalization of Methanol: Iridium Catalyzed Allene Hydrohydroxymethylation. Journal of the American Chemical Society. PMID 28603973 DOI: 10.1021/Jacs.7B04374 |
0.451 |
|
| 2017 |
Guo YA, Liang T, Kim SW, Xiao H, Krische MJ. Nickel-Catalyzed Cross-Coupling of Vinyl Dioxanones to Form Enantiomerically Enriched Cyclopropanes. Journal of the American Chemical Society. PMID 28489371 DOI: 10.1021/Jacs.7B03371 |
0.402 |
|
| 2017 |
Kim SW, Lee W, Krische MJ. Asymmetric Allylation of Glycidols Mediated by Allyl Acetate via Iridium-Catalyzed Hydrogen Transfer. Organic Letters. PMID 28221810 DOI: 10.1021/Acs.Orglett.7B00343 |
0.533 |
|
| 2017 |
Luong T, Chen S, Qu K, McInturff EL, Krische MJ. Ruthenium(0)-Catalyzed C-C Coupling of Alkynes and 3-Hydroxy-2-oxindoles: Direct C-H Vinylation of Alcohols. Organic Letters. PMID 28164712 DOI: 10.1021/Acs.Orglett.7B00174 |
0.479 |
|
| 2017 |
Schwartz LA, Krische MJ. Hydrogen-Mediated C−C Bond Formation: Stereo- and Site-Selective Chemical Synthesis Beyond Stoichiometric Organometallic Reagents Israel Journal of Chemistry. 58: 45-51. DOI: 10.1002/Ijch.201700088 |
0.415 |
|
| 2017 |
Haydl AM, Breit B, Liang T, Krische MJ. Alkine als alternativer Einstieg in elektrophile und nukleophile Übergangsmetall-katalysierte Allylierungen Angewandte Chemie. 129: 11466-11480. DOI: 10.1002/Ange.201704248 |
0.745 |
|
| 2016 |
Oda S, Franke J, Krische MJ. Diene hydroaminomethylation ruthenium-catalyzed C-C bond forming transfer hydrogenation: beyond carbonylation. Chemical Science. 7: 136-141. PMID 29861974 DOI: 10.1039/C5Sc03854E |
0.697 |
|
| 2016 |
Krische MJ, Guo YA, Lee W. Enantioselective Synthesis of Oxetanes Bearing All-Carbon Quaternary Stereocenters via Iridium Catalyzed C-C Bond Forming Transfer Hydrogenation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28039892 DOI: 10.1002/Chem.201606046 |
0.527 |
|
| 2016 |
Sato H, Bender M, Chen W, Krische MJ. Diols, α-Ketols, and Diones as 22π Components in [2+2+2] Cycloadditions of 1,6-Diynes via Ruthenium(0)-Catalyzed Transfer Hydrogenation. Journal of the American Chemical Society. PMID 27933983 DOI: 10.1021/Jacs.6B11746 |
0.451 |
|
| 2016 |
Xiao H, Wang G, Krische MJ. Regioselective Hydrohydroxyalkylation of Styrene with Primary Alcohols or Aldehydes via Ruthenium-Catalyzed C-C Bond Forming Transfer Hydrogenation. Angewandte Chemie (International Ed. in English). PMID 27910228 DOI: 10.1002/Anie.201609056 |
0.491 |
|
| 2016 |
Nguyen KD, Park BY, Luong T, Sato H, Garza VJ, Krische MJ. Metal-catalyzed reductive coupling of olefin-derived nucleophiles: Reinventing carbonyl addition. Science (New York, N.Y.). 354. PMID 27846504 DOI: 10.1126/Science.Aah5133 |
0.519 |
|
| 2016 |
Shin I, Hong S, Krische MJ. Total Synthesis of Swinholide A: An Exposition in Hydrogen-Mediated C-C Bond Formation. Journal of the American Chemical Society. PMID 27779393 DOI: 10.1021/Jacs.6B10645 |
0.466 |
|
| 2016 |
Nguyen KD, Herkommer D, Krische MJ. Enantioselective Formation of All-Carbon Quaternary Centers via C-H Functionalization of Methanol: Iridium-Catalyzed Diene Hydrohydroxymethylation. Journal of the American Chemical Society. PMID 27762549 DOI: 10.1021/Jacs.6B09333 |
0.818 |
|
| 2016 |
Ketcham JM, Volchkov I, Chen TY, Blumberg PM, Kedei N, Lewin NE, Krische MJ. Evaluation of Chromane-Based Bryostatin Analogues Prepared via Hydrogen-Mediated C-C Bond Formation: Potency Does Not Confer Bryostatin-like Biology. Journal of the American Chemical Society. PMID 27676096 DOI: 10.1021/Jacs.6B08695 |
0.4 |
|
| 2016 |
Feng J, Noack F, Krische MJ. Modular Terpenoid Construction via Catalytic Enantioselective Formation of All-Carbon Quaternary Centers: Total Synthesis of Oridamycin A, Triptoquinones B and C, and Isoiresin. Journal of the American Chemical Society. PMID 27632643 DOI: 10.1021/Jacs.6B08902 |
0.455 |
|
| 2016 |
Park BY, Luong T, Sato H, Krische MJ. Osmium(0) Catalyzed C-C Coupling of Ethylene and alpha-Olefins with Diols, Ketols or Hydroxy Esters via Transfer Hydrogenation. The Journal of Organic Chemistry. PMID 27580269 DOI: 10.1021/Acs.Joc.6B01923 |
0.461 |
|
| 2016 |
Perez F, Oda S, Geary LM, Krische MJ. Ruthenium-Catalyzed Transfer Hydrogenation for C-C Bond Formation: Hydrohydroxyalkylation and Hydroaminoalkylation via Reactant Redox Pairs. Topics in Current Chemistry (Journal). 374: 35. PMID 27573275 DOI: 10.1007/S41061-016-0028-0 |
0.711 |
|
| 2016 |
Wang G, Krische MJ. Total Synthesis of (+)-SCH 351448: Efficiency via Chemoselectivity and Redox-Economy Powered by Metal Catalysis. Journal of the American Chemical Society. PMID 27337561 DOI: 10.1021/Jacs.6B04917 |
0.371 |
|
| 2016 |
Liang T, Woo SK, Krische MJ. C-Propargylation Overrides O-Propargylation in Reactions of Propargyl Chloride with Primary Alcohols: Rhodium-Catalyzed Transfer Hydrogenation. Angewandte Chemie (International Ed. in English). PMID 27321353 DOI: 10.1002/Anie.201603575 |
0.483 |
|
| 2016 |
Hong S, Krische MJ. Beyond Protecting Groups in Metal Catalyzed C-C Coupling: Direct Anomeric Propargylation of Aldoses. Acs Central Science. 2: 12-3. PMID 27163021 DOI: 10.1021/Acscentsci.6B00002 |
0.379 |
|
| 2016 |
Feng J, Kasun ZA, Krische MJ. Enantioselective Alcohol C-H Functionalization for Polyketide Construction: Unlocking Redox-Economy and Site-Selectivity for Ideal Chemical Synthesis. Journal of the American Chemical Society. PMID 27113543 DOI: 10.1021/Jacs.6B02019 |
0.467 |
|
| 2016 |
Perez F, Waldeck AR, Krische MJ. Total Synthesis of Cryptocaryol A by Enantioselective Iridium-Catalyzed Alcohol C-H Allylation. Angewandte Chemie (International Ed. in English). 55: 5049-52. PMID 27079820 DOI: 10.1002/Anie.201600591 |
0.494 |
|
| 2016 |
Nguyen KD, Herkommer D, Krische MJ. Ruthenium-BINAP Catalyzed Alcohol C-H tert-Prenylation via 1,3-Enyne Transfer Hydrogenation: Beyond Stoichiometric Carbanions in Enantioselective Carbonyl Propargylation. Journal of the American Chemical Society. PMID 27079149 DOI: 10.1021/Jacs.6B02279 |
0.822 |
|
| 2016 |
Garza VJ, Krische MJ. Hydroxymethylation beyond Carbonylation: Enantioselective Iridium-Catalyzed Reductive Coupling of Formaldehyde with Allylic Acetates via Enantiotopic π-Facial Discrimination. Journal of the American Chemical Society. PMID 26958737 DOI: 10.1021/Jacs.6B01078 |
0.488 |
|
| 2016 |
Perez F, Waldeck AR, Krische MJ. Total Synthesis of Cryptocaryol A by Enantioselective Iridium-Catalyzed Alcohol C-H Allylation Angewandte Chemie - International Edition. DOI: 10.1002/anie.201600591 |
0.342 |
|
| 2015 |
Jo HH, Gao X, You L, Anslyn EV, Krische MJ. Application of a High-Throughput Enantiomeric Excess Optical Assay Involving a Dynamic Covalent Assembly: Parallel Asymmetric Allylation and Ee Sensing of Homoallylic Alcohols. Chemical Science (Royal Society of Chemistry : 2010). 6: 6747-6753. PMID 27014433 DOI: 10.1039/C5Sc02416A |
0.531 |
|
| 2015 |
Liang T, Zhang W, Krische MJ. Iridium-Catalyzed C-C Coupling of a Simple Propargyl Ether with Primary Alcohols: Enantioselective Homoaldol Addition via Redox-Triggered (Z)-Siloxyallylation. Journal of the American Chemical Society. PMID 26671223 DOI: 10.1021/Jacs.5B12131 |
0.518 |
|
| 2015 |
Saxena A, Perez F, Krische MJ. Ruthenium(0)-Catalyzed [4+2] Cycloaddition of Acetylenic Aldehydes with α-Ketols: Convergent Construction of Angucycline Ring Systems. Angewandte Chemie (International Ed. in English). PMID 26663806 DOI: 10.1002/Anie.201509646 |
0.403 |
|
| 2015 |
Liang T, Zhang W, Chen TY, Nguyen KD, Krische MJ. Ruthenium Catalyzed Diastereo- and Enantioselective Coupling of Propargyl Ethers with Alcohols: Siloxy-Crotylation via Hydride Shift Enabled Conversion of Alkynes to π-Allyls. Journal of the American Chemical Society. PMID 26418572 DOI: 10.1021/Jacs.5B08019 |
0.477 |
|
| 2015 |
Shin I, Krische MJ. Formal Synthesis of Premisakinolide A and C(19)-C(32) of Swinholide A via Site-Selective C-H Allylation and Crotylation of Unprotected Diols. Organic Letters. 17: 4686-9. PMID 26375150 DOI: 10.1021/Acs.Orglett.5B02056 |
0.401 |
|
| 2015 |
Shin I, Ramgren SD, Krische MJ. Reductive Cyclization of Halo-Ketones to Form 3-Hydroxy-2-Oxindoles via Palladium Catalyzed Hydrogenation: A Hydrogen-Mediated Grignard Addition. Tetrahedron. 71: 5776-5780. PMID 26273111 DOI: 10.1016/J.Tet.2015.05.085 |
0.483 |
|
| 2015 |
Tsutsumi R, Hong S, Krische MJ. Diastereo- and Enantioselective Iridium Catalyzed Carbonyl (α-Cyclopropyl)allylation via Transfer Hydrogenation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26235369 DOI: 10.1002/Chem.201502499 |
0.475 |
|
| 2015 |
Shin I, Krische MJ. Asymmetric Iridium-Catalyzed C-C Coupling of Chiral Diols via Site-Selective Redox-Triggered Carbonyl Addition. Topics in Current Chemistry. PMID 26187028 DOI: 10.1007/128_2015_651 |
0.498 |
|
| 2015 |
Kasun ZA, Gao X, Lipinski RM, Krische MJ. Direct Generation of Triketide Stereopolyads via Merged Redox-Construction Events: Total Synthesis of (+)-Zincophorin Methyl Ester. Journal of the American Chemical Society. PMID 26167950 DOI: 10.1021/Jacs.5B05296 |
0.44 |
|
| 2015 |
Grayson MN, Krische MJ, Houk KN. Ruthenium-Catalyzed Asymmetric Hydrohydroxyalkylation of Butadiene: The Role of the Formyl Hydrogen Bond in Stereochemical Control. Journal of the American Chemical Society. PMID 26107070 DOI: 10.1021/Jacs.5B04844 |
0.473 |
|
| 2015 |
Wang G, Franke J, Ngo CQ, Krische MJ. Diastereo- and Enantioselective Iridium Catalyzed Coupling of Vinyl Aziridines with Alcohols: Site-Selective Modification of Unprotected Diols and Synthesis of Substituted Piperidines. Journal of the American Chemical Society. 137: 7915-20. PMID 26074091 DOI: 10.1021/Jacs.5B04404 |
0.44 |
|
| 2015 |
Park BY, Luong T, Sato H, Krische MJ. A Metallacycle Fragmentation Strategy for Vinyl Transfer from Enol Carboxylates to Secondary Alcohol C-H Bonds via Osmium- or Ruthenium-Catalyzed Transfer Hydrogenation. Journal of the American Chemical Society. 137: 7652-5. PMID 26066660 DOI: 10.1021/Jacs.5B04688 |
0.509 |
|
| 2015 |
Oda S, Sam B, Krische MJ. Hydroaminomethylation Beyond Carbonylation: Allene-Imine Reductive Coupling by Ruthenium-Catalyzed Transfer Hydrogenation. Angewandte Chemie (International Ed. in English). 54: 8525-8528. PMID 26031224 DOI: 10.1002/Anie.201503250 |
0.663 |
|
| 2015 |
Saxena A, Perez F, Krische MJ. Ruthenium(0) Catalyzed Endiyne-α-Ketol [4 + 2] Cycloaddition: Convergent Assembly of Type II Polyketide Substructures via C-C Bond Forming Transfer Hydrogenation. Journal of the American Chemical Society. 137: 5883-6. PMID 25938947 DOI: 10.1021/Jacs.5B02755 |
0.465 |
|
| 2015 |
Sam B, Luong T, Krische MJ. Ruthenium-catalyzed C-C coupling of fluorinated alcohols with allenes: dehydrogenation at the energetic limit of β-hydride elimination. Angewandte Chemie (International Ed. in English). 54: 5465-9. PMID 25757459 DOI: 10.1002/Anie.201500238 |
0.425 |
|
| 2015 |
Liang T, Nguyen KD, Zhang W, Krische MJ. Enantioselective ruthenium-catalyzed carbonyl allylation via alkyne-alcohol C-C bond-forming transfer hydrogenation: allene hydrometalation vs oxidative coupling. Journal of the American Chemical Society. 137: 3161-4. PMID 25734220 DOI: 10.1021/Jacs.5B00747 |
0.522 |
|
| 2015 |
Chen TY, Tsutsumi R, Montgomery TP, Volchkov I, Krische MJ. Ruthenium-catalyzed C-C coupling of amino alcohols with dienes via transfer hydrogenation: redox-triggered imine addition and related hydroaminoalkylations. Journal of the American Chemical Society. 137: 1798-801. PMID 25642996 DOI: 10.1021/Ja5130258 |
0.55 |
|
| 2015 |
Sam B, Breit B, Krische MJ. Paraformaldehyde and methanol as C1 feedstocks in metal-catalyzed C-C couplings of π-unsaturated reactants: beyond hydroformylation. Angewandte Chemie (International Ed. in English). 54: 3267-74. PMID 25430585 DOI: 10.1002/Anie.201407888 |
0.644 |
|
| 2015 |
Oda S, Franke J, Krische MJ. Diene hydroaminomethylation via ruthenium-catalyzed C-C bond forming transfer hydrogenation: Beyond carbonylation Chemical Science. 7: 136-141. DOI: 10.1039/c5sc03854e |
0.361 |
|
| 2015 |
Shin I, Ramgren SD, Krische MJ. Reductive cyclization of halo-ketones to form 3-hydroxy-2-oxindoles via palladium catalyzed hydrogenation: a hydrogen-mediated Grignard addition Tetrahedron. 71: 5776-5780. DOI: 10.1016/j.tet.2015.05.085 |
0.367 |
|
| 2014 |
Andrews IP, Ketcham JM, Blumberg PM, Kedei N, Lewin NE, Peach ML, Krische MJ. Synthesis of seco-B-ring bryostatin analogue WN-1 via C-C bond-forming hydrogenation: critical contribution of the B-ring in determining bryostatin-like and phorbol 12-myristate 13-acetate-like properties. Journal of the American Chemical Society. 136: 13209-16. PMID 25207655 DOI: 10.1021/Ja507825S |
0.445 |
|
| 2014 |
Shin I, Wang G, Krische MJ. Catalyst-directed diastereo- and site-selectivity in successive nucleophilic and electrophilic allylations of chiral 1,3-diols: protecting-group-free synthesis of substituted pyrans. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 13382-9. PMID 25169904 DOI: 10.1002/Chem.201404065 |
0.461 |
|
| 2014 |
Park BY, Nguyen KD, Chaulagain MR, Komanduri V, Krische MJ. Alkynes as allylmetal equivalents in redox-triggered C-C couplings to primary alcohols: (Z)-homoallylic alcohols via ruthenium-catalyzed propargyl C-H oxidative addition. Journal of the American Chemical Society. 136: 11902-5. PMID 25075434 DOI: 10.1021/Ja505962W |
0.434 |
|
| 2014 |
Ketcham JM, Shin I, Montgomery TP, Krische MJ. Catalytic enantioselective C-H functionalization of alcohols by redox-triggered carbonyl addition: borrowing hydrogen, returning carbon. Angewandte Chemie (International Ed. in English). 53: 9142-50. PMID 25056771 DOI: 10.1002/Anie.201403873 |
0.505 |
|
| 2014 |
Feng J, Garza VJ, Krische MJ. Redox-triggered C-C coupling of alcohols and vinyl epoxides: diastereo- and enantioselective formation of all-carbon quaternary centers via tert-(hydroxy)-prenylation. Journal of the American Chemical Society. 136: 8911-4. PMID 24915473 DOI: 10.1021/Ja504625M |
0.483 |
|
| 2014 |
Kasun ZA, Geary LM, Krische MJ. Ring expansion of cyclic 1,2-diols to form medium sized rings via ruthenium catalyzed transfer hydrogenative [4+2] cycloaddition. Chemical Communications (Cambridge, England). 50: 7545-7. PMID 24890278 DOI: 10.1039/C4Cc03983A |
0.4 |
|
| 2014 |
Geary LM, Chen TY, Montgomery TP, Krische MJ. Benzannulation via ruthenium-catalyzed diol-diene [4+2] cycloaddition: one- and two-directional syntheses of fluoranthenes and acenes. Journal of the American Chemical Society. 136: 5920-2. PMID 24724733 DOI: 10.1021/Ja502659T |
0.414 |
|
| 2014 |
McInturff EL, Nguyen KD, Krische MJ. Redox-triggered C-C coupling of diols and alkynes: synthesis of β,γ-unsaturated α-hydroxyketones and furans by ruthenium-catalyzed hydrohydroxyalkylation. Angewandte Chemie (International Ed. in English). 53: 3232-5. PMID 24677357 DOI: 10.1002/Anie.201311130 |
0.461 |
|
| 2014 |
Dechert-Schmitt AM, Schmitt DC, Gao X, Itoh T, Krische MJ. Polyketide construction via hydrohydroxyalkylation and related alcohol C-H functionalizations: reinventing the chemistry of carbonyl addition. Natural Product Reports. 31: 504-13. PMID 24514754 DOI: 10.1039/C3Np70076C |
0.575 |
|
| 2014 |
Itoh T, Montgomery TP, Recio A, Krische MJ. Asymmetric alcohol C-H allylation and syn-crotylation: C9-C20 of tetrafibricin. Organic Letters. 16: 820-3. PMID 24422777 DOI: 10.1021/Ol403566W |
0.436 |
|
| 2014 |
Smuts JP, Hao XQ, Han Z, Parpia C, Krische MJ, Armstrong DW. Enantiomeric separations of chiral sulfonic and phosphoric acids with barium-doped cyclofructan selectors via an ion interaction mechanism. Analytical Chemistry. 86: 1282-90. PMID 24372088 DOI: 10.1021/Ac403686A |
0.331 |
|
| 2014 |
Swager TM, Koo B, Geary LM, Chen T-, Montgomery TP, Krische MJ. Fluoranthenes and Acenes Synthesized from Diol–Diene Cycloaddition Synfacts. 10: 699-699. DOI: 10.1055/S-0033-1340200 |
0.355 |
|
| 2014 |
Sam B, Breit B, Krische MJ. Paraformaldehyd und Methanol als C1-Rohstoffe in metallkatalysierten C-C-Kupplungen π-ungesättigter Edukte Angewandte Chemie. 127: 3317-3325. DOI: 10.1002/Ange.201407888 |
0.536 |
|
| 2014 |
Ketcham JM, Shin I, Montgomery TP, Krische MJ. Katalytische enantioselektive C-H-Funktionalisierung von Alkoholen durch redoxgesteuerte Addition an die Carbonylgruppe: Wasserstoff-Ausleihe und Kohlenstoff-Rückgabe Angewandte Chemie. 126: 9294-9302. DOI: 10.1002/Ange.201403873 |
0.363 |
|
| 2013 |
McInturff EL, Mowat J, Waldeck AR, Krische MJ. Ruthenium-catalyzed hydrohydroxyalkylation of acrylates with diols and α-hydroxycarbonyl compounds to form spiro- and α-methylene-γ-butyrolactones. Journal of the American Chemical Society. 135: 17230-5. PMID 24187991 DOI: 10.1021/Ja410533Y |
0.379 |
|
| 2013 |
Park BY, Montgomery TP, Garza VJ, Krische MJ. Ruthenium catalyzed hydrohydroxyalkylation of isoprene with heteroaromatic secondary alcohols: isolation and reversible formation of the putative metallacycle intermediate. Journal of the American Chemical Society. 135: 16320-3. PMID 24156560 DOI: 10.1021/Ja4087193 |
0.407 |
|
| 2013 |
Del Valle DJ, Krische MJ. Total synthesis of (+)-trienomycins A and F via C-C bond-forming hydrogenation and transfer hydrogenation. Journal of the American Chemical Society. 135: 10986-9. PMID 23862627 DOI: 10.1021/Ja4061273 |
0.503 |
|
| 2013 |
Sam B, Montgomery TP, Krische MJ. Ruthenium catalyzed reductive coupling of paraformaldehyde to trifluoromethyl allenes: CF3-bearing all-carbon quaternary centers. Organic Letters. 15: 3790-3. PMID 23841678 DOI: 10.1021/Ol401771A |
0.386 |
|
| 2013 |
Yamaguchi E, Mowat J, Luong T, Krische MJ. Regio- and diastereoselective C-C coupling of α-olefins and styrenes to 3-hydroxy-2-oxindoles by Ru-catalyzed hydrohydroxyalkylation. Angewandte Chemie (International Ed. in English). 52: 8428-31. PMID 23832830 DOI: 10.1002/Anie.201303552 |
0.58 |
|
| 2013 |
Schmitt DC, Lee J, Dechert-Schmitt AM, Yamaguchi E, Krische MJ. Ruthenium catalyzed hydroaminoalkylation of isoprene via transfer hydrogenation: byproduct-free prenylation of hydantoins. Chemical Communications (Cambridge, England). 49: 6096-8. PMID 23722271 DOI: 10.1039/C3Cc43463J |
0.523 |
|
| 2013 |
Chen TY, Krische MJ. Regioselective ruthenium catalyzed hydrohydroxyalkylation of dienes with 3-hydroxy-2-oxindoles: prenylation, geranylation, and beyond. Organic Letters. 15: 2994-7. PMID 23721207 DOI: 10.1021/Ol401184K |
0.517 |
|
| 2013 |
Waldeck AR, Krische MJ. Total synthesis of cyanolide A in the absence of protecting groups, chiral auxiliaries, or premetalated carbon nucleophiles. Angewandte Chemie (International Ed. in English). 52: 4470-3. PMID 23495211 DOI: 10.1002/Anie.201300843 |
0.315 |
|
| 2013 |
Gao X, Woo SK, Krische MJ. Total synthesis of 6-deoxyerythronolide B via C-C bond-forming transfer hydrogenation. Journal of the American Chemical Society. 135: 4223-6. PMID 23464668 DOI: 10.1021/Ja4008722 |
0.548 |
|
| 2013 |
Geary LM, Glasspoole BW, Kim MM, Krische MJ. Successive C-C coupling of dienes to vicinally dioxygenated hydrocarbons: ruthenium catalyzed [4 + 2] cycloaddition across the diol, hydroxycarbonyl, or dione oxidation levels. Journal of the American Chemical Society. 135: 3796-9. PMID 23448269 DOI: 10.1021/Ja400691T |
0.465 |
|
| 2013 |
Dechert-Schmitt AM, Schmitt DC, Krische MJ. Protecting-group-free diastereoselective C-C coupling of 1,3-glycols and allyl acetate through site-selective primary alcohol dehydrogenation. Angewandte Chemie (International Ed. in English). 52: 3195-8. PMID 23364927 DOI: 10.1002/Anie.201209863 |
0.4 |
|
| 2013 |
Waldeck AR, Krische MJ. Total Synthesis of Cyanolide A Synfacts. 9: 583-583. DOI: 10.1055/S-0033-1338717 |
0.326 |
|
| 2013 |
Köpfer A, Sam B, Breit B, Krische MJ. Regiodivergent reductive coupling of 2-substituted dienes to formaldehyde employing ruthenium or nickel catalyst: Hydrohydroxymethylation via transfer hydrogenation Chemical Science. 4: 1876-1880. DOI: 10.1039/C3Sc22051F |
0.671 |
|
| 2013 |
Yamaguchi E, Mowat J, Luong T, Krische MJ. ChemInform Abstract: Regio- and Diastereoselective C-C Coupling of α-Olefins and Styrenes to 3-Hydroxy-2-oxindoles by Ru-Catalyzed Hydrohydroxyalkylation. Cheminform. 45: no-no. DOI: 10.1002/chin.201401125 |
0.329 |
|
| 2013 |
Moran J, Krische MJ. Enantioselective Carbonyl Allylation and Crotylation from the Alcohol Oxidation Level via C-C Bond Forming Transfer Hydrogenation Asymmetric Synthesis Ii: More Methods and Applications. 187-196. DOI: 10.1002/9783527652235.ch24 |
0.388 |
|
| 2012 |
Moran J, Krische MJ. Formation of C-C bonds via ruthenium-catalyzed transfer hydrogenation(). Pure and Applied Chemistry. Chimie Pure Et Appliquee. 84: 1729-1739. PMID 23430602 DOI: 10.1351/Pac-Con-11-10-18 |
0.708 |
|
| 2012 |
McInturff EL, Yamaguchi E, Krische MJ. Chiral-anion-dependent inversion of diastereo- and enantioselectivity in carbonyl crotylation via ruthenium-catalyzed butadiene hydrohydroxyalkylation. Journal of the American Chemical Society. 134: 20628-31. PMID 23234459 DOI: 10.1021/Ja311208A |
0.404 |
|
| 2012 |
Schmitt DC, Dechert-Schmitt AM, Krische MJ. Iridium-catalyzed allylation of chiral β-stereogenic alcohols: bypassing discrete formation of epimerizable aldehydes. Organic Letters. 14: 6302-5. PMID 23231774 DOI: 10.1021/Ol3030692 |
0.469 |
|
| 2012 |
Geary LM, Leung JC, Krische MJ. Ruthenium-catalyzed reductive coupling of 1,3-enynes and aldehydes by transfer hydrogenation: anti-diastereoselective carbonyl propargylation. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 16823-7. PMID 23147989 DOI: 10.1002/Chem.201202446 |
0.444 |
|
| 2012 |
Leung JC, Geary LM, Chen TY, Zbieg JR, Krische MJ. Direct, redox-neutral prenylation and geranylation of secondary carbinol C-H bonds: C4-regioselectivity in ruthenium-catalyzed C-C couplings of dienes to α-hydroxy esters. Journal of the American Chemical Society. 134: 15700-3. PMID 22985393 DOI: 10.1021/Ja3075049 |
0.488 |
|
| 2012 |
Woo SK, Geary LM, Krische MJ. Enantioselective carbonyl propargylation by iridium-catalyzed transfer hydrogenative coupling of alcohols and propargyl chlorides. Angewandte Chemie (International Ed. in English). 51: 7830-4. PMID 22736416 DOI: 10.1002/Anie.201203334 |
0.493 |
|
| 2012 |
Montgomery TP, Hassan A, Park BY, Krische MJ. Enantioselective conversion of primary alcohols to α-exo-methylene γ-butyrolactones via iridium-catalyzed C-C bond-forming transfer hydrogenation: 2-(alkoxycarbonyl)allylation. Journal of the American Chemical Society. 134: 11100-3. PMID 22734694 DOI: 10.1021/Ja303839H |
0.533 |
|
| 2012 |
Hassan A, Montgomery TP, Krische MJ. Consecutive iridium catalyzed C-C and C-H bond forming hydrogenations for the diastereo- and enantioselective synthesis of syn-3-fluoro-1-alcohols: C-H (2-fluoro)allylation of primary alcohols. Chemical Communications (Cambridge, England). 48: 4692-4. PMID 22473044 DOI: 10.1039/C2Cc31743E |
0.492 |
|
| 2012 |
Zbieg JR, Yamaguchi E, McInturff EL, Krische MJ. Enantioselective C-H crotylation of primary alcohols via hydrohydroxyalkylation of butadiene. Science (New York, N.Y.). 336: 324-7. PMID 22442385 DOI: 10.1126/Science.1219274 |
0.42 |
|
| 2012 |
Geary LM, Woo SK, Leung JC, Krische MJ. Diastereo- and enantioselective iridium-catalyzed carbonyl propargylation from the alcohol or aldehyde oxidation level: 1,3-enynes as allenylmetal equivalents. Angewandte Chemie (International Ed. in English). 51: 2972-6. PMID 22337340 DOI: 10.1002/Anie.201200239 |
0.394 |
|
| 2012 |
Leung JC, Krische MJ. Catalytic intermolecular hydroacylation of C-C π-bonds in the absence of chelation assistance Chemical Science. 3: 2202-2209. DOI: 10.1039/C2Sc20350B |
0.463 |
|
| 2012 |
Krische MJ, Jang HY. 4.6 C-C Bond Formation (Metal-Catalyzed Reductive Aldol Coupling) Comprehensive Chirality. 4: 100-121. DOI: 10.1016/B978-0-08-095167-6.00405-5 |
0.59 |
|
| 2011 |
Hassan A, Krische MJ. Unlocking Hydrogenation for C-C Bond Formation: A Brief Overview of Enantioselective Methods. Organic Process Research & Development. 15: 1236-1242. PMID 22125398 DOI: 10.1021/Op200195M |
0.507 |
|
| 2011 |
Moran J, Smith AG, Carris RM, Johnson JS, Krische MJ. Polarity inversion of donor-acceptor cyclopropanes: disubstituted δ-lactones via enantioselective iridium catalysis. Journal of the American Chemical Society. 133: 18618-21. PMID 22026505 DOI: 10.1021/Ja2090993 |
0.679 |
|
| 2011 |
Leung JC, Patman RL, Sam B, Krische MJ. Alkyne-aldehyde reductive C-C coupling through ruthenium-catalyzed transfer hydrogenation: direct regio- and stereoselective carbonyl vinylation to form trisubstituted allylic alcohols in the absence of premetallated reagents. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 12437-43. PMID 21953608 DOI: 10.1002/Chem.201101554 |
0.839 |
|
| 2011 |
Hassan A, Townsend IA, Krische MJ. Catalytic enantioselective Grignard Nozaki-Hiyama methallylation from the alcohol oxidation level: chloride compensates for π-complex instability. Chemical Communications (Cambridge, England). 47: 10028-30. PMID 21829853 DOI: 10.1039/C1Cc14392A |
0.486 |
|
| 2011 |
Bower JF, Krische MJ. Formation of C-C Bonds via Iridium-Catalyzed Hydrogenation and Transfer Hydrogenation. Topics in Organometallic Chemistry. 34: 107-138. PMID 21822399 DOI: 10.1007/978-3-642-15334-1_5 |
0.726 |
|
| 2011 |
Lu Y, Woo SK, Krische MJ. Total synthesis of bryostatin 7 via C-C bond-forming hydrogenation. Journal of the American Chemical Society. 133: 13876-9. PMID 21780806 DOI: 10.1021/Ja205673E |
0.463 |
|
| 2011 |
Gao X, Han H, Krische MJ. Direct generation of acyclic polypropionate stereopolyads via double diastereo- and enantioselective iridium-catalyzed crotylation of 1,3-diols: beyond stepwise carbonyl addition in polyketide construction. Journal of the American Chemical Society. 133: 12795-800. PMID 21739988 DOI: 10.1021/Ja204570W |
0.582 |
|
| 2011 |
Zbieg JR, Moran J, Krische MJ. Diastereo- and enantioselective ruthenium-catalyzed hydrohydroxyalkylation of 2-silyl-butadienes: carbonyl syn-crotylation from the alcohol oxidation level. Journal of the American Chemical Society. 133: 10582-6. PMID 21627316 DOI: 10.1021/Ja2046028 |
0.629 |
|
| 2011 |
Bausch CC, Patman RL, Breit B, Krische MJ. Divergent regioselectivity in the synthesis of trisubstituted allylic alcohols by nickel- and ruthenium-catalyzed alkyne hydrohydroxymethylation with formaldehyde. Angewandte Chemie (International Ed. in English). 50: 5687-90. PMID 21557426 DOI: 10.1002/Anie.201101496 |
0.818 |
|
| 2011 |
Gao X, Zhang YJ, Krische MJ. Iridium-catalyzed anti-diastereo- and enantioselective carbonyl (α-trifluoromethyl)allylation from the alcohol or aldehyde oxidation level. Angewandte Chemie (International Ed. in English). 50: 4173-5. PMID 21472938 DOI: 10.1002/Anie.201008296 |
0.548 |
|
| 2011 |
Kumpulainen ET, Kang B, Krische MJ. C(21)-C(40) of tetrafibricin via metal catalysis: beyond stoichiometric chiral reagents, auxiliaries, and premetalated nucleophiles. Organic Letters. 13: 2484-7. PMID 21469726 DOI: 10.1021/Ol200735R |
0.457 |
|
| 2011 |
Moran J, Preetz A, Mesch RA, Krische MJ. Iridium-catalysed direct C-C coupling of methanol and allenes. Nature Chemistry. 3: 287-90. PMID 21430686 DOI: 10.1038/Nchem.1001 |
0.659 |
|
| 2011 |
Hassan A, Zbieg JR, Krische MJ. Enantioselective iridium-catalyzed vinylogous Reformatsky-aldol reaction from the alcohol oxidation level: linear regioselectivity by way of carbon-bound enolates. Angewandte Chemie (International Ed. in English). 50: 3493-6. PMID 21381171 DOI: 10.1002/Anie.201100646 |
0.546 |
|
| 2011 |
Gao X, Townsend IA, Krische MJ. Enhanced anti-diastereo- and enantioselectivity in alcohol-mediated carbonyl crotylation using an isolable single component iridium catalyst. The Journal of Organic Chemistry. 76: 2350-4. PMID 21375283 DOI: 10.1021/Jo200068Q |
0.466 |
|
| 2011 |
Liu P, Krische MJ, Houk KN. Mechanism and origins of regio- and enantioselectivities in RhI-catalyzed hydrogenative couplings of 1,3-diynes and activated carbonyl partners: intervention of a cumulene intermediate. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 4021-9. PMID 21365696 DOI: 10.1002/Chem.201002741 |
0.486 |
|
| 2011 |
Rössle M, Del Valle DJ, Krische MJ. Synthesis of the cytotrienin A core via metal catalyzed C-C coupling. Organic Letters. 13: 1482-5. PMID 21323372 DOI: 10.1021/Ol200160P |
0.521 |
|
| 2011 |
Zbieg JR, McInturff EL, Leung JC, Krische MJ. Amplification of anti-diastereoselectivity via Curtin-Hammett effects in ruthenium-catalyzed hydrohydroxyalkylation of 1,1-disubstituted allenes: diastereoselective formation of all-carbon quaternary centers. Journal of the American Chemical Society. 133: 1141-4. PMID 21175178 DOI: 10.1021/Ja1104156 |
0.429 |
|
| 2011 |
Hassan A, Townsend IA, Krische MJ. Iridium-Catalyzed Asymmetric Allylations Synfacts. 2011: 1206-1206. DOI: 10.1055/S-0031-1289214 |
0.497 |
|
| 2011 |
Gao X, Han H, Krische MJ. Iridium-Catalyzed Asymmetric Double Crotylation of 1,3-Diols Synfacts. 2011: 1086-1086. DOI: 10.1055/S-0030-1261114 |
0.489 |
|
| 2011 |
Hassan A, Zbieg JR, Krische MJ. Ir-Catalyzed Enantioselective Vinylogous Reformatsky-TypeAldol Reaction Synfacts. 2011: 741-741. DOI: 10.1055/S-0030-1260661 |
0.376 |
|
| 2011 |
Gao X, Zhang YJ, Krische MJ. Iridium-Catalyzed anti-Diastereo-and Enantioselective Carbonyl Allylation Synfacts. 2011: 740-740. DOI: 10.1055/S-0030-1260639 |
0.411 |
|
| 2011 |
Krische M, Han S, Hassan A, Ku I. Total Synthesis of (+)-Roxaticin Synfacts. 2011: 0121-0121. DOI: 10.1055/S-0030-1259215 |
0.326 |
|
| 2010 |
Zbieg JR, Fukuzumi T, Krische MJ. Iridium Catalyzed Hydro-hydroxyalkylation of Butadiene: Carbonyl Crotylation. Advanced Synthesis & Catalysis. 352: 2416-2420. PMID 21165157 DOI: 10.1002/Adsc.201000599 |
0.535 |
|
| 2010 |
Han SB, Hassan A, Kim IS, Krische MJ. Total synthesis of (+)-roxaticin via C-C bond forming transfer hydrogenation: a departure from stoichiometric chiral reagents, auxiliaries, and premetalated nucleophiles in polyketide construction. Journal of the American Chemical Society. 132: 15559-61. PMID 20961111 DOI: 10.1021/Ja1082798 |
0.509 |
|
| 2010 |
Han SB, Gao X, Krische MJ. Iridium-catalyzed anti-diastereo- and enantioselective carbonyl (trimethylsilyl)allylation from the alcohol or aldehyde oxidation level. Journal of the American Chemical Society. 132: 9153-6. PMID 20540509 DOI: 10.1021/Ja103299F |
0.542 |
|
| 2010 |
Han H, Krische MJ. Direct ruthenium-catalyzed C-C coupling of ethanol: diene hydro-hydroxyethylation to form all-carbon quaternary centers. Organic Letters. 12: 2844-6. PMID 20491487 DOI: 10.1021/Ol101077V |
0.474 |
|
| 2010 |
Zbieg JR, McInturff EL, Krische MJ. Allenamide hydro-hydroxyalkylation: 1,2-amino alcohols via ruthenium-catalyzed carbonyl anti-aminoallylation. Organic Letters. 12: 2514-6. PMID 20459077 DOI: 10.1021/Ol1007235 |
0.484 |
|
| 2010 |
Zhang YJ, Yang JH, Kim SH, Krische MJ. anti-Diastereo- and enantioselective carbonyl (hydroxymethyl)allylation from the alcohol or aldehyde oxidation level: allyl carbonates as allylmetal surrogates. Journal of the American Chemical Society. 132: 4562-3. PMID 20225853 DOI: 10.1021/Ja100949E |
0.457 |
|
| 2010 |
Krische MJ. Cross-metathesis-based approaches to heteroaromatics: combining catalysts for furan formation. Proceedings of the National Academy of Sciences of the United States of America. 107: 3279-80. PMID 20167802 DOI: 10.1073/Pnas.1000313107 |
0.447 |
|
| 2010 |
Bechem B, Patman RL, Hashmi AS, Krische MJ. Enantioselective carbonyl allylation, crotylation, and tert-prenylation of furan methanols and furfurals via iridium-catalyzed transfer hydrogenation. The Journal of Organic Chemistry. 75: 1795-8. PMID 20131774 DOI: 10.1021/Jo902697G |
0.834 |
|
| 2010 |
Han SB, Han H, Krische MJ. Diastereo- and enantioselective anti-alkoxyallylation employing allylic gem-dicarboxylates as allyl donors via iridium-catalyzed transfer hydrogenation. Journal of the American Chemical Society. 132: 1760-1. PMID 20099821 DOI: 10.1021/Ja9097675 |
0.488 |
|
| 2010 |
Krische M, Han S, Gao X. anti-Diastereo- and Enantioselective Carbonyl (Trimethylsilyl)allylation Synfacts. 2010: 1273-1273. DOI: 10.1055/S-0030-1258791 |
0.447 |
|
| 2010 |
Zhang YJ, Yang JH, Kim SH, Krische MJ. Iridium-Catalyzed Enantioselective Carbonyl (Hydroxymethyl)allylation Synfacts. 2010: 801-801. DOI: 10.1055/S-0029-1220031 |
0.506 |
|
| 2010 |
Bechem B, Patman RL, Hashmi ASK, Krische MJ. Asymmetric Allylation, Crotylation, and tert-Prenylationof Furan Methanols and Furfurals Synfacts. 2010: 669-669. DOI: 10.1055/S-0029-1219902 |
0.472 |
|
| 2010 |
Han SB, Han H, Krische MJ. Iridium-Catalyzed Asymmetric Alkoxy-allylation of Aldehydes Synfacts. 2010: 571-571. DOI: 10.1055/S-0029-1219696 |
0.503 |
|
| 2010 |
Han SB, Kim IS, Han H, Krische MJ. Erratum: Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1,1-Dimethylallene as the prenyl donor (Journal of the American Chemical Society (2009) 131 (6916-6917)) Journal of the American Chemical Society. 132. DOI: 10.1021/Ja105736A |
0.334 |
|
| 2010 |
Bower JF, Krische MJ. ChemInform Abstract: Hydrogenation for C-C Bond Formation Cheminform. 41: no-no. DOI: 10.1002/chin.201024212 |
0.317 |
|
| 2010 |
Baik T, Luis AL, Wang L, Krische MJ. ChemInform Abstract: A Diastereoselective Metal-Catalyzed [2 + 2] Cycloaddition of Bis-enones. Cheminform. 32: no-no. DOI: 10.1002/chin.200143029 |
0.644 |
|
| 2010 |
Trost BM, Haffner CD, Jebaratnam DJ, Krische MJ, Thomas AP. ChemInform Abstract: The Palladium-Catalyzed Enyne Cycloisomerization Reaction in a General Approach to the Asymmetric Syntheses of the Picrotoxane Sesquiterpenes. Part 1. First-Generation Total Synthesis of Corianin (V) and Formal Syntheses of Picrotoxin Cheminform. 30: no-no. DOI: 10.1002/chin.199942110 |
0.513 |
|
| 2010 |
Trost B, Krische MJ. ChemInform Abstract: Palladium-Catalyzed Enyne Cycloisomerization Reaction in an Asymmetric Approach to the Picrotoxane Sesquiterpenes. Part 2. Second-Generation Total Syntheses of Corianin, Picrotoxinin, Picrotin, and Methyl Picrotoxate. Cheminform. 30: no-no. DOI: 10.1002/chin.199942109 |
0.509 |
|
| 2010 |
KRISCHE MJ, TROST BM. ChemInform Abstract: Transformations of the Picrotoxanes: The Synthesis of Corianin and Structural Analogues from Picrotoxinin. Cheminform. 29: no-no. DOI: 10.1002/chin.199840206 |
0.416 |
|
| 2010 |
KRISCHE MJ, TROST BM. ChemInform Abstract: Total Synthesis of Methyl Picrotoxate via the Palladium Catalyzed Enyne Cycloisomerization Reaction. Cheminform. 29: no-no. DOI: 10.1002/chin.199829224 |
0.511 |
|
| 2010 |
TROST BM, KRISCHE MJ. ChemInform Abstract: Transition Metal Catalyzed Cycloisomerizations Cheminform. 29: no-no. DOI: 10.1002/chin.199817285 |
0.421 |
|
| 2010 |
TROST BM, KRISCHE MJ, RADINOV R, ZANONI G. ChemInform Abstract: Asymmetric Induction in Allylic Alkylation via Enantiotopic Facial Discrimination. Cheminform. 27: no-no. DOI: 10.1002/chin.199641026 |
0.493 |
|
| 2010 |
TROST BM, KRISCHE MJ. ChemInform Abstract: General Strategy for the Asymmetric Synthesis of the Picrotoxanes. Cheminform. 27: no-no. DOI: 10.1002/chin.199618179 |
0.477 |
|
| 2010 |
Skucas E, Zbieg J, Krische M. Anti-Aminoallylation of aldehydes via ruthenium-catalyzed transfer hydrogenative coupling of sulfonamide allenes: 1,2-aminoalcohols Chemtracts. 23: 191-194. |
0.337 |
|
| 2009 |
Williams VM, Leung JC, Patman RL, Krische MJ. Hydroacylation of 2-Butyne from the Alcohol or Aldehyde Oxidation Level via Ruthenium Catalyzed C-C Bond Forming Transfer Hydrogenation. Tetrahedron. 65: 5024-5029. PMID 20613891 DOI: 10.1016/J.Tet.2009.03.068 |
0.823 |
|
| 2009 |
Han SB, Kim IS, Krische MJ. Enantioselective iridium-catalyzed carbonyl allylation from the alcohol oxidation level via transfer hydrogenation: minimizing pre-activation for synthetic efficiency. Chemical Communications (Cambridge, England). 7278-87. PMID 20024203 DOI: 10.1039/B917243M |
0.524 |
|
| 2009 |
Williams VM, Kong JR, Ko BJ, Mantri Y, Brodbelt JS, Baik MH, Krische MJ. ESI-MS, DFT, and synthetic studies on the H(2)-mediated coupling of acetylene: insertion of C=X bonds into rhodacyclopentadienes and Brønsted acid cocatalyzed hydrogenolysis of organorhodium intermediates. Journal of the American Chemical Society. 131: 16054-62. PMID 19845357 DOI: 10.1021/Ja906225N |
0.656 |
|
| 2009 |
Grant CD, Krische MJ. Protecting-group-free synthesis of 3-tert-prenylated oxindoles: contiguous all-carbon quaternary centers via tertiary neopentyl substitution. Organic Letters. 11: 4485-7. PMID 19764718 DOI: 10.1021/Ol9018562 |
0.44 |
|
| 2009 |
Zhang YJ, Skucas E, Krische MJ. Direct prenylation of aromatic and alpha,beta-unsaturated carboxamides via iridium-catalyzed C-H oxidative addition-allene insertion. Organic Letters. 11: 4248-50. PMID 19739691 DOI: 10.1021/Ol901759T |
0.329 |
|
| 2009 |
Itoh J, Han SB, Krische MJ. Enantioselective allylation, crotylation, and reverse prenylation of substituted isatins: iridium-catalyzed C-C bond-forming transfer hydrogenation. Angewandte Chemie (International Ed. in English). 48: 6313-6. PMID 19606435 DOI: 10.1002/Anie.200902328 |
0.58 |
|
| 2009 |
Smejkal T, Han H, Breit B, Krische MJ. All-carbon quaternary centers via ruthenium-catalyzed hydroxymethylation of 2-substituted butadienes mediated by formaldehyde: beyond hydroformylation. Journal of the American Chemical Society. 131: 10366-7. PMID 19594163 DOI: 10.1021/Ja904124B |
0.656 |
|
| 2009 |
Hassan A, Lu Y, Krische MJ. Elongation of 1,3-polyols via iterative catalyst-directed carbonyl allylation from the alcohol oxidation level. Organic Letters. 11: 3112-5. PMID 19586067 DOI: 10.1021/Ol901136W |
0.442 |
|
| 2009 |
Lu Y, Krische MJ. Concise synthesis of the bryostatin A-ring via consecutive C-C bond forming transfer hydrogenations. Organic Letters. 11: 3108-11. PMID 19586066 DOI: 10.1021/Ol901096D |
0.506 |
|
| 2009 |
Lu Y, Kim IS, Hassan A, Del Valle DJ, Krische MJ. 1,n-glycols as dialdehyde equivalents in iridium-catalyzed enantioselective carbonyl allylation and iterative two-directional assembly of 1,3-polyols. Angewandte Chemie (International Ed. in English). 48: 5018-21. PMID 19472247 DOI: 10.1002/Anie.200901648 |
0.464 |
|
| 2009 |
Han SB, Kim IS, Han H, Krische MJ. Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1,1-dimethylallene as the prenyl donor. Journal of the American Chemical Society. 131: 6916-7. PMID 19453190 DOI: 10.1021/Ja902437K |
0.523 |
|
| 2009 |
Jones RA, Krische MJ. Asymmetric total synthesis of the iridoid beta-glucoside (+)-geniposide via phosphine organocatalysis. Organic Letters. 11: 1849-51. PMID 19317433 DOI: 10.1021/Ol900360H |
0.393 |
|
| 2009 |
Skucas E, Zbieg JR, Krische MJ. anti-Aminoallylation of aldehydes via ruthenium-catalyzed transfer hydrogenative coupling of sulfonamido allenes: 1,2-aminoalcohols. Journal of the American Chemical Society. 131: 5054-5. PMID 19317402 DOI: 10.1021/Ja900827P |
0.439 |
|
| 2009 |
Kim IS, Han SB, Krische MJ. anti-Diastereo- and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level employing a cyclometallated iridium catalyst: alpha-methyl allyl acetate as a surrogate to preformed crotylmetal reagents. Journal of the American Chemical Society. 131: 2514-20. PMID 19191498 DOI: 10.1021/Ja808857W |
0.533 |
|
| 2009 |
Patman RL, Chaulagain MR, Williams VM, Krische MJ. Direct vinylation of alcohols or aldehydes employing alkynes as vinyl donors: a ruthenium catalyzed C-C bond-forming transfer hydrogenation. Journal of the American Chemical Society. 131: 2066-7. PMID 19173651 DOI: 10.1021/Ja809456U |
0.821 |
|
| 2009 |
Bower JF, Kim IS, Patman RL, Krische MJ. Catalytic carbonyl addition through transfer hydrogenation: a departure from preformed organometallic reagents. Angewandte Chemie (International Ed. in English). 48: 34-46. PMID 19040235 DOI: 10.1002/Anie.200802938 |
0.831 |
|
| 2009 |
Lu Y, Kim IS, Hassan A, Valle DJD, Krische MJ. Iridium-Catalyzed Stereoselective Two-Directional Elongationof 1,3-Polyols Synfacts. 2009: 997-997. DOI: 10.1055/S-0029-1217666 |
0.433 |
|
| 2009 |
Skucas E, Zbieg JR, Krische MJ. Diastereoselective Ruthenium-Catalyzed Aminoallylation Synfacts. 2009: 631-631. DOI: 10.1055/S-0029-1217150 |
0.477 |
|
| 2009 |
Patman RL, Chaulagain MR, Williams VM, Krische MJ. Ruthenium-Catalyzed Direct Vinylation of Alcohols and Aldehydes Synfacts. 2009: 550-550. DOI: 10.1055/S-0028-1088185 |
0.378 |
|
| 2009 |
Lu Y, Krische MJ. Concise synthesis of the bryostatin A-ring via consecutive C-C bond forming transfer hydrogenations (Organic Letters (2009) 11 (3109)) Organic Letters. 11: 5362. DOI: 10.1021/Ol9023634 |
0.465 |
|
| 2009 |
Shibahara F, Bower JF, Krische MJ. ChemInform Abstract: Diene Hydroacylation from the Alcohol or Aldehyde Oxidation Level via Ruthenium-Catalyzed C-C Bond-Forming Transfer Hydrogenation: Synthesis of β,γ-Unsaturated Ketones. Cheminform. 40. DOI: 10.1002/chin.200909078 |
0.417 |
|
| 2009 |
Liechti KM, Wakamatsu M, Doynov B, Ngai MY, Krische MJ. Fracture between self-assembled monolayers Iccm International Conferences On Composite Materials. |
0.686 |
|
| 2008 |
Patman RL, Bower JF, Kim IS, Krische MJ. Formation of C-C Bonds via Catalytic Hydrogenation and Transfer Hydrogenation: Vinylation, Allylation, and Enolate Addition of Carbonyl Compounds and Imines. Aldrichimica Acta. 41: 95-104. PMID 22403445 DOI: 10.1002/9781118354520.ch16 |
0.83 |
|
| 2008 |
Shibahara F, Krische MJ. Formation of C-C Bonds via Ruthenium Catalyzed Transfer Hydrogenation: Carbonyl Addition from the Alcohol or Aldehyde Oxidation Level. Chemistry Letters. 37: 1102-1107. PMID 21927534 DOI: 10.1246/Cl.2008.1102 |
0.525 |
|
| 2008 |
Han SB, Hassan A, Krische MJ. Diastereo- and Enantioselective Reductive Aldol Addition of Vinyl Ketones via Catalytic Hydrogenation. Synthesis. 2008: 2669-2679. PMID 21866204 DOI: 10.1055/S-2008-1067220 |
0.51 |
|
| 2008 |
Komanduri V, Pedraza F, Krische MJ. Direct Copper-Free Domino Conjugate Addition-Cycloallylation using Organozinc Reagents. Advanced Synthesis & Catalysis. 350: 1569-1576. PMID 20454546 DOI: 10.1002/Adsc.200800242 |
0.392 |
|
| 2008 |
Webber P, Krische MJ. Concise stereocontrolled formal synthesis of (+/-)-quinine and total synthesis of (+/-)-7- hydroxyquinine via merged Morita-Baylis-Hillman-Tsuji-Trost cyclization. The Journal of Organic Chemistry. 73: 9379-87. PMID 18989927 DOI: 10.1021/Jo802165K |
0.8 |
|
| 2008 |
Kim IS, Ngai MY, Krische MJ. Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level via transfer hydrogenative coupling of allyl acetate: departure from chirally modified allyl metal reagents in carbonyl addition. Journal of the American Chemical Society. 130: 14891-9. PMID 18841896 DOI: 10.1021/Ja805722E |
0.83 |
|
| 2008 |
Shibahara F, Bower JF, Krische MJ. Diene hydroacylation from the alcohol or aldehyde oxidation level via ruthenium-catalyzed C-C bond-forming transfer hydrogenation: synthesis of beta,gamma-unsaturated ketones. Journal of the American Chemical Society. 130: 14120-2. PMID 18841895 DOI: 10.1021/Ja805356J |
0.716 |
|
| 2008 |
Komanduri V, Grant CD, Krische MJ. Branch-selective reductive coupling of 2-vinyl pyridines and imines via rhodium catalyzed C-C bond forming hydrogenation. Journal of the American Chemical Society. 130: 12592-3. PMID 18759388 DOI: 10.1021/Ja805056G |
0.523 |
|
| 2008 |
Han SB, Kong JR, Krische MJ. Catalyst-directed diastereoselectivity in hydrogenative couplings of acetylene to alpha-chiral aldehydes: formal synthesis of all eight L-hexoses. Organic Letters. 10: 4133-5. PMID 18729371 DOI: 10.1021/Ol8018874 |
0.659 |
|
| 2008 |
Ngai MY, Skucas E, Krische MJ. Ruthenium catalyzed C-C bond formation via transfer hydrogenation: branch-selective reductive coupling of allenes to paraformaldehyde and higher aldehydes. Organic Letters. 10: 2705-8. PMID 18533665 DOI: 10.1021/Ol800836V |
0.818 |
|
| 2008 |
Patman RL, Williams VM, Bower JF, Krische MJ. Carbonyl propargylation from the alcohol or aldehyde oxidation level employing 1,3-enynes as surrogates to preformed allenylmetal reagents: a ruthenium-catalyzed C-C bond-forming transfer hydrogenation. Angewandte Chemie (International Ed. in English). 47: 5220-3. PMID 18528831 DOI: 10.1002/Anie.200801359 |
0.859 |
|
| 2008 |
Shibahara F, Bower JF, Krische MJ. Ruthenium-catalyzed C-C bond forming transfer hydrogenation: carbonyl allylation from the alcohol or aldehyde oxidation level employing acyclic 1,3-dienes as surrogates to preformed allyl metal reagents. Journal of the American Chemical Society. 130: 6338-9. PMID 18444617 DOI: 10.1021/Ja801213X |
0.737 |
|
| 2008 |
Kim IS, Ngai MY, Krische MJ. Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level using allyl acetate as an allyl metal surrogate. Journal of the American Chemical Society. 130: 6340-1. PMID 18444616 DOI: 10.1021/Ja802001B |
0.822 |
|
| 2008 |
Bee C, Han SB, Hassan A, Iida H, Krische MJ. Diastereo- and enantioselective hydrogenative aldol coupling of vinyl ketones: design of effective monodentate TADDOL-like phosphonite ligands. Journal of the American Chemical Society. 130: 2746-7. PMID 18266373 DOI: 10.1021/Ja710862U |
0.497 |
|
| 2008 |
Bower JF, Patman RL, Krische MJ. Iridium-catalyzed C-C coupling via transfer hydrogenation: carbonyl addition from the alcohol or aldehyde oxidation level employing 1,3-cyclohexadiene. Organic Letters. 10: 1033-5. PMID 18254642 DOI: 10.1021/Ol800159W |
0.845 |
|
| 2008 |
Kim IS, Krische MJ. Iridium-catalyzed hydrocarboxylation of 1,1-dimethylallene: byproduct-free reverse prenylation of carboxylic acids. Organic Letters. 10: 513-5. PMID 18181640 DOI: 10.1021/Ol702914P |
0.431 |
|
| 2008 |
Kim IS, Ngai M-, Krische MJ. Enantioselective Iridium-Catalyzed Carbonyl Allylations withAllyl Acetate Synfacts. 2008: 957-957. DOI: 10.1055/S-2008-1078635 |
0.501 |
|
| 2008 |
Shibahara F, Bower JF, Krische MJ. Ru-Catalyzed Carbonyl Allylations from Alcohols or Aldehydes Synfacts. 2008: 831-831. DOI: 10.1055/S-2008-1077906 |
0.666 |
|
| 2008 |
Bower JF, Patman RL, Krische MJ. Iridium-Promoted C-C Coupling through Transfer Hydrogenation Synfacts. 2008: 505-505. DOI: 10.1055/S-2008-1072635 |
0.69 |
|
| 2008 |
Bee C, Han SB, Hassan A, Iida H, Krische MJ. Rhodium-Catalyzed Reductive Aldol Reaction of Vinyl Ketones Synfacts. 2008: 596-596. DOI: 10.1055/S-2008-1072618 |
0.406 |
|
| 2008 |
Bower JF, Skucas E, Patman RL, Krische MJ. Reverse Prenylation, Crotylation and Allylation of Alcohols and Aldehydes via Transfer Hydrogenation Synfacts. 2008: 293-293. DOI: 10.1055/S-2008-1042740 |
0.677 |
|
| 2008 |
Ngai M-, Barchuk A, Krische MJ. Iridium-Catalyzed Enantioselective Alkyne-Imine Reductive Coupling Synfacts. 2008: 159-159. DOI: 10.1055/S-2007-992487 |
0.452 |
|
| 2008 |
Komanduri V, Grant CD, Krische MJ. Rhodium-Catalyzed Reductive Coupling of 2-VinylPyridines and Imines Synfacts. 2008: 1294-1294. DOI: 10.1055/S-0028-1087315 |
0.414 |
|
| 2008 |
Krische M, Han S, Kong J. Coupling of Acetylene and Aldehydes Applied tol-Hexoses Synthesis Synfacts. 2008: 1197-1197. DOI: 10.1055/S-0028-108433 |
0.609 |
|
| 2008 |
Hong Y, Cho C, Skucas E, Krische MJ. ChemInform Abstract: Enantioselective Reductive Coupling of 1,3-Enynes to Glyoxalates Mediated by Hydrogen: Asymmetric Synthesis of β,γ-Unsaturated α-Hydroxy Esters. Cheminform. 39. DOI: 10.1002/chin.200804076 |
0.311 |
|
| 2008 |
Bower J, Kim I, Patman R, Krische M. Katalytische Carbonyladdition durch Transferhydrierung: weg von vorab gebildeten Organometallreagentien Angewandte Chemie. 121: 36-48. DOI: 10.1002/Ange.200802938 |
0.786 |
|
| 2008 |
Garner SA, Han SB, Krische MJ. Metal-Catalyzed Reductive Aldol Coupling Modern Reduction Methods. 387-417. DOI: 10.1002/9783527622115.ch16 |
0.757 |
|
| 2007 |
Bower JF, Skucas E, Patman RL, Krische MJ. Catalytic C-C coupling via transfer hydrogenation: reverse prenylation, crotylation, and allylation from the alcohol or aldehyde oxidation level. Journal of the American Chemical Society. 129: 15134-5. PMID 18020342 DOI: 10.1021/Ja077389B |
0.824 |
|
| 2007 |
Ngai MY, Barchuk A, Krische MJ. Enantioselective iridium-catalyzed imine vinylation: optically enriched allylic amines via alkyne-imine reductive coupling mediated by hydrogen. Journal of the American Chemical Society. 129: 12644-5. PMID 17914825 DOI: 10.1021/Ja075438E |
0.824 |
|
| 2007 |
Skucas E, Bower JF, Krische MJ. Carbonyl allylation in the absence of preformed allyl metal reagents: reverse prenylation via iridium-catalyzed hydrogenative coupling of dimethylallene. Journal of the American Chemical Society. 129: 12678-9. PMID 17900123 DOI: 10.1021/Ja075971U |
0.732 |
|
| 2007 |
Skucas E, Ngai MY, Komanduri V, Krische MJ. Enantiomerically enriched allylic alcohols and allylic amines via C-C bond-forming hydrogenation: asymmetric carbonyl and imine vinylation. Accounts of Chemical Research. 40: 1394-401. PMID 17784728 DOI: 10.1021/Ar7001123 |
0.826 |
|
| 2007 |
Hong YT, Cho CW, Skucas E, Krische MJ. Enantioselective reductive coupling of 1,3-enynes to glyoxalates mediated by hydrogen: asymmetric synthesis of beta,gamma-unsaturated alpha-hydroxy esters. Organic Letters. 9: 3745-8. PMID 17705502 DOI: 10.1021/Ol7015548 |
0.44 |
|
| 2007 |
Garner SA, Krische MJ. Rhodium-catalyzed reductive mannich coupling of vinyl ketones to N-sulfonylimines mediated by hydrogen. The Journal of Organic Chemistry. 72: 5843-6. PMID 17583961 DOI: 10.1021/Jo070779W |
0.803 |
|
| 2007 |
Barchuk A, Ngai MY, Krische MJ. Allylic amines via iridium-catalyzed C-C bond forming hydrogenation: imine vinylation in the absence of stoichiometric byproducts or metallic reagents. Journal of the American Chemical Society. 129: 8432-3. PMID 17571894 DOI: 10.1021/Ja073018J |
0.805 |
|
| 2007 |
Skucas E, Kong JR, Krische MJ. Enantioselective reductive coupling of acetylene to N-arylsulfonyl imines via rhodium catalyzed C-C bond-forming hydrogenation: (Z)-dienyl allylic amines. Journal of the American Chemical Society. 129: 7242-3. PMID 17511459 DOI: 10.1021/Ja0715896 |
0.689 |
|
| 2007 |
Ngai MY, Kong JR, Krische MJ. Hydrogen-mediated C-C bond formation: a broad new concept in catalytic C-C coupling. The Journal of Organic Chemistry. 72: 1063-72. PMID 17288361 DOI: 10.1021/Jo061895M |
0.821 |
|
| 2007 |
Ngai MY, Barchuk A, Krische MJ. Iridium-catalyzed C-C bond forming hydrogenation: direct regioselective reductive coupling of alkyl-substituted alkynes to activated ketones. Journal of the American Chemical Society. 129: 280-1. PMID 17212400 DOI: 10.1021/Ja0670815 |
0.821 |
|
| 2007 |
Jong UR, Jones RA, Krische MJ. Catalytic enantioselective reductive cyclization of acetylenic aldehydes via hydrogenation Synthesis. 3427-3430. DOI: 10.1055/S-2007-983829 |
0.536 |
|
| 2007 |
Barchuk A, Ngai MY, Krische MJ. Allylic Amines via Iridium-Catalyzed C-C Bond-Forming Hydrogenation Synfacts. 2007: 976-976. DOI: 10.1055/S-2007-968827 |
0.476 |
|
| 2007 |
Krische M, Komanduri V. Reductive Coupling via Rhodium-Catalyzed Asymmetric Hydrogenation Synfacts. 2007: 0300-0300. DOI: 10.1055/s-2007-968243 |
0.377 |
|
| 2007 |
Cho CW, Skucas E, Krische MJ. Contrasteric regiocontrol in rhodium-catalyzed hydrogenative couplings of nonsymmetric 1,3-diynes to ethyl glyoxalate Organometallics. 26: 3860-3867. DOI: 10.1021/Om7003089 |
0.476 |
|
| 2007 |
Cho CW, Krische MJ. Erratum: α-hydroxy esters via enantioselective hydrogen-mediated C-C coupling: Regiocontrolled reactions of silyl-substituted 1,3-diynes (Organic Letters (2006) 8) Organic Letters. 9. DOI: 10.1021/Ol070060A |
0.5 |
|
| 2007 |
Huddleston RR, Jang HY, Krische MJ. First Catalytic Reductive Coupling of 1,3-Diynes to Carbonyl Partners: A New Regio- and Enantioselective C−C Bond Forming Hydrogenation [J. Am. Chem. Soc. 2003, 125, 11488−11489]. Journal of the American Chemical Society. 129: 2194-2194. DOI: 10.1021/Ja070167T |
0.463 |
|
| 2007 |
Krische MJ, Sun Y. Hydrogenation and Transfer Hydrogenation Accounts of Chemical Research. 40: 1237-1237. DOI: 10.1021/Ar700250E |
0.36 |
|
| 2007 |
Iida H, Krische MJ. Catalytic reductive coupling of alkenes and alkynes to carbonyl compounds and imines mediated by hydrogen Topics in Current Chemistry. 279: 77-104. DOI: 10.1007/128_2007_122 |
0.346 |
|
| 2007 |
Krische MJ, Jang HY. Metal-catalyzed reductive carbocyclization (C=C, C=C, C=O bonds) Comprehensive Organometallic Chemistry Iii. 10: 493-536. |
0.525 |
|
| 2006 |
Jung CK, Krische MJ. Asymmetric induction in hydrogen-mediated reductive aldol additions to alpha-amino aldehydes catalyzed by rhodium: selective formation of syn-stereotriads directed by intramolecular hydrogen-bonding. Journal of the American Chemical Society. 128: 17051-6. PMID 17177457 DOI: 10.1021/Ja066198Q |
0.691 |
|
| 2006 |
Komanduri V, Krische MJ. Enantioselective reductive coupling of 1,3-enynes to heterocyclic aromatic aldehydes and ketones via rhodium-catalyzed asymmetric hydrogenation: mechanistic insight into the role of Brønsted acid additives. Journal of the American Chemical Society. 128: 16448-9. PMID 17177363 DOI: 10.1021/Ja0673027 |
0.552 |
|
| 2006 |
Kong JR, Krische MJ. Catalytic carbonyl Z-dienylation via multicomponent reductive coupling of acetylene to aldehydes and alpha-ketoesters mediated by hydrogen: Carbonyl insertion into cationic rhodacyclopentadienes. Journal of the American Chemical Society. 128: 16040-1. PMID 17165749 DOI: 10.1021/Ja0664786 |
0.677 |
|
| 2006 |
Han SB, Krische MJ. Reductive aldol coupling of divinyl ketones via rhodium-catalyzed hydrogenation: syn-diastereoselective construction of beta-hydroxyenones. Organic Letters. 8: 5657-60. PMID 17107096 DOI: 10.1021/Ol0624023 |
0.452 |
|
| 2006 |
Park H, Cho CW, Krische MJ. Phosphine-catalyzed allylic substitution of Morita-Baylis-Hillman acetates: synthesis of N-protected beta-aminophosphonic acid esters. The Journal of Organic Chemistry. 71: 7892-4. PMID 16995707 DOI: 10.1021/Jo061218S |
0.353 |
|
| 2006 |
Hong YT, Barchuk A, Krische MJ. Branch-selective intermolecular hydroacylation: hydrogen-mediated coupling of anhydrides to styrenes and activated olefins. Angewandte Chemie (International Ed. in English). 45: 6885-8. PMID 16991162 DOI: 10.1002/Anie.200602377 |
0.422 |
|
| 2006 |
Rhee JU, Krische MJ. Highly enantioselective reductive cyclization of acetylenic aldehydes via rhodium catalyzed asymmetric hydrogenation. Journal of the American Chemical Society. 128: 10674-5. PMID 16910650 DOI: 10.1021/Ja0637954 |
0.524 |
|
| 2006 |
Cho CW, Krische MJ. Alpha-hydroxy esters via enantioselective hydrogen-mediated C-C coupling: regiocontrolled reactions of silyl-substituted 1,3-diynes. Organic Letters. 8: 3873-6. PMID 16898839 DOI: 10.1021/Ol061485K |
0.524 |
|
| 2006 |
Cho CW, Krische MJ. Enantioselective reductive coupling of alkynes and α-keto aldehydes via rhodium-catalyzed hydrogenation: An approach to bryostatin substructures Organic Letters. 8: 891-894. PMID 16494467 DOI: 10.1021/Ol052976S |
0.468 |
|
| 2006 |
Jung CK, Garner SA, Krische MJ. Hydrogen-mediated aldol reductive coupling of vinyl ketones catalyzed by rhodium: high syn-selectivity through the effect of tri-2-furylphosphine. Organic Letters. 8: 519-22. PMID 16435874 DOI: 10.1021/Ol052859X |
0.845 |
|
| 2006 |
Kong JR, Ngai MY, Krische MJ. Highly enantioselective direct reductive coupling of conjugated alkynes and alpha-ketoesters via rhodium-catalyzed asymmetric hydrogenation. Journal of the American Chemical Society. 128: 718-9. PMID 16417351 DOI: 10.1021/Ja056474L |
0.843 |
|
| 2006 |
Rhee JU, Krische MJ. Alkynes as synthetic equivalents to stabilized Wittig reagents: intra- and intermolecular carbonyl olefinations catalyzed by Ag(I), BF3, and HBF4. Organic Letters. 7: 2493-5. PMID 15932231 DOI: 10.1021/ol050838x |
0.359 |
|
| 2006 |
Krische M, Rhee J. Reductive Cyclization of Acetylenic Aldehydes via Hydrogenation Synfacts. 2006: 1137-1137. DOI: 10.1055/s-2006-949443 |
0.349 |
|
| 2006 |
Krische M, Cho C. Reductive Coupling of Alkynes and α-Keto Aldehydes Synfacts. 2006: 0685-0685. DOI: 10.1055/S-2006-941812 |
0.361 |
|
| 2006 |
Krische M, Jung C, Garner S. Hydrogen-Mediated Aldol Reductive Coupling of Vinyl Ketones Synfacts. 2006: 0460-0460. DOI: 10.1055/S-2006-934441 |
0.828 |
|
| 2006 |
Kong J, Ngai M, Krische MJ. Enantioselective Direct Reductive Coupling of Conjugated Alkynes and α-Ketoesters Synfacts. 2006: 359-359. DOI: 10.1055/S-2006-934337 |
0.772 |
|
| 2006 |
Koech PK, Krische MJ. Enantioselective total and formal syntheses of paroxetine (PAXIL) via phosphine-catalyzed enone α-arylation using arylbismuth(V) reagents: a regiochemical complement to Heck arylation Tetrahedron. 62: 10594-10602. DOI: 10.1016/J.Tet.2006.05.092 |
0.693 |
|
| 2006 |
Balaban TS, Eichhöfer A, Krische MJ, Lehn JM. Hierarchic supramolecular interactions within assemblies in solution and in the crystal of 2,3,6,7-tetrasubstituted 5,5′-(anthracene-9,10-diyl) bis[pyrimidin-2-amines] Helvetica Chimica Acta. 89: 333-351. DOI: 10.1002/Hlca.200690037 |
0.485 |
|
| 2005 |
Gong H, Krische MJ. Hydrogen-bond-mediated self-assembly of aminopyrazolones: macrocyclic quartets-single and stacked one-dimensional motifs. Angewandte Chemie (International Ed. in English). 44: 7069-71. PMID 16211644 DOI: 10.1002/Anie.200502539 |
0.54 |
|
| 2005 |
Kong JR, Cho CW, Krische MJ. Hydrogen-mediated reductive coupling of conjugated alkynes with ethyl (N-Sulfinyl)iminoacetates: synthesis of unnatural alpha-amino acids via rhodium-catalyzed C-C bond forming hydrogenation. Journal of the American Chemical Society. 127: 11269-76. PMID 16089454 DOI: 10.1021/Ja051104I |
0.669 |
|
| 2005 |
Jang HY, Hughes FW, Gong H, Zhang J, Brodbelt JS, Krische MJ. Enantioselective reductive cyclization of 1,6-enynes via rhodium-catalyzed asymmetric hydrogenation: C-C bond formation precedes hydrogen activation. Journal of the American Chemical Society. 127: 6174-5. PMID 15853314 DOI: 10.1021/Ja042645V |
0.754 |
|
| 2005 |
Gong H, Krische MJ. Duplex molecular strands based on the 3,6-diaminopyridazine hydrogen bonding motif: amplifying small-molecule self-assembly preferences through preorganization and iterative arrangement of binding residues. Journal of the American Chemical Society. 127: 1719-25. PMID 15701006 DOI: 10.1021/Ja044566P |
0.523 |
|
| 2005 |
Krische M, Kong J, Cho C. Synthesis of Unnatural Amino Acids via Reductive C-C Bond Forming Hydrogenation Synfacts. 2006: 0049-0049. DOI: 10.1055/S-2005-921671 |
0.44 |
|
| 2005 |
Rhee JU, Krische MJ. Alkynes as synthetic equivalents to stabilized wittig reagents: Intra- and intermolecular carbonyl olefinations catalyzed by Ag(I), BF3, and HBF4 Organic Letters. 7: 2493-2495. DOI: 10.1021/Ol050838X |
0.445 |
|
| 2005 |
Kong J, Cho C, Krische MJ. Hydrogen-Mediated Reductive Coupling of Conjugated Alkynes with Ethyl (N-Sulfinyl)iminoacetates: Synthesis of Unnatural α-Amino Acids via Rhodium-Catalyzed C−C Bond Forming Hydrogenation [J. Am. Chem. Soc.2005,127, 11269−11276]. Journal of the American Chemical Society. 127: 16338-16338. DOI: 10.1021/Ja059919E |
0.451 |
|
| 2005 |
Bocknack BM, Wang LC, Hughes FW, Krische MJ. Chiral β-diketonate ligands of 'pseudo planar chiral' topology: Enantioselective synthesis and transition metal complexation Tetrahedron. 61: 6266-6275. DOI: 10.1016/J.Tet.2005.03.118 |
0.783 |
|
| 2005 |
Krische MJ. Asymmetric Organocatalysis. From Biomimetic Concepts to Applications in Asymmetric Synthesis. By Albrecht Berkessel and Harald Gröger. Angewandte Chemie International Edition. 44: 4285-4286. DOI: 10.1002/Anie.200585291 |
0.351 |
|
| 2004 |
Cho CW, Krische MJ. Regio- and stereoselective construction of γ-butenolides through phosphine-catalyzed substitution of Morita-Baylis-Hillman acetates: An organocatalytic allylic alkylation Angewandte Chemie - International Edition. 43: 6689-6691. PMID 15593162 DOI: 10.1002/Anie.200461381 |
0.454 |
|
| 2004 |
Yang J, Cauble DF, Berro AJ, Bauld NL, Krische MJ. Anion radical [2 + 2] cycloaddition as a mechanistic probe: stoichiometry- and concentration-dependent partitioning of electron-transfer and alkylation pathways in the reaction of the Gilman reagent Me2CuLi.LiI with bis(enones). The Journal of Organic Chemistry. 69: 7979-84. PMID 15527279 DOI: 10.1021/Jo048499T |
0.801 |
|
| 2004 |
Jang HY, Krische MJ. Catalytic C-C bond formation via capture of hydrogenation intermediates. Accounts of Chemical Research. 37: 653-61. PMID 15379581 DOI: 10.1021/Ar020108E |
0.647 |
|
| 2004 |
Jang HY, Krische MJ. Rhodium-catalyzed reductive cyclization of 1,6-diynes and 1,6-enynes mediated by hydrogen: catalytic C-C bond formation via capture of hydrogenation intermediates. Journal of the American Chemical Society. 126: 7875-80. PMID 15212535 DOI: 10.1021/Ja048498I |
0.627 |
|
| 2004 |
Koech PK, Krische MJ. Phosphine catalyzed alpha-arylation of enones and enals using hypervalent bismuth reagents: regiospecific enolate arylation via nucleophilic catalysis. Journal of the American Chemical Society. 126: 5350-1. PMID 15113193 DOI: 10.1021/Ja048987I |
0.689 |
|
| 2004 |
Jang HY, Huddleston RR, Krische MJ. Hydrogen-mediated C-C bond formation: catalytic regio- and stereoselective reductive condensation of alpha-keto aldehydes and 1,3-enynes. Journal of the American Chemical Society. 126: 4664-8. PMID 15070383 DOI: 10.1021/Ja0316566 |
0.674 |
|
| 2004 |
Agapiou K, Cauble DF, Krische MJ. Copper-catalyzed tandem conjugate addition-electrophilic trapping: ketones, esters, and nitriles as terminal electrophiles. Journal of the American Chemical Society. 126: 4528-9. PMID 15070365 DOI: 10.1021/Ja030603L |
0.808 |
|
| 2004 |
Cho CW, Kong JR, Krische MJ. Phosphine-catalyzed regiospecific allylic amination and dynamic kinetic resolution of Morita-Baylis-Hillman acetates. Organic Letters. 6: 1337-9. PMID 15070331 DOI: 10.1021/Ol049600J |
0.632 |
|
| 2004 |
Jung CK, Wang JC, Krische MJ. Phosphine-mediated reductive condensation of gamma-acyloxy butynoates: a diversity oriented strategy for the construction of substituted furans. Journal of the American Chemical Society. 126: 4118-9. PMID 15053596 DOI: 10.1021/Ja049377L |
0.624 |
|
| 2004 |
Bocknack BM, Wang LC, Krische MJ. Desymmetrization of enone-diones via rhodium-catalyzed diastereo- and enantioselective tandem conjugate addition-aldol cyclization. Proceedings of the National Academy of Sciences of the United States of America. 101: 5421-4. PMID 15024093 DOI: 10.1073/Pnas.0307120101 |
0.829 |
|
| 2004 |
Koech PK, Krische MJ. Catalytic addition of metallo-aldehyde enolates to ketones: a new C-C bond-forming hydrogenation. Organic Letters. 6: 691-4. PMID 14986951 DOI: 10.1021/Ol030136C |
0.768 |
|
| 2004 |
Marriner GA, Garner SA, Jang HY, Krische MJ. Metallo-aldehyde enolates via enal hydrogenation: catalytic cross aldolization with glyoxal partners as applied to the synthesis of 3,5-disubstituted pyridazines. The Journal of Organic Chemistry. 69: 1380-2. PMID 14961698 DOI: 10.1021/Jo030310A |
0.829 |
|
| 2004 |
Yang J, Felton GA, Bauld NL, Krische MJ. Chemically induced anion radical cycloadditions: intramolecular cyclobutanation of bis(enones) via homogeneous electron transfer. Journal of the American Chemical Society. 126: 1634-5. PMID 14871085 DOI: 10.1021/Ja030543J |
0.343 |
|
| 2004 |
Luis AL, Krische MJ. Nucleophilic catalysis via phosphine conjugate addition: Vinyl sulfones as reacting partners in catalytic cross-Michael cycloisomerization Synthesis. 2579-2585. DOI: 10.1055/S-2004-831191 |
0.71 |
|
| 2004 |
Jang HY, Krische MJ. Catalytic hydrogen-mediated cross-coupling of enones and carbonyl compounds: Aldol condensation by hydrogenation European Journal of Organic Chemistry. 3953-3958. DOI: 10.1002/Ejoc.200400270 |
0.632 |
|
| 2003 |
Wang JC, Krische MJ. Intramolecular Organocatalytic [3+2] Dipolar Cycloaddition: Stereospecific Cycloaddition and the Total Synthesis of (±)-Hirsutene Angewandte Chemie - International Edition. 42: 5855-5857. PMID 14673917 DOI: 10.1002/Anie.200352218 |
0.3 |
|
| 2003 |
Huddleston RR, Jang HY, Krische MJ. First catalytic reductive coupling of 1,3-diynes to carbonyl partners: a new regio- and enantioselective C-C bond forming hydrogenation. Journal of the American Chemical Society. 125: 11488-9. PMID 13129338 DOI: 10.1021/Ja030415V |
0.68 |
|
| 2003 |
Jang HY, Huddleston RR, Krische MJ. A New catalytic C[bond]C bond-forming hydrogenation: reductive coupling of dienes and glyoxals under catalytic hydrogenation conditions. Angewandte Chemie (International Ed. in English). 42: 4074-7. PMID 12973774 DOI: 10.1002/Anie.200351986 |
0.641 |
|
| 2003 |
Jellerichs BG, Kong JR, Krische MJ. Catalytic enone cycloallylation via concomitant activation of latent nucleophilic and electrophilic partners: merging organic and transition metal catalysis. Journal of the American Chemical Society. 125: 7758-9. PMID 12822967 DOI: 10.1021/Ja0301469 |
0.591 |
|
| 2003 |
Agapiou K, Krische MJ. Catalytic crossed Michael cycloisomerization of thioenoates: total synthesis of (+/-)-ricciocarpin A. Organic Letters. 5: 1737-40. PMID 12735765 DOI: 10.1021/Ol030035E |
0.425 |
|
| 2003 |
Huddleston RR, Krische MJ. Enolate generation under hydrogenation conditions: catalytic aldol cycloreduction of keto-enones. Organic Letters. 5: 1143-6. PMID 12659594 DOI: 10.1021/Ol0300219 |
0.513 |
|
| 2003 |
Wang JC, Ng SS, Krische MJ. Catalytic diastereoselective synthesis of diquinanes from acyclic precursors Journal of the American Chemical Society. 125: 3682-3683. PMID 12656582 DOI: 10.1021/Ja030022W |
0.383 |
|
| 2003 |
Cauble DF, Gipson JD, Krische MJ. Diastereo- and enantioselective catalytic carbometallative aldol cycloreduction: tandem conjugate addition-aldol cyclization. Journal of the American Chemical Society. 125: 1110-1. PMID 12553780 DOI: 10.1021/Ja0211095 |
0.83 |
|
| 2003 |
Cauble DF, Lynch V, Krische MJ. Studies on the enantioselective catalysis of photochemically promoted transformations: "sensitizing receptors" as chiral catalysts. The Journal of Organic Chemistry. 68: 15-21. PMID 12515455 DOI: 10.1021/Jo020630E |
0.798 |
|
| 2003 |
Huddleston RR, Cauble DF, Krische MJ. Borane-mediated aldol cycloreduction of monoenone monoketones: diastereoselective formation of quaternary centers. The Journal of Organic Chemistry. 68: 11-4. PMID 12515454 DOI: 10.1021/Jo020629F |
0.813 |
|
| 2003 |
Huddleston RR, Krische MJ. Enones as latent enolates in catalytic processes: Catalytic cycloreduction, cycloaddition and cycloisomerization Synlett. 12-21. DOI: 10.1055/S-2003-36213 |
0.388 |
|
| 2003 |
Jamison TF, Lubell WD, Dener JM, Krisché MJ, Rapoport H. 9‐Bromo‐9‐Phenylfluorene Organic Syntheses. 220-220. DOI: 10.1002/0471264180.Os071.28 |
0.512 |
|
| 2003 |
Jang HY, Huddleston RR, Krische MJ. Nucleophilic Activation of Enones via Homogeneous Catalytic Hydrogenation: Catalytic Reductive C-C Bond Formation Under Hydrogenation Conditions Chemtracts. 16: 554-559. |
0.591 |
|
| 2002 |
Jang HY, Huddleston RR, Krische MJ. Reductive generation of enolates from enones using elemental hydrogen: catalytic C-C bond formation under hydrogenative conditions. Journal of the American Chemical Society. 124: 15156-7. PMID 12487574 DOI: 10.1021/Ja021163L |
0.647 |
|
| 2002 |
Wang LC, Jang HY, Roh Y, Lynch V, Schultz AJ, Wang X, Krische MJ. Diastereoselective cycloreductions and cycloadditions catalyzed by Co(dpm)(2)-silane (dpm = 2,2,6,6-tetramethylheptane-3,5-dionate): mechanism and partitioning of hydrometallative versus anion radical pathways. Journal of the American Chemical Society. 124: 9448-53. PMID 12167039 DOI: 10.1021/Ja020223K |
0.629 |
|
| 2002 |
Trost BM, Krische MJ, Berl V, Grenzer EM. Chemo-, regio-, and enantioselective Pd-catalyzed allylic alkylation of indolocarbazole pro-aglycons. Organic Letters. 4: 2005-8. PMID 12049503 DOI: 10.1021/Ol020046S |
0.598 |
|
| 2002 |
Archer EA, Krische MJ. Duplex oligomers defined via covalent casting of a one-dimensional hydrogen-bonding motif. Journal of the American Chemical Society. 124: 5074-83. PMID 11982372 DOI: 10.1021/Ja012696H |
0.339 |
|
| 2002 |
Berl V, Schmutz M, Krische MJ, Khoury RG, Lehn JM. Supramolecular polymers generated from heterocomplementary monomers linked through multiple hydrogen-bonding arrays--formation, characterization, and properties. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 1227-44. PMID 11891911 DOI: 10.1002/1521-3765(20020301)8:5<1227::Aid-Chem1227>3.0.Co;2-0 |
0.474 |
|
| 2002 |
Wang LC, Luis AL, Agapiou K, Jang HY, Krische MJ. Organocatalytic Michael cycloisomerization of bis(enones): the intramolecular Rauhut-Currier reaction. Journal of the American Chemical Society. 124: 2402-3. PMID 11890765 DOI: 10.1021/Ja0121686 |
0.76 |
|
| 2002 |
Roh Y, Jang HY, Lynch V, Bauld NL, Krische MJ. Anion radical chain cycloaddition of tethered enones: intramolecular cyclobutanation and Diels-Alder cycloaddition. Organic Letters. 4: 611-3. PMID 11843604 DOI: 10.1021/Ol0172065 |
0.555 |
|
| 2002 |
Archer EA, Cauble DF, Lynch V, Krische MJ. Synthetic duplex oligomers: Optimizing interstrand affinity through the use of a noncovalent constraint Tetrahedron. 58: 721-725. DOI: 10.1016/S0040-4020(01)01090-0 |
0.79 |
|
| 2001 |
Baik TG, Luis AL, Wang LC, Krische MJ. Diastereoselective cobalt-catalyzed aldol and Michael cycloreductions. Journal of the American Chemical Society. 123: 5112-3. PMID 11457348 DOI: 10.1021/Ja0040971 |
0.722 |
|
| 2001 |
Baik TG, Luis AL, Wang LC, Krische MJ. A diastereoselective metal-catalyzed [2+2] cycloaddition of bis-enomes. Journal of the American Chemical Society. 123: 6716-7. PMID 11439068 DOI: 10.1021/Ja010800P |
0.663 |
|
| 2001 |
Archer EA, Sochia AE, Krische MJ. The covalent casting of one-dimensional hydrogen bonding motifs: toward oligomers and polymers of predefined topography. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 2059-65. PMID 11411978 DOI: 10.1002/1521-3765(20010518)7:10<2059::Aid-Chem2059>3.0.Co;2-I |
0.355 |
|
| 2001 |
Archer EA, Gong H, Krische MJ. Hydrogen bonding in noncovalent synthesis: Selectivity and the directed organization of molecular strands Tetrahedron. 57: 1139-1159. DOI: 10.1016/S0040-4020(00)00986-8 |
0.574 |
|
| 2001 |
Archer EA, Gong H, Krische MJ. ChemInform Abstract: Hydrogen Bonding in Noncovalent Synthesis: Selectivity and the Directed Organization of Molecular Strands Cheminform. 32: no-no. DOI: 10.1002/chin.200120285 |
0.526 |
|
| 2000 |
Berl V, Huc I, Khoury RG, Krische MJ, Lehn JM. Interconversion of single and double helices formed from synthetic molecular strands. Nature. 407: 720-3. PMID 11048713 DOI: 10.1038/35037545 |
0.644 |
|
| 2000 |
Berl V, Krische MJ, Huc I, Lehn JM, Schmutz M. Template-induced and molecular recognition directed hierarchical generation of supramolecular assemblies from molecular strands Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 1938-46. PMID 10894393 DOI: 10.1002/1521-3765(20000602)6:11<1938::Aid-Chem1938>3.0.Co;2-Y |
0.59 |
|
| 2000 |
Krische MJ, Lehn J, Kyritsakas N, Fischer J, Wegelius EK, Rissanen K. Self-assembly of 1- and 2-Dimensional Multicompartmental Arrays via the 2-Aminopyrimidine H-Bonding Motif and Selective Guest Inclusion Tetrahedron. 56: 6701-6706. DOI: 10.1016/S0040-4020(00)00489-0 |
0.464 |
|
| 1999 |
Trost B, Krische MJ. Palladium-Catalyzed Enyne Cycloisomerization Reaction in an Asymmetric Approach to the Picrotoxane Sesquiterpenes. 2. Second-Generation Total Syntheses of Corianin, Picrotoxinin, Picrotin, and Methyl Picrotoxate Journal of the American Chemical Society. 121: 6131-6141. DOI: 10.1021/Ja990183T |
0.605 |
|
| 1999 |
Trost BM, Haffner CD, Jebaratnam DJ, Krische MJ, Thomas AP. The Palladium-Catalyzed Enyne Cycloisomerization Reaction in a General Approach to the Asymmetric Syntheses of the Picrotoxane Sesquiterpenes. Part I. First-Generation Total Synthesis of Corianin and Formal Syntheses of Picrotoxinin and Picrotin Journal of the American Chemical Society. 121: 6183-6192. DOI: 10.1021/Ja9901821 |
0.603 |
|
| 1999 |
Krische MJ, Lehn J, Cheung E, Vaughn G, Krische AL. Self-assembly of helical supramolecular channels from chiral aminopyrimidine hydrogen bonding motifs in the solid state Comptes Rendus De L'AcadéMie Des Sciences - Series Iic - Chemistry. 2: 549-556. DOI: 10.1016/S1387-1609(00)88565-5 |
0.48 |
|
| 1999 |
Huc I, Krische MJ, Funeriu DP, Lehn J. Dynamic Combinatorial Chemistry: Substrate H-Bonding Directed Assembly of Receptors Based on Bipyridine-Metal Complexes European Journal of Inorganic Chemistry. 1999: 1415-1420. DOI: 10.1002/(Sici)1099-0682(199909)1999:9<1415::Aid-Ejic1415>3.0.Co;2-Y |
0.643 |
|
| 1998 |
Trost BM, Krische MJ. Transition Metal Catalyzed Cycloisomerizations Synlett. 1998: 1-16. DOI: 10.1055/S-1998-1557 |
0.479 |
|
| 1998 |
Krische MJ, Trost BM. Transformations of the picrotoxanes: The synthesis of corianin and structural analogues from picrotoxinin Tetrahedron. 54: 7109-7120. DOI: 10.1016/S0040-4020(98)00350-0 |
0.487 |
|
| 1998 |
Krische MJ, Trost BM. Total synthesis of methyl picrotoxate via the palladium catalyzed enyne cycloisomerization reaction Tetrahedron. 54: 3693-3704. DOI: 10.1016/S0040-4020(98)00103-3 |
0.581 |
|
| 1998 |
Krische M, Lehn J, Kyritsakas N, Fischer J, Wegelius E, Nissinen M, Rissanen K. Exploring the 2,2′-Diamino-5,5′-bipyrimidine Hydrogen-Bonding Motif: A Modular Approach to Alkoxy-Functionalized Hydrogen-Bonded Networks Helvetica Chimica Acta. 81: 1921-1930. DOI: 10.1002/(Sici)1522-2675(19981111)81:11<1921::Aid-Hlca1921>3.0.Co;2-7 |
0.507 |
|
| 1998 |
Krische M, Lehn J, Kyritsakas N, Fischer J. Molecular-Recognition-Directed Self-Assembly of Pleated Sheets from 2-Aminopyrimidine Hydrogen-Bonding Motifs Helvetica Chimica Acta. 81: 1909-1920. DOI: 10.1002/(Sici)1522-2675(19981111)81:11<1909::Aid-Hlca1909>3.0.Co;2-0 |
0.491 |
|
| 1996 |
Trost BM, Krische MJ, Radinov R, Zanoni G. On Asymmetric Induction in Allylic Alkylation via Enantiotopic Facial Discrimination Journal of the American Chemical Society. 118: 6297-6298. DOI: 10.1021/Ja960649X |
0.552 |
|
| 1996 |
Trost BM, Krische MJ. General Strategy for the Asymmetric Synthesis of the Picrotoxanes Journal of the American Chemical Society. 118: 233-234. DOI: 10.1021/Ja953060R |
0.531 |
|
| 1990 |
Koskinen AMP, Krische MJ. γ-Amino-β-keto Phosphonates in Synthesis: Synthesis of the Sphingosine Skeleton Synlett. 1990: 665-666. DOI: 10.1055/S-1990-21202 |
0.31 |
|
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