| Year |
Citation |
Score |
| 2024 |
Bock MJ, Denmark SE. Rapid, Homogenous, B-Alkyl Suzuki-Miyaura Cross-Coupling of Boronic Esters. The Journal of Organic Chemistry. PMID 38483187 DOI: 10.1021/acs.joc.4c00089 |
0.388 |
|
| 2024 |
Schnitzer T, Schnurr M, Zahrt AF, Sakhaee N, Denmark SE, Wennemers H. Machine Learning to Develop Peptide Catalysts-Successes, Limitations, and Opportunities. Acs Central Science. 10: 367-373. PMID 38435528 DOI: 10.1021/acscentsci.3c01284 |
0.784 |
|
| 2024 |
Delaney CP, Zahrt AF, Kassel VM, Denmark SE. Effects of Ring Size and Steric Encumbrance on Boron-to-Palladium Transmetalation from Arylboronic Esters. The Journal of Organic Chemistry. PMID 38421803 DOI: 10.1021/acs.joc.3c02629 |
0.825 |
|
| 2023 |
Rinehart NI, Saunthwal RK, Wellauer J, Zahrt AF, Schlemper L, Shved AS, Bigler R, Fantasia S, Denmark SE. A machine-learning tool to predict substrate-adaptive conditions for Pd-catalyzed C-N couplings. Science (New York, N.Y.). 381: 965-972. PMID 37651532 DOI: 10.1126/science.adg2114 |
0.79 |
|
| 2022 |
Matviitsuk A, Lee Panger J, Denmark SE. Enantioselective Inter- and Intramolecular Sulfenofunctionalization of Unactivated Cyclic and ()-Alkenes. Acs Catalysis. 12: 7377-7385. PMID 36686398 DOI: 10.1021/acscatal.2c01232 |
0.351 |
|
| 2022 |
Rose BT, Timmerman JC, Bawel SA, Chin S, Zhang H, Denmark SE. High-Level Data Fusion Enables the Chemoinformatically Guided Discovery of Chiral Disulfonimide Catalysts for Atropselective Iodination of 2-Amino-6-arylpyridines. Journal of the American Chemical Society. PMID 36475666 DOI: 10.1021/jacs.2c08820 |
0.339 |
|
| 2022 |
Delaney CP, Marron DP, Shved AS, Zare RN, Waymouth RM, Denmark SE. Potassium Trimethylsilanolate-Promoted, Anhydrous Suzuki-Miyaura Cross-Coupling Reaction Proceeds via the "Boronate Mechanism": Evidence for the Alternative Fork in the Trail. Journal of the American Chemical Society. 144: 4345-4364. PMID 35230833 DOI: 10.1021/jacs.1c08283 |
0.362 |
|
| 2021 |
Hilby KM, Denmark SE. Lewis Base Catalyzed, Sulfenium Ion Initiated Enantioselective, Spiroketalization Cascade. The Journal of Organic Chemistry. 86: 14250-14289. PMID 34672623 DOI: 10.1021/acs.joc.1c02271 |
0.373 |
|
| 2021 |
Menard T, Laverny A, Denmark SE. Synthesis of Enantioenriched 3,4-Disubstituted Chromans through Lewis Base Catalyzed Carbosulfenylation. The Journal of Organic Chemistry. PMID 34672591 DOI: 10.1021/acs.joc.1c02290 |
0.343 |
|
| 2021 |
Rinehart NI, Zahrt AF, Denmark SE. Leveraging Machine Learning for Enantioselective Catalysis: From Dream to Reality. Chimia. 75: 592-597. PMID 34523399 DOI: 10.2533/chimia.2021.592 |
0.782 |
|
| 2021 |
Kassel VM, Hanneman CM, Delaney CP, Denmark SE. Heteroaryl-Heteroaryl, Suzuki-Miyaura, Anhydrous Cross-Coupling Reactions Enabled by Trimethyl Borate. Journal of the American Chemical Society. 143: 13845-13853. PMID 34415757 DOI: 10.1021/jacs.1c06419 |
0.419 |
|
| 2021 |
Mumford EM, Hemric BN, Denmark SE. Catalytic, Enantioselective -Oxyamination of Alkenes. Journal of the American Chemical Society. PMID 34375090 DOI: 10.1021/jacs.1c06750 |
0.832 |
|
| 2021 |
Rinehart NI, Zahrt AF, Henle JJ, Denmark SE. Dreams, False Starts, Dead Ends, and Redemption: A Chronicle of the Evolution of a Chemoinformatic Workflow for the Optimization of Enantioselective Catalysts. Accounts of Chemical Research. PMID 33856771 DOI: 10.1021/acs.accounts.0c00826 |
0.803 |
|
| 2021 |
Shrestha B, Rose BT, Olen CL, Roth A, Kwong AC, Wang Y, Denmark SE. A Unified Strategy for the Asymmetric Synthesis of Highly Substituted 1,2-Amino Alcohols Leading to Highly Substituted Bisoxazoline Ligands. The Journal of Organic Chemistry. PMID 33539091 DOI: 10.1021/acs.joc.0c02899 |
0.78 |
|
| 2020 |
Delaney CP, Kassel VM, Denmark SE. Potassium Trimethylsilanolate Enables Rapid, Homogeneous Suzuki-Miyaura Cross-Coupling of Boronic Esters. Acs Catalysis. 10: 73-80. PMID 33585070 DOI: 10.1021/acscatal.9b04353 |
0.351 |
|
| 2020 |
Athavale SV, Simon A, Houk KN, Denmark SE. Structural Contributions to Autocatalysis and Asymmetric Amplification in the Soai Reaction. Journal of the American Chemical Society. 142: 18387-18406. PMID 33108874 DOI: 10.1021/jacs.0c05994 |
0.323 |
|
| 2020 |
Zahrt AF, Henle JJ, Denmark SE. Cautionary Guidelines for Machine Learning Studies with Combinatorial Datasets. Acs Combinatorial Science. PMID 33000621 DOI: 10.1021/acscombsci.0c00118 |
0.771 |
|
| 2020 |
Henle JJ, Zahrt AF, Rose BT, Darrow WT, Wang Y, Denmark SE. Development of a Computer-Guided Workflow for Catalyst Optimization. Descriptor Validation, Subset Selection, and Training Set Analysis. Journal of the American Chemical Society. PMID 32568531 DOI: 10.1021/jacs.0c04715 |
0.776 |
|
| 2020 |
Matviitsuk AE, Panger JL, Denmark SE. Catalytic, Enantioselective Sulfenofunctionalization of Alkenes- Development and Recent Advances. Angewandte Chemie (International Ed. in English). PMID 32452077 DOI: 10.1002/Anie.202005920 |
0.355 |
|
| 2020 |
Athavale SV, Simon A, Houk KN, Denmark SE. Demystifying the asymmetry-amplifying, autocatalytic behaviour of the Soai reaction through structural, mechanistic and computational studies. Nature Chemistry. PMID 32203445 DOI: 10.1038/S41557-020-0421-8 |
0.308 |
|
| 2019 |
Denmark SE, Ryabchuk P, Chi HM, Matviitsuk A. Preparation of a Diisopropylselenophosphoramide Catalyst and its Use in Enantioselective Sulfenoetherification. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 96: 400-417. PMID 34526731 DOI: 10.15227/orgsyn.096.0400 |
0.757 |
|
| 2019 |
Zahrt AF, Denmark SE. Evaluating continuous chirality measure as a 3D descriptor in chemoinformatics applied to asymmetric catalysis. Tetrahedron Letters. 75: 1841-1851. PMID 31983782 DOI: 10.1016/J.Tet.2019.02.007 |
0.807 |
|
| 2019 |
Zahrt AF, Athavale SV, Denmark SE. Quantitative Structure-Selectivity Relationships in Enantioselective Catalysis: Past, Present, and Future. Chemical Reviews. PMID 31886649 DOI: 10.1021/acs.chemrev.9b00425 |
0.804 |
|
| 2019 |
Panger JL, Denmark SE. Enantioselective Synthesis of γ-Lactams by Lewis Base Catalyzed Sulfenoamidation of Alkenes. Organic Letters. PMID 31858805 DOI: 10.1021/Acs.Orglett.9B04347 |
0.495 |
|
| 2019 |
Bigler R, Mack KA, Shen J, Tosatti P, Han C, Zhang H, Scalone M, Pfaltz A, Denmark SE, Hildbrand S, Gosselin F. Asymmetric Hydrogenation of Unfunctionalized, Tetrasubstituted, Acyclic Olefins. Angewandte Chemie (International Ed. in English). PMID 31794118 DOI: 10.1002/Anie.201912640 |
0.533 |
|
| 2019 |
Gilbert BB, Eey ST, Ryabchuk P, Garry O, Denmark SE. Organoselenium-catalyzed enantioselective -dichlorination of unbiased alkenes. Tetrahedron. 75: 4086-4098. PMID 31768077 DOI: 10.1016/J.Tet.2019.05.054 |
0.48 |
|
| 2019 |
Tao Z, Gilbert BB, Denmark SE. Catalytic, Enantioselective Diamination of Alkenes. Journal of the American Chemical Society. PMID 31742399 DOI: 10.1021/Jacs.9B11261 |
0.539 |
|
| 2019 |
Roth A, Denmark SE. Enantioselective, Lewis Base-Catalyzed, Intermolecular Sulfenoamination of Alkenes. Journal of the American Chemical Society. PMID 31433174 DOI: 10.1021/Jacs.9B07019 |
0.469 |
|
| 2019 |
Denmark SE. Dynamically Chiral Helical Polymers: A New Frontier in Asymmetric Catalysis? Acs Central Science. 5: 1117-1119. PMID 31403066 DOI: 10.1021/Acscentsci.9B00644 |
0.356 |
|
| 2019 |
Matviitsuk A, Denmark SE. Enantio- and Diastereoselective, Lewis Base Catalyzed, Cascade Sulfenoacetalization of Alkenyl Aldehydes. Angewandte Chemie (International Ed. in English). PMID 31295383 DOI: 10.1002/Anie.201906535 |
0.507 |
|
| 2019 |
Zhukhovitskiy AV, Kobylianskii IJ, Thomas AA, Evans AM, Delaney CP, Flanders NC, Denmark SE, Dichtel WR, Toste FD. A Dinuclear Mechanism Implicated in Controlled Carbene Polymerization. Journal of the American Chemical Society. PMID 30964670 DOI: 10.1021/Jacs.9B01532 |
0.347 |
|
| 2019 |
Zahrt AF, Henle JJ, Rose BT, Wang Y, Darrow WT, Denmark SE. Prediction of higher-selectivity catalysts by computer-driven workflow and machine learning. Science (New York, N.Y.). 363. PMID 30655414 DOI: 10.1126/Science.Aau5631 |
0.798 |
|
| 2019 |
Robb KA, Athavale SV, Denmark SE. Unusual Kinetic Profiles for Lewis Base-Catalyzed Sulfenocyclization of ortho-Geranylphenols in Hexafluoroisopropyl Alcohol Synlett. 30: 1656-1661. DOI: 10.1055/S-0039-1690111 |
0.391 |
|
| 2019 |
Delaney CP, Kassel VM, Denmark SE. Potassium Trimethylsilanolate Enables Rapid, Homogeneous Suzuki−Miyaura Cross-Coupling of Boronic Esters Acs Catalysis. 10: 73-80. DOI: 10.1021/Acscatal.9B04353 |
0.398 |
|
| 2019 |
Denmark S. Preparation of a Diisopropylselenophosphoramide Catalyst and its Use in Enantioselective Sulfenoetherification Organic Syntheses. 96: 400-417. DOI: 10.1002/0471264229.Os096.25 |
0.376 |
|
| 2018 |
Tao Z, Robb KA, Panger JL, Denmark SE. Enantioselective, Lewis Base-Catalyzed Carbosulfenylation of Alkenylboronates by 1,2-Boronate Migration. Journal of the American Chemical Society. PMID 30411878 DOI: 10.1021/Jacs.8B10288 |
0.54 |
|
| 2018 |
Ibrahim MYS, Denmark SE. Palladium/Rhodium Cooperative Catalysis for the Production of Aryl Aldehydes and Their Deuterated Analogues Using the Water-Gas Shift Reaction. Angewandte Chemie (International Ed. in English). PMID 30015402 DOI: 10.1002/Anie.201806148 |
0.459 |
|
| 2018 |
Böse D, Denmark SE. Investigating the Enantiodetermining Step of a Chiral Lewis Base Catalyzed Bromocycloetherification of Privileged Alkenes. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 29: 433-439. PMID 29904236 DOI: 10.1055/S-0036-1590951 |
0.477 |
|
| 2018 |
Barraza SJ, Denmark SE. Synthesis, Reactivity, Functionalization, and ADMET Properties of Silicon-Containing Nitrogen Heterocycles. Journal of the American Chemical Society. PMID 29763323 DOI: 10.1021/Jacs.8B03187 |
0.313 |
|
| 2018 |
Thomas AA, Zahrt AF, Delaney CP, Denmark SE. Elucidating the Role of the Boronic Esters in the Suzuki-Miyaura Reaction: Structural, Kinetic, and Computational Investigations. Journal of the American Chemical Society. PMID 29543441 DOI: 10.1021/Jacs.8B00400 |
0.835 |
|
| 2018 |
Tao Z, Robb KA, Zhao K, Denmark SE. Enantioselective, Lewis Base-Catalyzed Sulfenocyclization of Polyenes. Journal of the American Chemical Society. PMID 29509003 DOI: 10.1021/Jacs.8B01660 |
0.502 |
|
| 2017 |
Denmark SE, Chi HM. Synthesis of 2-Alkenyl-Tethered Anilines. Synthesis. 49: 2873-2888. PMID 29937594 DOI: 10.1055/S-0036-1589002 |
0.823 |
|
| 2017 |
Barraza SJ, Denmark SE. Unexpected Rearrangement of 2-Bromoaniline under Biphasic Alkylation Conditions. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 28: 2891-2895. PMID 29904235 DOI: 10.1055/S-0036-1590882 |
0.397 |
|
| 2017 |
Denmark SE, Ambrosi A. Understanding Site Selectivity in the Palladium-Catalyzed Cross-Coupling of Allenylsilanolates. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 28: 2415-2420. PMID 29904234 DOI: 10.1055/S-0036-1588471 |
0.436 |
|
| 2017 |
Hartmann E, Denmark SE. Structural, Mechanistic, Spectroscopic, and Preparative Studies on the Lewis Base Catalyzed, Enantioselective Sulfenofunctionalization of Alkenes. Helvetica Chimica Acta. 100. PMID 29311750 DOI: 10.1002/Hlca.201700158 |
0.67 |
|
| 2017 |
Denmark SE, Matesich ZD, Nguyen ST, Milicevic Sephton S. Catalytic Nucleophilic Allylation Driven by the Water-Gas Shift Reaction. The Journal of Organic Chemistry. PMID 29220183 DOI: 10.1021/Acs.Joc.7B02658 |
0.465 |
|
| 2017 |
Denmark SE, Chi HM. Catalytic, Enantioselective, Intramolecular Sulfenoamination of Alkenes with Anilines. The Journal of Organic Chemistry. PMID 28294614 DOI: 10.1021/Acs.Joc.7B00391 |
0.804 |
|
| 2017 |
Thomas AA, Wang H, Zahrt AF, Denmark SE. Structural, Kinetic, and Computational Characterization of the Elusive Arylpalladium(II)boronate Complexes in the Suzuki-Miyaura Reaction. Journal of the American Chemical Society. PMID 28266847 DOI: 10.1021/Jacs.6B13384 |
0.806 |
|
| 2017 |
Denmark SE, Kornfilt DJ. Catalytic, Enantioselective, Intramolecular Sulfenofunctionalization of Alkenes with Phenols. The Journal of Organic Chemistry. PMID 28257203 DOI: 10.1021/Acs.Joc.7B00295 |
0.513 |
|
| 2016 |
Ambrosi A, Denmark SE. Harnessing the Power of the Water-Gas Shift Reaction for Organic Synthesis. Angewandte Chemie (International Ed. in English). PMID 27595612 DOI: 10.1002/Anie.201601803 |
0.4 |
|
| 2016 |
Denmark SE, Ryabchuk P, Burk MT, Gilbert BB. Toward Catalytic, Enantioselective Chlorolactonization of 1,2-Disubstituted Styrenyl Carboxylic Acids. The Journal of Organic Chemistry. PMID 27555101 DOI: 10.1021/Acs.Joc.6B01455 |
0.417 |
|
| 2016 |
Thomas AA, Denmark SE. Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: The missing link. Science (New York, N.Y.). 352: 329-32. PMID 27081068 DOI: 10.1126/Science.Aad6981 |
0.436 |
|
| 2016 |
Denmark SE, Ibrahim MYS, Ambrosi A. Room Temperature, Reductive Alkylation of Activated Methylene Compounds: Carbon–Carbon Bond Formation Driven by the Rhodium-Catalyzed Water–Gas Shift Reaction Acs Catalysis. 7: 613-630. DOI: 10.1021/Acscatal.6B03183 |
0.468 |
|
| 2016 |
Denmark SE, Carson N. ChemInform Abstract: Reinvestigation of a Catalytic, Enantioselective Alkene Dibromination and Chlorohydroxylation. Cheminform. 47. DOI: 10.1002/chin.201616045 |
0.84 |
|
| 2016 |
Cresswell AJ, Eey ST, Denmark SE. ChemInform Abstract: Catalytic, Stereoselective Dihalogenation of Alkenes: Challenges and Opportunities Cheminform. 47: no-no. DOI: 10.1002/chin.201608253 |
0.771 |
|
| 2015 |
Cresswell AJ, Eey ST, Denmark SE. Catalytic, Stereoselective Dihalogenation of Alkenes: Challenges and Opportunities. Angewandte Chemie (International Ed. in English). PMID 26630449 DOI: 10.1002/Anie.201507152 |
0.765 |
|
| 2015 |
Denmark SE, Carson N. Reinvestigation of a Catalytic, Enantioselective Alkene Dibromination and Chlorohydroxylation. Organic Letters. PMID 26566099 DOI: 10.1021/Acs.Orglett.5B02650 |
0.825 |
|
| 2015 |
Denmark SE, Ambrosi A. Why You Really Should Consider Using Palladium-Catalyzed Cross-Coupling of Silanols and Silanolates. Organic Process Research & Development. 19: 982-994. PMID 26478695 DOI: 10.1021/Acs.Oprd.5B00201 |
0.471 |
|
| 2015 |
Denmark SE, Cullen LR. Development of a Phase-Transfer-Catalyzed, [2,3]-Wittig Rearrangement. The Journal of Organic Chemistry. PMID 26431154 DOI: 10.1021/Acs.Joc.5B01759 |
0.356 |
|
| 2015 |
Tymonko SA, Smith RC, Ambrosi A, Ober MH, Wang H, Denmark SE. Mechanistic significance of the si-o-pd bond in the palladium-catalyzed cross-coupling reactions of arylsilanolates. Journal of the American Chemical Society. 137: 6200-18. PMID 25945516 DOI: 10.1021/Jacs.5B02518 |
0.797 |
|
| 2015 |
Tymonko SA, Smith RC, Ambrosi A, Denmark SE. Mechanistic significance of the si-o-pd bond in the palladium-catalyzed cross-coupling reactions of alkenylsilanolates. Journal of the American Chemical Society. 137: 6192-9. PMID 25945390 DOI: 10.1021/Jacs.5B02515 |
0.811 |
|
| 2015 |
Denmark SE, Chang WT, Houk KN, Liu P. Development of Chiral Bis-hydrazone Ligands for the Enantioselective Cross-Coupling Reactions of Aryldimethylsilanolates. The Journal of Organic Chemistry. 80: 313-66. PMID 25494058 DOI: 10.1021/Jo502388R |
0.5 |
|
| 2015 |
List B, Höfler D, Denmark SE, Hartmann E, Kornfilt DJP, Wang H. Catalytic, Enantioselective Sulfenofunctionalization of Alkenes Synfacts. 11: 204-204. DOI: 10.1055/S-0034-1379818 |
0.474 |
|
| 2015 |
Denmark SE, Ambrosi A. ChemInform Abstract: Why You Really Should Consider Using Palladium-Catalyzed Cross-Coupling of Silanols and Silanolates Cheminform. 46: no-no. DOI: 10.1002/chin.201542251 |
0.313 |
|
| 2015 |
Denmark SE, Hartmann E, Kornfilt DJP, Wang H. ChemInform Abstract: Mechanistic, Crystallographic, and Computational Studies on the Catalytic, Enantioselective Sulfenofunctionalization of Alkenes. Cheminform. 46: no-no. DOI: 10.1002/chin.201520088 |
0.606 |
|
| 2015 |
Cresswell AJ, Eey ST, Denmark SE. ChemInform Abstract: Catalytic, Stereospecific syn-Dichlorination of Alkenes. Cheminform. 46: no-no. DOI: 10.1002/chin.201519058 |
0.776 |
|
| 2015 |
Denmark SE, Chang WT, Houk KN, Liu P. ChemInform Abstract: Development of Chiral Bis-hydrazone Ligands for the Enantioselective Cross-Coupling Reactions of Aryldimethylsilanolates. Cheminform. 46: no-no. DOI: 10.1002/chin.201514026 |
0.39 |
|
| 2015 |
Denmark SE, Rossi S, Webster MP, Wang H. ChemInform Abstract: Catalytic, Enantioselective Sulfenylation of Ketone-Derived Enoxysilanes. Cheminform. 46: no-no. DOI: 10.1002/chin.201514023 |
0.403 |
|
| 2015 |
Denmark SE, Wilson TW, Burk MT. ChemInform Abstract: Enantioselective Construction of Quaternary Stereogenic Carbon Atoms by the Lewis Base Catalyzed Additions of Silyl Ketene Imines to Aldehydes. Cheminform. 46: no-no. DOI: 10.1002/chin.201506105 |
0.586 |
|
| 2015 |
Denmark SE, Chi HM. ChemInform Abstract: Lewis Base Catalyzed, Enantioselective, Intramolecular Sulfenoamination of Olefins. Cheminform. 46: no-no. DOI: 10.1002/chin.201505159 |
0.82 |
|
| 2015 |
Cresswell AJ, Eey ST, Denmark SE. Katalytische stereoselektive Dihalogenierung von Alkenen: Herausforderungen und Chancen Angewandte Chemie. 127: 15866-15909. DOI: 10.1002/Ange.201507152 |
0.696 |
|
| 2014 |
Cresswell AJ, Eey ST, Denmark SE. Catalytic, stereospecific syn-dichlorination of alkenes. Nature Chemistry. 7: 146-52. PMID 25615668 DOI: 10.1038/Nchem.2141 |
0.796 |
|
| 2014 |
Denmark SE, Hartmann E, Kornfilt DJ, Wang H. Mechanistic, crystallographic, and computational studies on the catalytic, enantioselective sulfenofunctionalization of alkenes. Nature Chemistry. 6: 1056-64. PMID 25411883 DOI: 10.1038/Nchem.2109 |
0.616 |
|
| 2014 |
Denmark SE, Rossi S, Webster MP, Wang H. Catalytic, enantioselective sulfenylation of ketone-derived enoxysilanes. Journal of the American Chemical Society. 136: 13016-28. PMID 25192220 DOI: 10.1021/Ja506133Z |
0.509 |
|
| 2014 |
Denmark SE, Wilson TW, Burk MT. Enantioselective construction of quaternary stereogenic carbon atoms by the Lewis base catalyzed additions of silyl ketene imines to aldehydes. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 9268-79. PMID 25043283 DOI: 10.1002/Chem.201403342 |
0.707 |
|
| 2014 |
Denmark SE, Matesich ZD. Catalytic, nucleophilic allylation of aldehydes with 2-substituted allylic acetates: carbon-carbon bond formation driven by the water-gas shift reaction. The Journal of Organic Chemistry. 79: 5970-86. PMID 24927196 DOI: 10.1021/Jo501004J |
0.481 |
|
| 2014 |
Denmark SE, Chi HM. Lewis base catalyzed, enantioselective, intramolecular sulfenoamination of olefins. Journal of the American Chemical Society. 136: 8915-8. PMID 24926794 DOI: 10.1021/Ja5046296 |
0.828 |
|
| 2014 |
Denmark SE, Chi HM. Catalytic, enantioselective, intramolecular carbosulfenylation of olefins. Mechanistic aspects: a remarkable case of negative catalysis. Journal of the American Chemical Society. 136: 3655-63. PMID 24548006 DOI: 10.1021/Ja413270H |
0.813 |
|
| 2014 |
Denmark SE, Burk MT. Development and mechanism of an enantioselective bromocycloetherification reaction via Lewis base/chiral Brønsted acid cooperative catalysis. Chirality. 26: 344-55. PMID 24395341 DOI: 10.1002/Chir.22259 |
0.468 |
|
| 2014 |
Denmark SE, Cullen LR. Catalytic conjugate addition of acyl anion equivalents promoted by fluorodesilylation. Organic Letters. 16: 70-3. PMID 24328533 DOI: 10.1021/Ol403041K |
0.514 |
|
| 2014 |
Denmark SE, Jaunet A. Catalytic, enantioselective, intramolecular carbosulfenylation of olefins. Preparative and stereochemical aspects. The Journal of Organic Chemistry. 79: 140-71. PMID 24328051 DOI: 10.1021/Jo4023765 |
0.486 |
|
| 2014 |
Denmark SE, Cresswell AJ. ChemInform Abstract: Iron-Catalyzed Cross-Coupling of Unactivated Secondary Alkyl Thio Ethers and Sulfones with Aryl Grignard Reagents. Cheminform. 45: no-no. DOI: 10.1002/chin.201422104 |
0.76 |
|
| 2014 |
Denmark SE, Jaunet A. ChemInform Abstract: Catalytic, Enantioselective, Intramolecular Carbosulfenylation of Olefins. Preparative and Stereochemical Aspects. Cheminform. 45: no-no. DOI: 10.1002/chin.201422095 |
0.415 |
|
| 2014 |
Denmark SE, Cullen LR. ChemInform Abstract: Catalytic Conjugate Addition of Acyl Anion Equivalents Promoted by Fluorodesilylation. Cheminform. 45: no-no. DOI: 10.1002/chin.201422029 |
0.321 |
|
| 2014 |
Denmark SE, Marble LK. ChemInform Abstract: Asymmetric Construction of Quaternary Stereogenic Centers via Auxiliary-Based SN2′ Reactions: A Case of 1,7-Relative Stereogenesis. Cheminform. 45: no-no. DOI: 10.1002/chin.201421042 |
0.312 |
|
| 2014 |
West R, Samedov K, Percival PW, Jutzi P, Denmark SE, Wilson TW, Burk MT, Pinkert D, Limberg C, Büchner C, Lichtenstein L, Yu X, Boscoboinik JA, Yang B, Kaden WE, et al. Cover Picture: Silicon Meets Cyclotron: Muon Spin Resonance of Organosilicon Radicals / The Pentamethylcyclopentadienylsilicon(II) Cation: Synthesis, Characterization, and Reactivity / Enantioselective Construction of Quaternary Stereogenic Carbon Atoms b Chemistry - a European Journal. 20: 9141-9141. DOI: 10.1002/Chem.201490122 |
0.575 |
|
| 2014 |
Baiazitov RY, Denmark SE. Tandem [4+2]/[3+2] Cycloadditions Methods and Applications of Cycloaddition Reactions in Organic Syntheses. 471-550. DOI: 10.1002/9781118778173.ch16 |
0.751 |
|
| 2013 |
Denmark SE, Ueki Y. Lewis Base Activation of Lewis Acids - Group 13. In Situ Generation and Reaction of Borenium Ions. Organometallics. 32. PMID 24347789 DOI: 10.1021/Om400582K |
0.325 |
|
| 2013 |
Denmark SE, Cresswell AJ. Iron-catalyzed cross-coupling of unactivated secondary alkyl thio ethers and sulfones with aryl Grignard reagents. The Journal of Organic Chemistry. 78: 12593-628. PMID 24256193 DOI: 10.1021/Jo402246H |
0.807 |
|
| 2013 |
Beutner GL, Denmark SE. Lewis base catalysis of the Mukaiyama directed aldol reaction: 40 years of inspiration and advances. Angewandte Chemie (International Ed. in English). 52: 9086-96. PMID 23843275 DOI: 10.1002/Anie.201302084 |
0.741 |
|
| 2013 |
Denmark SE, Jaunet A. Catalytic, enantioselective, intramolecular carbosulfenylation of olefins. Journal of the American Chemical Society. 135: 6419-22. PMID 23597174 DOI: 10.1021/Ja401867B |
0.512 |
|
| 2013 |
Wolf LM, Denmark SE. A theoretical investigation on the mechanism and stereochemical course of the addition of (E)-2-butenyltrimethylsilane to acetaldehyde by electrophilic and nucleophilic activation. Journal of the American Chemical Society. 135: 4743-56. PMID 23484480 DOI: 10.1021/Ja311889V |
0.539 |
|
| 2013 |
Denmark SE, Marlin JE, Rajendra G. Carbanion-accelerated Claisen rearrangements: asymmetric induction with chiral phosphorus-stabilized anions. The Journal of Organic Chemistry. 78: 66-82. PMID 23101563 DOI: 10.1021/Jo301919E |
0.427 |
|
| 2013 |
Beutner GL, Denmark SE. The interplay of invention, observation, and discovery in the development of lewis base activation of lewis acids for catalytic enantioselective synthesis Topics in Organometallic Chemistry. 44: 55-89. DOI: 10.1007/3418-2012-43 |
0.699 |
|
| 2013 |
Beutner GL, Denmark SE. ChemInform Abstract: Lewis Base Catalysis of the Mukaiyama Directed Aldol Reaction: 40 Years of Inspiration and Advances Cheminform. 44: no-no. DOI: 10.1002/chin.201347233 |
0.693 |
|
| 2013 |
Denmark SE, Jaunet A. ChemInform Abstract: Catalytic, Enantioselective, Intramolecular Carbosulfenylation of Olefins. Cheminform. 44: no-no. DOI: 10.1002/chin.201339087 |
0.419 |
|
| 2013 |
Denmark SE, Kuester WE, Burk MT. ChemInform Abstract: Catalytic, Asymmetric Halofunctionalization of Alkenes - A Critical Perspective Cheminform. 44: no-no. DOI: 10.1002/chin.201310227 |
0.324 |
|
| 2013 |
Denmark SE, Wilson TW. ChemInform Abstract: Silyl Ketene Imines: Highly Versatile Nucleophiles for Catalytic, Asymmetric Synthesis Cheminform. 44: no-no. DOI: 10.1002/chin.201310219 |
0.683 |
|
| 2013 |
Beutner GL, Denmark SE. Lewis‐Base‐Katalyse der gerichteten Mukaiyama‐Aldolreaktion: 40 Jahre Inspiration und Fortschritt Angewandte Chemie. 125: 9256-9266. DOI: 10.1002/Ange.201302084 |
0.638 |
|
| 2012 |
Denmark SE, Kuester WE, Burk MT. Catalytic, asymmetric halofunctionalization of alkenes--a critical perspective. Angewandte Chemie (International Ed. in English). 51: 10938-53. PMID 23011853 DOI: 10.1002/Anie.201204347 |
0.433 |
|
| 2012 |
Denmark SE, Wilson TW. Silyl ketene imines: highly versatile nucleophiles for catalytic, asymmetric synthesis. Angewandte Chemie (International Ed. in English). 51: 9980-92. PMID 22968901 DOI: 10.1002/Anie.201202139 |
0.706 |
|
| 2012 |
Denmark SE, Wilson TW. Lewis base catalyzed enantioselective additions of an N-silyl vinylketene imine. Angewandte Chemie (International Ed. in English). 51: 3236-9. PMID 22351382 DOI: 10.1002/Anie.201108795 |
0.693 |
|
| 2012 |
Denmark SE, Burk MT. Enantioselective bromocycloetherification by Lewis base/chiral Brønsted acid cooperative catalysis. Organic Letters. 14: 256-9. PMID 22145621 DOI: 10.1021/Ol203033K |
0.474 |
|
| 2012 |
Denmark SE, Weber EJ, Almstead NG, Wolf LM. On the stereochemical course of the addition of allylsilanes to aldehydes Tetrahedron. 68: 7701-7718. DOI: 10.1016/J.Tet.2012.05.084 |
0.562 |
|
| 2012 |
Kobayashi T, Regens CS, Denmark SE. Chapter 4 - Total Synthesis of Papulacandin D Strategies and Tactics in Organic Synthesis. 8. DOI: 10.1016/B978-0-12-386540-3.00005-8 |
0.41 |
|
| 2012 |
Denmark SE, Wilson TW. ChemInform Abstract: Lewis Base Catalyzed Enantioselective Additions of an N-Silyl Vinylketene Imine. Cheminform. 43: no-no. DOI: 10.1002/chin.201233075 |
0.61 |
|
| 2012 |
Denmark SE, Burk MT. ChemInform Abstract: Enantioselective Bromocycloetherification by Lewis Base/Chiral Broensted Acid Cooperative Catalysis. Cheminform. 43: no-no. DOI: 10.1002/chin.201222094 |
0.301 |
|
| 2012 |
Denmark SE, Kornfilt DJP, Vogler T. ChemInform Abstract: Catalytic Asymmetric Thiofunctionalization of Unactivated Alkenes. Cheminform. 43: no-no. DOI: 10.1002/chin.201212031 |
0.378 |
|
| 2012 |
Chang WT, Smith RC, Regens CS, Bailey AD, Werner NS, Denmark SE. ChemInform Abstract: Cross-Coupling with Organosilicon Compounds Cheminform. 43: no-no. DOI: 10.1002/chin.201206257 |
0.789 |
|
| 2012 |
Denmark SE, Wilson TW. Silylketenimine - vielseitige Nucleophile für die katalytische asymmetrische Synthese Angewandte Chemie. 124: 10120-10132. DOI: 10.1002/Ange.201202139 |
0.576 |
|
| 2012 |
Denmark SE, Liu JH. Discussion Addendum for: Palladium Catalyzed Cross‐Coupling of (Z)‐1‐Heptenyldimethylsilanol with 4‐Iodoanisole: (Z)‐(1‐Heptenyl)‐4‐Methoxybenzene Organic Syntheses. 102-108. DOI: 10.1002/0471264229.Os088.10 |
0.605 |
|
| 2011 |
Denmark SE, Kornfilt DJ, Vogler T. Catalytic asymmetric thiofunctionalization of unactivated alkenes. Journal of the American Chemical Society. 133: 15308-11. PMID 21859086 DOI: 10.1021/Ja2064395 |
0.447 |
|
| 2011 |
Denmark SE, Werner NS. γ-Selective cross-coupling of allylic silanolate salts with aromatic bromides using trialkylphosphonium tetrafluoroborate salts prepared directly from phosphine•borane adducts. Organic Letters. 13: 4596-9. PMID 21830766 DOI: 10.1021/Ol2017998 |
0.76 |
|
| 2011 |
Denmark SE, Smith RC, Chang WT. Probing the Electronic Demands of Transmetalation in the Palladium-Catalyzed Cross-Coupling of Arylsilanolates. Tetrahedron. 67: 4391-4396. PMID 21731114 DOI: 10.1016/J.Tet.2011.03.066 |
0.603 |
|
| 2011 |
Denmark SE, Regens CS. Cross-Coupling Reactions of Alkenylsilanols with Fluoroalkylsulfonates: Development and Optimization of a Mild and Stereospecific Coupling Process. Tetrahedron Letters. 52: 2165-2168. PMID 21516201 DOI: 10.1016/J.Tetlet.2010.11.133 |
0.817 |
|
| 2011 |
Denmark SE, Gould ND, Wolf LM. A systematic investigation of quaternary ammonium ions as asymmetric phase-transfer catalysts. Application of quantitative structure activity/selectivity relationships. The Journal of Organic Chemistry. 76: 4337-57. PMID 21446723 DOI: 10.1021/Jo2005457 |
0.631 |
|
| 2011 |
Denmark SE, Gould ND, Wolf LM. A systematic investigation of quaternary ammonium ions as asymmetric phase-transfer catalysts. Synthesis of catalyst libraries and evaluation of catalyst activity. The Journal of Organic Chemistry. 76: 4260-336. PMID 21446721 DOI: 10.1021/Jo2005445 |
0.619 |
|
| 2011 |
Denmark SE, Liu JH, Muhuhi JM. Stereocontrolled total syntheses of isodomoic acids G and H via a unified strategy. The Journal of Organic Chemistry. 76: 201-15. PMID 21121685 DOI: 10.1021/Jo101790Z |
0.627 |
|
| 2011 |
Denmark S, Wilson T. Lewis Base Catalyzed Asymmetric Aldol Addition of Oxyketene Imines to Aldehydes Synfacts. 2011: 0177-0177. DOI: 10.1055/s-0030-1259261 |
0.689 |
|
| 2011 |
Denmark SE, Werner NS. ChemInform Abstract: γ-Selective Cross-Coupling of Allylic Silanolate Salts with Aromatic Bromides Using Trialkylphosphonium Tetrafluoroborate Salts Prepared Directly from Phosphine·Borane Adducts. Cheminform. 43: no-no. DOI: 10.1002/chin.201201047 |
0.745 |
|
| 2011 |
Denmark SE, Regens CS. ChemInform Abstract: Cross-Coupling Reactions of Alkenylsilanols with Fluoroalkylsulfonates: Development and Optimization of a Mild and Stereospecific Coupling Process. Cheminform. 42: no-no. DOI: 10.1002/chin.201131062 |
0.8 |
|
| 2011 |
Denmark SE, Liu JH. ChemInform Abstract: Sequential Processes in Palladium-Catalyzed Silicon-Based Cross-Coupling Cheminform. 42: no-no. DOI: 10.1002/chin.201124230 |
0.549 |
|
| 2011 |
Chang WTT, Smith RC, Regens CS, Bailey AD, Werner NS, Denmark SE. Cross-coupling with organosilicon compounds Organic Reactions. 75: 213-745. DOI: 10.1002/0471264180.Or075.03 |
0.831 |
|
| 2010 |
Denmark SE, Liu JH. Sequential Processes in Palladium-Catalyzed Silicon-Based Cross-Coupling. Israel Journal of Chemistry. 50: 577-587. PMID 23293392 DOI: 10.1002/Ijch.201000036 |
0.604 |
|
| 2010 |
Denmark SE, Wilson TW. N-silyl oxyketene imines are underused yet highly versatile reagents for catalytic asymmetric synthesis. Nature Chemistry. 2: 937-43. PMID 20966949 DOI: 10.1038/Nchem.857 |
0.717 |
|
| 2010 |
Denmark SE, Kalyani D, Collins WR. Preparative and mechanistic studies toward the rational development of catalytic, enantioselective selenoetherification reactions. Journal of the American Chemical Society. 132: 15752-65. PMID 20961070 DOI: 10.1021/Ja106837B |
0.741 |
|
| 2010 |
Denmark SE, Kobayashi T, Regens CS. Total Synthesis of (+)-Papulacandin D. Tetrahedron. 66: 4745-4759. PMID 20711516 DOI: 10.1016/J.Tet.2010.03.093 |
0.835 |
|
| 2010 |
Denmark SE, Burk MT. Lewis base catalysis of bromo- and iodolactonization, and cycloetherification. Proceedings of the National Academy of Sciences of the United States of America. 107: 20655-60. PMID 20705900 DOI: 10.1073/Pnas.1005296107 |
0.48 |
|
| 2010 |
Denmark SE, Williams BJ, Eklov BM, Pham SM, Beutner GL. Design, validation, and implementation of a rapid-injection NMR system. The Journal of Organic Chemistry. 75: 5558-72. PMID 20672809 DOI: 10.1021/Jo100837A |
0.735 |
|
| 2010 |
Denmark SE, Muhuhi JM. Development of a general, sequential, ring-closing metathesis/intramolecular cross-coupling reaction for the synthesis of polyunsaturated macrolactones. Journal of the American Chemical Society. 132: 11768-78. PMID 20666473 DOI: 10.1021/Ja1047363 |
0.492 |
|
| 2010 |
Denmark SE, Liu JH. Silicon-based cross-coupling reactions in the total synthesis of natural products. Angewandte Chemie (International Ed. in English). 49: 2978-86. PMID 20333628 DOI: 10.1002/Anie.200905657 |
0.651 |
|
| 2010 |
Denmark SE, Werner NS. On the stereochemical course of palladium-catalyzed cross-coupling of allylic silanolate salts with aromatic bromides. Journal of the American Chemical Society. 132: 3612-20. PMID 20163185 DOI: 10.1021/Ja910804U |
0.785 |
|
| 2010 |
Denmark SE, Burk MT, Hoover AJ. On the absolute configurational stability of bromonium and chloronium ions. Journal of the American Chemical Society. 132: 1232-3. PMID 20058922 DOI: 10.1021/Ja909965H |
0.352 |
|
| 2010 |
Denmark SE, Smith RC. Mechanistic duality in palladium-catalyzed cross-coupling reactions of aryldimethylsilanolates. intermediacy of an 8-Si-4 arylpalladium(II) silanolate. Journal of the American Chemical Society. 132: 1243-5. PMID 20058920 DOI: 10.1021/Ja907049Y |
0.593 |
|
| 2010 |
Denmark SE, Weintraub RC. Deconstructing quinine. Part 1. Toward an understanding of the remarkable performance of cinchona alkaloids in asymmetric phase transfer catalysis Heterocycles. 82: 1527-1540. DOI: 10.3987/Com-10-S(E)108 |
0.404 |
|
| 2010 |
Denmark S, Kalyani D, Collins W. Lewis Base Catalyzed Asymmetric Selenoetherification Synfacts. 2011: 0047-0047. DOI: 10.1055/S-0030-1259178 |
0.736 |
|
| 2010 |
Denmark SE, Wilson TW. Construction of quaternary stereogenic carbon centers by the Lewis base catalyzed conjugate addition of silyl ketene imines to α,β- unsaturated aldehydes and ketones Synlett. 1723-1728. DOI: 10.1055/S-0029-1219963 |
0.656 |
|
| 2010 |
Denmark SE, Edwards JP, Weber T, Piotrowski DW. Organocerium additions to proline-derived hydrazones: Synthesis of enantiomerically enriched amines Tetrahedron Asymmetry. 21: 1278-1302. DOI: 10.1016/J.Tetasy.2010.04.042 |
0.461 |
|
| 2010 |
Denmark SE, Wilson TW. ChemInform Abstract: Construction of Quaternary Stereogenic Carbon Centers by the Lewis Base Catalyzed Conjugate Addition of Silyl Ketene Imines to α,β-Unsaturated Aldehydes and Ketones. Cheminform. 41: no-no. DOI: 10.1002/chin.201046068 |
0.575 |
|
| 2010 |
Denmark SE, Werner NS. ChemInform Abstract: On the Stereochemical Course of Palladium-Catalyzed Cross-Coupling of Allylic Silanolate Salts with Aromatic Bromides. Cheminform. 41: no-no. DOI: 10.1002/chin.201030058 |
0.756 |
|
| 2010 |
Denmark SE, Liu JH. ChemInform Abstract: Silicon-Based Cross-Coupling Reactions in the Total Synthesis of Natural Products Cheminform. 41: no-no. DOI: 10.1002/chin.201029242 |
0.591 |
|
| 2010 |
Denmark SE, Liu JH, Muhuhi JM. ChemInform Abstract: Total Syntheses of Isodomoic Acids G (Ia) and H (Ib). Cheminform. 41. DOI: 10.1002/chin.201007195 |
0.432 |
|
| 2010 |
Denmark SE, Sweis RF. ChemInform Abstract: Design and Implementation of New, Silicon-Based, Cross-Coupling Reactions: Importance of Silicon-Oxygen Bonds. Cheminform. 33: no-no. DOI: 10.1002/chin.200251255 |
0.731 |
|
| 2010 |
Denmark SE, Fu J. ChemInform Abstract: Asymmetric Construction of Quaternary Centers by Enantioselective Allylation: Application to the Synthesis of the Serotonin Antagonist LY426965. Cheminform. 33: no-no. DOI: 10.1002/chin.200242031 |
0.535 |
|
| 2010 |
Denmark SE, Pan W. ChemInform Abstract: Efficient and Stereoselective Cross-Coupling with Highly Substituted Alkenylsilanols. Cheminform. 33: no-no. DOI: 10.1002/chin.200241088 |
0.323 |
|
| 2010 |
Denmark SE, Matsuhashi H. ChemInform Abstract: Chiral Fluoro Ketones for Catalytic Asymmetric Epoxidation of Alkenes with Oxone. Cheminform. 33: no-no. DOI: 10.1002/chin.200240113 |
0.411 |
|
| 2010 |
Denmark SE, Yang S. ChemInform Abstract: Intramolecular Silicon-Assisted Cross-Coupling Reactions: General Synthesis of Medium-Sized Rings Containing a 1,3-cis-cis Diene Unit. Cheminform. 33: no-no. DOI: 10.1002/chin.200231034 |
0.31 |
|
| 2010 |
Denmark SE, Ghosh SK. ChemInform Abstract: The First Catalytic, Diastereoselective and Enantioselective Crossed-Aldol Reactions of Aldehydes. Cheminform. 33: no-no. DOI: 10.1002/chin.200220025 |
0.423 |
|
| 2010 |
Denmark SE, Fu J. ChemInform Abstract: Catalytic, Enantioselective Addition of Substituted Allylic Trichlorosilanes Using a Rationally-Designed 2,2′-Bispyrrolidine-Based Bisphosphoramide Cheminform. 33: no-no. DOI: 10.1002/chin.200204079 |
0.55 |
|
| 2010 |
Denmark SE, Pham SM. ChemInform Abstract: Highly Diastereoselective Aldol Additions of a Chiral Ethyl Ketone Enolate under Lewis Base Catalysis. Cheminform. 32: no-no. DOI: 10.1002/chin.200144034 |
0.661 |
|
| 2010 |
Denmark SE, Fujimori S. ChemInform Abstract: Diastereoselective Aldol Addition Reactions of a Chiral Methyl Ketone Trichlorosilyl Enolate under Lewis Base Catalysis. Cheminform. 32: no-no. DOI: 10.1002/chin.200142110 |
0.645 |
|
| 2010 |
Denmark SE, Sweis RF. ChemInform Abstract: Fluoride-Free Cross-Coupling of Organosilanols. Cheminform. 32: no-no. DOI: 10.1002/chin.200141083 |
0.723 |
|
| 2010 |
Denmark SE, Wynn T. ChemInform Abstract: Lewis Base Activation of Lewis Acids: Catalytic Enantioselective Allylation and Propargylation of Aldehydes. Cheminform. 32: no-no. DOI: 10.1002/chin.200141031 |
0.331 |
|
| 2010 |
Denmark SE, Yang S. ChemInform Abstract: Sequential Ring-Closing Metathesis and Silicon-Assisted Cross-Coupling Reactions: Stereocontrolled Synthesis of Highly Substituted Unsaturated Alcohols. Cheminform. 32: no-no. DOI: 10.1002/chin.200137095 |
0.377 |
|
| 2010 |
Denmark SE, Wang Z. ChemInform Abstract: Highly Stereoselective Hydrocarbation of Terminal Alkynes via Pt-Catalyzed Hydrosilylation/Pd-Catalyzed Cross-Coupling Reactions. Cheminform. 32: no-no. DOI: 10.1002/chin.200128047 |
0.326 |
|
| 2010 |
Denmark SE, Stavenger RA. ChemInform Abstract: Asymmetric Catalysis of Aldol Reactions with Chiral Lewis Bases Cheminform. 31: no-no. DOI: 10.1002/chin.200036273 |
0.76 |
|
| 2010 |
Denmark SE, Herbert B. ChemInform Abstract: Synthesis of (-)-7-Epiaustraline and (-)-1-Epicastanospermine. Cheminform. 31: no-no. DOI: 10.1002/chin.200035194 |
0.303 |
|
| 2010 |
Denmark SE, Wehrli D. ChemInform Abstract: Highly Stereospecific, Palladium-Catalyzed Cross-Coupling of Alkenylsilanols. Cheminform. 31: no-no. DOI: 10.1002/chin.200021067 |
0.333 |
|
| 2010 |
Denmark SE, Wu Z. ChemInform Abstract: Synthesis of Unsymmetrical Biaryls from Arylsilacyclobutanes. Cheminform. 31: no-no. DOI: 10.1002/chin.200005102 |
0.742 |
|
| 2010 |
Denmark SE, Hurd AR. ChemInform Abstract: Synthesis of (+)-Casuarine. Cheminform. 31: no-no. DOI: 10.1002/chin.200004228 |
0.776 |
|
| 2010 |
Denmark SE, Choi JY. ChemInform Abstract: Highly Stereospecific, Cross-Coupling Reactions of Alkenylsilacyclobutanes. Cheminform. 30: no-no. DOI: 10.1002/chin.199941050 |
0.35 |
|
| 2010 |
Denmark SE, Wu Z. ChemInform Abstract: The Development of Chiral, Nonracemic Dioxiranes for the Catalytic, Enantioselective Epoxidation of Alkenes Cheminform. 30: no-no. DOI: 10.1002/chin.199939261 |
0.761 |
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| 2010 |
Denmark SE, Stavenger RA, Wong K, Su X. ChemInform Abstract: Chiral Phosphoramide-Catalyzed Aldol Additions of Ketone Enolates. Preparative Aspects. Cheminform. 30: no-no. DOI: 10.1002/chin.199938047 |
0.758 |
|
| 2010 |
Denmark SE, Martinborough EA. ChemInform Abstract: Enantioselective Total Syntheses of (+)-Castanospermine, (+)-6-Epicastanospermine, (+)-Australine, and (+)-3-Epiaustraline Cheminform. 30: no-no. DOI: 10.1002/chin.199929211 |
0.336 |
|
| 2010 |
Denmark SE, Stavenger RA, Winter SBD, Wong K, Barsanti PA. ChemInform Abstract: The Chemistry of Chlorosilyl Enolates. Part 9. Preparation of Chlorosilyl Enolates. Cheminform. 30: no-no. DOI: 10.1002/chin.199924057 |
0.81 |
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| 2010 |
Denmark SE, Stavenger RA. ChemInform Abstract: The Chemistry of Trichlorosilyl Enolates. Part 8. Highly 1,4-Syn Diastereoselective, Phosphoramide-Catalyzed Aldol Additions of Chiral Methyl Ketone Enolates. Cheminform. 30: no-no. DOI: 10.1002/chin.199924035 |
0.743 |
|
| 2010 |
Denmark SE, Su X, Nishigaichi Y. ChemInform Abstract: The Chemistry of Trichlorosilyl Enolates. Part 6. Mechanistic Duality in the Lewis Base-Catalyzed Aldol Addition Reaction. Cheminform. 30: no-no. DOI: 10.1002/chin.199921035 |
0.402 |
|
| 2010 |
DENMARK SE, STAVENGER RA, WONG K. ChemInform Abstract: The Chemistry of Trichlorosilyl Enolates. Part 5. Asymmetric Aldol Additions Catalyzed by Chiral Phosphoramides: Electronic Effects of the Aldehyde Component. Cheminform. 29: no-no. DOI: 10.1002/chin.199849053 |
0.722 |
|
| 2010 |
DENMARK SE, HURD AR. ChemInform Abstract: Tandem [4 + 2]/[3 + 2] Cycloadditions with Nitroethylene. Cheminform. 29: no-no. DOI: 10.1002/chin.199835061 |
0.762 |
|
| 2010 |
DENMARK SE, BARSANTI PA, WONG K, STAVENGER RA. ChemInform Abstract: Enantioselective Ring Opening of Epoxides with Silicon Tetrachloride in the Presence of a Chiral Lewis Base. Cheminform. 29: no-no. DOI: 10.1002/chin.199834077 |
0.818 |
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| 2010 |
DENMARK SE, WU Z. ChemInform Abstract: Catalytic Epoxidation of Alkenes with Oxone. Part 3. 6-Oxo-1,1,4,4-tetramethyl-1,4-diazepinium Salts. A New Class of Catalysts for Efficient Epoxidation of Olefins with Oxone. Cheminform. 29: no-no. DOI: 10.1002/chin.199833151 |
0.736 |
|
| 2010 |
DENMARK SE, WU Z, CRUDDEN CM, MATSUHASHI H. ChemInform Abstract: Catalytic Epoxidation of Alkenes with Oxone. Part 2. Fluoro Ketones. Cheminform. 29: no-no. DOI: 10.1002/chin.199827112 |
0.822 |
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| 2010 |
DENMARK SE, STAVENGER RA, WONG K. ChemInform Abstract: The Chemistry of Trichlorosilyl Enolates. Part 4. Lewis Base-Catalyzed, Asymmetric Aldol Additions of Methyl Ketone Enolates. Cheminform. 29: no-no. DOI: 10.1002/chin.199825196 |
0.736 |
|
| 2010 |
DENMARK SE, DIXON JA. ChemInform Abstract: Tandem Inter [4 + 2]/Intra [3 + 2] Cycloadditions of Nitroalkenes. A Versatile Asymmetric Synthesis of Highly Functionalized Aminocyclopentanes. Cheminform. 29: no-no. DOI: 10.1002/chin.199810089 |
0.329 |
|
| 2010 |
DENMARK SE, STAVENGER RA, FAUCHER A, EDWARDS JP. ChemInform Abstract: Cyclopropanation with Diazomethane and Bis(oxazoline)palladium(II) Complexes. Cheminform. 28: no-no. DOI: 10.1002/chin.199738105 |
0.649 |
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| 2010 |
DENMARK SE, HURD AR, SACHA HJ. ChemInform Abstract: Tandem (4 + 2)/(3 + 2) Cycloadditions of Nitroalkenes. Part 13. The Synthesis of (-)-Detoxinine. Cheminform. 28: no-no. DOI: 10.1002/chin.199730186 |
0.341 |
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| 2010 |
DENMARK SE, WONG K, STAVENGER RA. ChemInform Abstract: The Chemistry of Trichlorosilyl Enolates. Part 2. Highly-Selective Asymmetric Aldol Additions of Ketone Enolates. Cheminform. 28: no-no. DOI: 10.1002/chin.199724042 |
0.736 |
|
| 2010 |
DENMARK SE, PARKER DLJ, DIXON JA. ChemInform Abstract: Tandem (4 + 2)/(3 + 2) Cycloadditions of Nitroalkenes. Part 12. Synthesis of (-)-Platynecine. Cheminform. 28: no-no. DOI: 10.1002/chin.199722235 |
0.341 |
|
| 2010 |
DENMARK SE, THORARENSEN A, MIDDLETON DS. ChemInform Abstract: Tandem (4 + 2)/(3 + 2) Cycloadditions of Nitroalkenes. Part 9. Synthesis of (-)-Rosmarinecine. Cheminform. 28: no-no. DOI: 10.1002/chin.199702179 |
0.341 |
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| 2010 |
DENMARK SE, WINTER SBD, SU X, WONG K. ChemInform Abstract: Chemistry of Trichlorosilyl Enolates. Part 1. New Reagents for Catalytic, Asymmetric Aldol Additions. Cheminform. 27: no-no. DOI: 10.1002/chin.199647060 |
0.38 |
|
| 2010 |
DENMARK SE, KIM J. ChemInform Abstract: Asymmetric Michael Addition Reaction of Phosphorus-Stabilized Allyl Anions with Cyclic Enones. Cheminform. 27: no-no. DOI: 10.1002/chin.199614201 |
0.376 |
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| 2010 |
DENMARK SE, NAKAJIMA N, NICAISE OJ, FAUCHER A, EDWARDS JP. ChemInform Abstract: Preparation of Chiral Bisoxazolines: Observations on the Effect of Substituents. Cheminform. 26: no-no. DOI: 10.1002/chin.199549161 |
0.31 |
|
| 2010 |
DENMARK SE, CHEN C. ChemInform Abstract: Enantioselective Synthesis of Alkylidene Cyclohexanes by an Asymmetric Olefination/Cross-Coupling Sequence. Cheminform. 26: no-no. DOI: 10.1002/chin.199549122 |
0.336 |
|
| 2010 |
DENMARK SE, MARCIN LR. ChemInform Abstract: Asymmetric Nitroalkene (4 + 2) Cycloadditions: Enantioselective Synthesis of 3-Substituted and 3,4-Disubstituted Pyrrolidines. Cheminform. 26: no-no. DOI: 10.1002/chin.199539032 |
0.417 |
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| 2010 |
DENMARK SE, FORBES DC, HAYS DS, DEPUE JS, WILDE RG. ChemInform Abstract: Catalytic Epoxidation of Alkenes with Oxone. Cheminform. 26: no-no. DOI: 10.1002/chin.199535068 |
0.373 |
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| 2010 |
DENMARK SE, SCHNUTE ME. ChemInform Abstract: Palladium-Promoted Intramolecular Addition of an Aryl Iodide to a Nitroalkene. Cheminform. 26: no-no. DOI: 10.1002/chin.199533057 |
0.379 |
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| 2010 |
DENMARK SE, CHRISTENSON BL, O'CONNOR SP. ChemInform Abstract: Catalytic Enantioselective Cyclopropanation with Bis(halomethyl)zinc Reagents. Part 2. The Effect of Promoter Structure on Selectivity. Cheminform. 26: no-no. DOI: 10.1002/chin.199530084 |
0.3 |
|
| 2010 |
DENMARK SE, CHRISTENSON BL, COE DM, O'CONNOR SP. ChemInform Abstract: Catalytic Enantioselective Cyclopropanation with Bis(halomethyl)zinc Reagents. Part 1. Optimization of Reaction Protocol. Cheminform. 26: no-no. DOI: 10.1002/chin.199530083 |
0.356 |
|
| 2010 |
DENMARK SE, RIVERA I. ChemInform Abstract: Asymmetric Carboalkoxyalkylidenation with a Chiral Horner-Wadsworth- Emmons Reagent. Cheminform. 26: no-no. DOI: 10.1002/chin.199523070 |
0.337 |
|
| 2010 |
DENMARK SE, THORARENSEN A. ChemInform Abstract: The Tandem Cycloaddition Chemistry of Nitroalkenes. A Novel Synthesis of (-)-Hastanecine. Cheminform. 26: no-no. DOI: 10.1002/chin.199514262 |
0.344 |
|
| 2010 |
HABERMAS KL, DENMARK SE, JONES TK. ChemInform Abstract: The Nazarov cyclization Cheminform. 26: no-no. DOI: 10.1002/chin.199509264 |
0.312 |
|
| 2010 |
DENMARK SE, SCHNUTE ME. ChemInform Abstract: Nitroalkene (4 + 2) Cycloadditions with 2-(Acyloxy)vinyl Ethers. Stereoselective Synthesis of 3-Hydroxy-4-substituted-pyrrolidines. Cheminform. 26: no-no. DOI: 10.1002/chin.199506167 |
0.4 |
|
| 2010 |
DENMARK SE, MARCIN LR. ChemInform Abstract: Nitroalkene (4 + 2)Cycloaddition as a General and Stereoselective Route to the Synthesis of 3,3- and 3,4-Disubstituted Pyrrolidines. Cheminform. 24: no-no. DOI: 10.1002/chin.199345224 |
0.345 |
|
| 2010 |
DENMARK SE, CHEN C. ChemInform Abstract: Electrophilic Activation of the Horner-Wadsworth-Emmons-Wittig Reaction: Highly Selective Synthesis of Dissymmetric Olefins. Cheminform. 24: no-no. DOI: 10.1002/chin.199317099 |
0.388 |
|
| 2010 |
DENMARK SE, KESLER BS, MOON Y. ChemInform Abstract: Inter- and Intramolecular (4 + 2)Cycloadditions of Nitroalkenes with Olefins. 2-Nitrostyrenes. Cheminform. 24: no-no. DOI: 10.1002/chin.199305201 |
0.369 |
|
| 2010 |
DENMARK SE, KIM J. ChemInform Abstract: A Diastereoselective Synthesis of (dl)-1,3-Diphenyl-1,3- propanediamines. Cheminform. 23: no-no. DOI: 10.1002/chin.199230114 |
0.319 |
|
| 2010 |
DENMARK SE, CHATANI N, PANSARE SV. ChemInform Abstract: Asymmetric Electrophilic Amination of Chiral Phosphorus-Stabilized Anions. Cheminform. 23: no-no. DOI: 10.1002/chin.199230045 |
0.676 |
|
| 2010 |
DENMARK SE, ALMSTEAD NG. ChemInform Abstract: On the Stereoselective Opening of Achiral Dioxane Acetals. Cheminform. 23: no-no. DOI: 10.1002/chin.199216076 |
0.316 |
|
| 2010 |
DENMARK SE, ALMSTEAD NG. ChemInform Abstract: On the Stereoselective Opening of Chiral Dioxane Acetals. Nucleophile Dependence. Cheminform. 23: no-no. DOI: 10.1002/chin.199213095 |
0.353 |
|
| 2010 |
DENMARK SE, ALMSTEAD NG. ChemInform Abstract: Studies on the Mechanism and Origin of Stereoselective Opening of Chiral Dioxane Acetals. Cheminform. 23: no-no. DOI: 10.1002/chin.199205081 |
0.304 |
|
| 2010 |
DENMARK SE, DOROW RL. ChemInform Abstract: Stereoselective Alkylations of Chiral, Phosphorus-Stabilized Benzylic Carbanions. Cheminform. 22: no-no. DOI: 10.1002/chin.199113213 |
0.313 |
|
| 2010 |
DENMARK SE, MOON Y, CRAMER CJ, DAPPEN MS, SENANAYAKE CBW. ChemInform Abstract: Intramolecular (4 + 2) Cycloadditions of Nitroalkenes with Olefins. Part 2. Cheminform. 22: no-no. DOI: 10.1002/chin.199107069 |
0.559 |
|
| 2010 |
Denmark S, Liu J. Kreuzkupplungen von Organosiliciumverbindungen in der Naturstoffsynthese Angewandte Chemie. 122: 3040-3049. DOI: 10.1002/Ange.200905657 |
0.477 |
|
| 2009 |
Denmark SE, Baiazitov RY, Nguyen ST. Tandem double intramolecular [4+2]/[3+2] cycloadditions of nitroalkenes: construction of the pentacyclic core structure of daphnilactone B. Tetrahedron. 65: 6535-6548. PMID 22180670 DOI: 10.1016/J.Tet.2009.05.060 |
0.788 |
|
| 2009 |
Denmark SE, Liu JH, Muhuhi JM. Total syntheses of isodomoic acids G and H. Journal of the American Chemical Society. 131: 14188-9. PMID 19807173 DOI: 10.1021/Ja9063475 |
0.632 |
|
| 2009 |
Denmark SE, Baird JD. Preparation of 2,3-Disubstituted Indoles by Sequential Larock Heteroannulation and Silicon-Based Cross-Coupling Reactions. Tetrahedron. 65: 3120-3129. PMID 19784400 DOI: 10.1016/J.Tet.2008.10.043 |
0.714 |
|
| 2009 |
Denmark SE, Eklov BM, Yao PJ, Eastgate MD. On the mechanism of Lewis base catalyzed aldol addition reactions: kinetic and spectroscopic investigations using rapid-injection NMR. Journal of the American Chemical Society. 131: 11770-87. PMID 19642696 DOI: 10.1021/Ja902474J |
0.454 |
|
| 2009 |
Denmark SE. The interplay of invention, discovery, development, and application in organic synthetic methodology: a case study. The Journal of Organic Chemistry. 74: 2915-27. PMID 19278233 DOI: 10.1021/Jo900032X |
0.465 |
|
| 2009 |
Denmark SE, Collins WR, Cullen MD. Observation of direct sulfenium and selenenium group transfer from thiiranium and seleniranium ions to alkenes. Journal of the American Chemical Society. 131: 3490-2. PMID 19227982 DOI: 10.1021/Ja900187Y |
0.625 |
|
| 2009 |
Denmark SE, Smith RC, Chang WT, Muhuhi JM. Cross-coupling reactions of aromatic and heteroaromatic silanolates with aromatic and heteroaromatic halides. Journal of the American Chemical Society. 131: 3104-18. PMID 19199785 DOI: 10.1021/Ja8091449 |
0.682 |
|
| 2009 |
Denmark SE, Nguyen ST. Catalytic, nucleophilic allylation of aldehydes with allyl acetate. Organic Letters. 11: 781-4. PMID 19175354 DOI: 10.1021/Ol8028725 |
0.476 |
|
| 2009 |
Denmark SE, Butler CR. Palladium- (and nickel-) catalyzed vinylation of aryl halides. Chemical Communications (Cambridge, England). 20-33. PMID 19081992 DOI: 10.1039/B809676G |
0.561 |
|
| 2009 |
Denmark SE, Smith RC, Chang W-T, Muhuhi JM. Cross-Coupling of Silanolates with Aromatic Halides Synfacts. 2009: 547-547. DOI: 10.1055/S-0028-1088184 |
0.362 |
|
| 2009 |
Denmark SE, Almstead NG. Stereochemical studies on the addition of allylsilanes to aldehydes. The SE' component Journal of the Mexican Chemical Society. 53: 174-192. DOI: 10.1021/Jo00097A008 |
0.373 |
|
| 2009 |
Denmark SE, Smith RC, Chang WT, Muhuhi JM. ChemInform Abstract: Cross-Coupling Reactions of Aromatic and Heteroaromatic Silanolates with Aromatic and Heteroaromatic Halides. Cheminform. 40. DOI: 10.1002/chin.200927074 |
0.619 |
|
| 2009 |
Denmark SE, Nguyen ST. ChemInform Abstract: Catalytic, Nucleophilic Allylation of Aldehydes with Allyl Acetate. Cheminform. 40. DOI: 10.1002/chin.200925060 |
0.45 |
|
| 2009 |
Denmark SE, Werner NS. ChemInform Abstract: Cross-Coupling of Aromatic Bromides with Allylic Silanolate Salts. Cheminform. 40. DOI: 10.1002/chin.200918064 |
0.732 |
|
| 2009 |
Denmark SE, Butler CR. ChemInform Abstract: Palladium- (and Nickel-) Catalyzed Vinylation of Aryl Halides Cheminform. 40. DOI: 10.1002/chin.200913235 |
0.596 |
|
| 2009 |
Denmark SE, Nguyen ST, Baiazitov RY. ChemInform Abstract: Asymmetric Synthesis of the ABCD Ring System of Daphnilactone B via a Tandem, Double Intramolecular, [4 + 2]/[3 + 2] Cycloaddition Strategy. Cheminform. 40. DOI: 10.1002/chin.200909211 |
0.769 |
|
| 2009 |
Denmark SE, Regens CS. ChemInform Abstract: Palladium-Catalyzed Cross-Coupling Reactions of Organosilanols and Their Salts: Practical Alternatives to Boron- and Tin-Based Methods Cheminform. 40. DOI: 10.1002/chin.200906264 |
0.818 |
|
| 2009 |
Denmark SE, Butler CR. Vinylation with Inexpensive Silicon‐Based Reagents: Preparation of 3‐Vinylquinoline and 4‐Vinylbenzophenone Organic Syntheses. 86: 274-286. DOI: 10.1002/0471264229.Os086.26 |
0.472 |
|
| 2009 |
Denmark SE, Butler CR, Pfaltz A, Woodmansee DH. Vinylation with inexpensive silicon-based reagents: Preparation of 3-vinylquinoline and 4-vinylbenzophenone Organic Syntheses. 86: 274-286. |
0.585 |
|
| 2009 |
Kuethe JT, Beutner GL, Denmark SE, Muhuhi JM. Synthesis of 2-arylindole-4-carboxylic amides: [2(4-Fluorophenyl)-1H-indol- 4-yl]-1-pyrrolidinylmethanone Organic Syntheses. 86: 92-104. |
0.652 |
|
| 2008 |
Denmark SE, Nguyen ST, Baiazitov RY. ASYMMETRIC SYNTHESIS OF THE ABCD RING SYSTEM OF DAPHNILACTONE B VIA A TANDEM, DOUBLE INTRAMOLECULAR, [4+2]/[3+2] CYCLOADDITION STRATEGY. Heterocycles. 76: 143. PMID 20151037 DOI: 10.3987/Com-08-S(N)15 |
0.789 |
|
| 2008 |
Denmark SE, Nakajima N, Stiff CM, Nicaise OJ, Kranz M. Studies on the Bisoxazoline and (-)-Sparteine Mediated Enantioselective Addition of Organolithium Reagents to Imines. Advanced Synthesis & Catalysis. 350: 1023-1045. PMID 19809587 DOI: 10.1002/Adsc.200800017 |
0.463 |
|
| 2008 |
Smith CR, Zhang A, Mans DJ, Rajanbabu TV, Denmark SE, Xie M. (R)-3-METHYL-3-PHENYL-1-PENTENE VIA CATALYTIC ASYMMETRIC HYDROVINYLATION. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 85: 248-266. PMID 19672483 DOI: 10.15227/Orgsyn.085.0248 |
0.556 |
|
| 2008 |
Smith CR, Mans DJ, Rajanbabu TV, Denmark SE, Nguyen ST. (R)-2,2'-BINAPHTHOYL-(S,S)-DI(1-PHENYLETHYL) AMINOPHOSPHINE. SCALABLE PROTOCOLS FOR THE SYNTHESES OF PHOSPHORAMIDITE (FERINGA) LIGANDS. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 85: 238-247. PMID 19655040 DOI: 10.15227/Orgsyn.085.0238 |
0.322 |
|
| 2008 |
Denmark SE, Werner NS. Cross-coupling of aromatic bromides with allylic silanolate salts. Journal of the American Chemical Society. 130: 16382-93. PMID 18998687 DOI: 10.1021/Ja805951J |
0.774 |
|
| 2008 |
Denmark SE, Ares JJ. Stereoselective alkylations of chiral nitro imine and nitro hydrazone dianions. Synthesis of enantiomerically enriched 3-substituted 1-nitrocyclohexenes. The Journal of Organic Chemistry. 73: 9647-56. PMID 18855478 DOI: 10.1021/Jo801790R |
0.471 |
|
| 2008 |
Denmark SE, Regens CS. Palladium-catalyzed cross-coupling reactions of organosilanols and their salts: practical alternatives to boron- and tin-based methods. Accounts of Chemical Research. 41: 1486-99. PMID 18681465 DOI: 10.1021/Ar800037P |
0.83 |
|
| 2008 |
Denmark SE, Chung WJ. Lewis base activation of Lewis acids: catalytic, enantioselective addition of glycolate-derived silyl ketene acetals to aldehydes. The Journal of Organic Chemistry. 73: 4582-95. PMID 18505296 DOI: 10.1021/Jo8006539 |
0.585 |
|
| 2008 |
Denmark SE, Butler CR. Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols. Journal of the American Chemical Society. 130: 3690-704. PMID 18303892 DOI: 10.1021/Ja7100888 |
0.623 |
|
| 2008 |
Denmark SE, Beutner GL. Lewis base catalysis in organic synthesis. Angewandte Chemie (International Ed. in English). 47: 1560-638. PMID 18236505 DOI: 10.1002/Anie.200604943 |
0.71 |
|
| 2008 |
Denmark SE, Chung WJ. Lewis base activation of Lewis acids: catalytic enantioselective glycolate aldol reactions. Angewandte Chemie (International Ed. in English). 47: 1890-2. PMID 18236504 DOI: 10.1002/Anie.200705499 |
0.626 |
|
| 2008 |
Denmark SE, Baird JD, Regens CS. Palladium-catalyzed cross-coupling of five-membered heterocyclic silanolates. The Journal of Organic Chemistry. 73: 1440-55. PMID 18205384 DOI: 10.1021/Jo7023784 |
0.828 |
|
| 2008 |
Denmark SE, Lee W. Investigations into transition-state geometry in the Mukaiyama directed aldol reaction. Chemistry, An Asian Journal. 3: 327-41. PMID 18022982 DOI: 10.1002/Asia.200700300 |
0.402 |
|
| 2008 |
Denmark SE. Asymmetrie catalysis with Chiral Lewis bases: A new frontier in main group chemistry Chimia. 62: 37-40. DOI: 10.2533/Chimia.2008.37 |
0.366 |
|
| 2008 |
Denmark SE, Wilson TW, Burk MT, Heemstra JR. Lewis Acid Mediated Addition of Silyl Ketene Imines to Aldehydes Synfacts. 2008: 175-175. DOI: 10.1055/S-2007-992488 |
0.355 |
|
| 2008 |
Denmark SE, Fujimori S. Chapter 1 Total synthesis of RK-397 Strategies and Tactics in Organic Synthesis. 7: 1-34. DOI: 10.1016/S1874-6004(08)80005-6 |
0.711 |
|
| 2008 |
Kobayashi T, Regens CS, Denmark SE. ChemInform Abstract: Total Syntehsis of Papulacandin D Cheminform. 39. DOI: 10.1002/chin.200847271 |
0.735 |
|
| 2008 |
Denmark SE, Chung W. ChemInform Abstract: Lewis Base Activation of Lewis Acids: Catalytic, Enantioselective Addition of Glycolate-Derived Silyl Ketene Acetals to Aldehydes. Cheminform. 39. DOI: 10.1002/chin.200842045 |
0.334 |
|
| 2008 |
Denmark SE, Nakajima N, Stiff CM, Nicaise OJ, Kranz M. ChemInform Abstract: Bisoxazoline- and (-)-Sparteine-Mediated Enantioselective Addition of Organolithium Reagents to Imines. Cheminform. 39. DOI: 10.1002/chin.200839063 |
0.389 |
|
| 2008 |
Denmark SE, Chung W. ChemInform Abstract: Lewis Base Activation of Lewis Acids: Catalytic Enantioselective Glycolate Aldol Reactions. Cheminform. 39. DOI: 10.1002/chin.200828084 |
0.367 |
|
| 2008 |
Denmark SE, Baird JD, Regens CS. ChemInform Abstract: Palladium-Catalyzed Cross-Coupling of Five-Membered Heterocyclic Silanolates. Cheminform. 39. DOI: 10.1002/chin.200825047 |
0.828 |
|
| 2008 |
Denmark SE, Beutner GL. ChemInform Abstract: Lewis Base Catalysis in Organic Synthesis Cheminform. 39. DOI: 10.1002/chin.200821255 |
0.676 |
|
| 2008 |
Denmark SE, Xie M. ChemInform Abstract: Lewis Acid Promoted Conjugate Addition of Dienol Silyl Ethers to Nitroalkenes: Synthesis of 3-Substituted Azepanes. Cheminform. 39. DOI: 10.1002/chin.200802160 |
0.329 |
|
| 2008 |
Denmark S, Beutner G. Lewis-Base-Katalyse in der organischen Synthese Angewandte Chemie. 120: 1584-1663. DOI: 10.1002/Ange.200604943 |
0.678 |
|
| 2007 |
Denmark SE, Smith RC, Tymonko SA. Phosphine Oxides as Stabilizing Ligands for the Palladium-Catalyzed Cross-Coupling of Potassium Aryldimethylsilanolates. Tetrahedron. 63: 5730-5738. PMID 23162169 DOI: 10.1016/J.Tet.2007.02.017 |
0.831 |
|
| 2007 |
Kohnen AL, Danheiser RL, Denmark SE, Liu X. SYNTHESIS OF TERMINAL 1,3-DIYNES VIA SONOGASHIRA COUPLING OF VINYLIDENE CHLORIDE FOLLOWED BY ELIMINATION. PREPARATION OF 1,3-DECADIYNE. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 84: 77-87. PMID 20628544 DOI: 10.15227/Orgsyn.084.0077 |
0.403 |
|
| 2007 |
Denmark SE, Ahmad M. Carbonylative ring opening of terminal epoxides at atmospheric pressure. The Journal of Organic Chemistry. 72: 9630-4. PMID 17988145 DOI: 10.1021/Jo7014455 |
0.407 |
|
| 2007 |
Denmark SE, Wilson TW, Burk MT, Heemstra JR. Enantioselective construction of quaternary stereogenic carbons by the Lewis base catalyzed additions of silyl ketene imines to aldehydes. Journal of the American Chemical Society. 129: 14864-5. PMID 17988135 DOI: 10.1021/Ja077134Y |
0.842 |
|
| 2007 |
Denmark SE, Collins WR. Lewis base activation of Lewis acids: development of a Lewis base catalyzed selenolactonization. Organic Letters. 9: 3801-4. PMID 17705396 DOI: 10.1021/Ol701617D |
0.701 |
|
| 2007 |
Denmark SE, Xie M. Lewis acid-promoted conjugate addition of dienol silyl ethers to nitroalkenes: synthesis of 3-substituted azepanes. The Journal of Organic Chemistry. 72: 7050-3. PMID 17676807 DOI: 10.1021/Jo071126I |
0.526 |
|
| 2007 |
Denmark SE, Heemstra JR. Lewis base activation of Lewis acids: catalytic, enantioselective vinylogous aldol addition reactions. The Journal of Organic Chemistry. 72: 5668-88. PMID 17583959 DOI: 10.1021/Jo070638U |
0.827 |
|
| 2007 |
Denmark SE, Liu JH. Sequential silylcarbocyclization/silicon-based cross-coupling reactions. Journal of the American Chemical Society. 129: 3737-44. PMID 17335205 DOI: 10.1021/Ja067854P |
0.688 |
|
| 2007 |
Denmark SE, Regens CS, Kobayashi T. Total synthesis of papulacandin D. Journal of the American Chemical Society. 129: 2774-6. PMID 17305346 DOI: 10.1021/Ja070071Z |
0.77 |
|
| 2007 |
Zhang W, Cho HM, Moore JS, Denmark SE, Butler CR. Preparation of a Carbazole‐Based Macrocycle Via Precipitation‐Driven Alkyne Metathesis Organic Syntheses. 177-191. DOI: 10.15227/Orgsyn.084.0177 |
0.425 |
|
| 2007 |
Denmark SE, Barsanti PA, Beutner GL, Wilson TW. Enantioselective Lewis Acid-Lewis Base Ring Opening of Epoxides Synfacts. 2007: 614-614. DOI: 10.1055/S-2007-968504 |
0.375 |
|
| 2007 |
Denmark SE, Ghosh SK. Unexpected ambidoselectivity in crossed-aldol reactions of α-oxy aldehyde trichlorosilyl enolates Tetrahedron. 63: 8636-8644. DOI: 10.1016/J.Tet.2007.04.009 |
0.466 |
|
| 2007 |
Denmark SE, Barsanti PA, Beutner GL, Wilson TW. Enantioselective ring opening of epoxides with silicon tetrachloride in the presence of a chiral lewis base: Mechanism studies Advanced Synthesis and Catalysis. 349: 566-582. DOI: 10.1002/Adsc.200600551 |
0.843 |
|
| 2006 |
Denmark SE, Kallemeyn JM. Stereospecific palladium-catalyzed cross-coupling of (E)- and (Z)-alkenylsilanolates with aryl chlorides. Journal of the American Chemical Society. 128: 15958-9. PMID 17165708 DOI: 10.1021/Ja065988X |
0.82 |
|
| 2006 |
Denmark SE, Neuville L, Christy ME, Tymonko SA. A qualitative examination of the effects of silicon substituents on the efficiency of cross-coupling reactions. The Journal of Organic Chemistry. 71: 8500-9. PMID 17064026 DOI: 10.1021/Jo061481T |
0.816 |
|
| 2006 |
Denmark SE, Edwards MG. On the mechanism of the selenolactonization reaction with selenenyl halides. The Journal of Organic Chemistry. 71: 7293-306. PMID 16958523 DOI: 10.1021/Jo0610457 |
0.633 |
|
| 2006 |
Denmark SE. Organic chemistry: catalysts break symmetry. Nature. 443: 40-1. PMID 16957721 DOI: 10.1038/443040B |
0.408 |
|
| 2006 |
Denmark SE, Montgomery JI, Kramps LA. Synthesis, X-ray crystallography, and computational analysis of 1-azafenestranes. Journal of the American Chemical Society. 128: 11620-30. PMID 16939287 DOI: 10.1021/Ja0632759 |
0.59 |
|
| 2006 |
Denmark SE, Montgomery JI. A general synthesis of N-vinyl nitrones. The Journal of Organic Chemistry. 71: 6211-20. PMID 16872207 DOI: 10.1021/Jo060975N |
0.591 |
|
| 2006 |
Denmark SE, Chung WJ. Lewis base catalyzed addition of trimethylsilyl cyanide to aldehydes. The Journal of Organic Chemistry. 71: 4002-5. PMID 16674085 DOI: 10.1021/Jo060153Q |
0.647 |
|
| 2006 |
Denmark SE, Pham SM, Stavenger RA, Su X, Wong KT, Nishigaichi Y. Chiral phosphoramide-catalyzed aldol additions of ketone trichlorosilyl enolates. Mechanistic aspects. The Journal of Organic Chemistry. 71: 3904-22. PMID 16674067 DOI: 10.1021/Jo060243V |
0.794 |
|
| 2006 |
Denmark SE, Baird JD. Palladium-catalyzed cross-coupling reactions of silanolates: a paradigm shift in silicon-based cross-coupling reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 4954-63. PMID 16671045 DOI: 10.1002/Chem.200600034 |
0.676 |
|
| 2006 |
Denmark SE, Venkatraman S. On the mechanism of the Skraup-Doebner-Von Miller quinoline synthesis. The Journal of Organic Chemistry. 71: 1668-76. PMID 16468822 DOI: 10.1021/Jo052410H |
0.364 |
|
| 2006 |
Denmark SE, Fu J, Lawler MJ. Chiral phosphoramide-catalyzed enantioselective addition of allylic trichlorosilanes to aldehydes. Preparative studies with bidentate phosphorus-based amides. The Journal of Organic Chemistry. 71: 1523-36. PMID 16468801 DOI: 10.1021/Jo052203H |
0.668 |
|
| 2006 |
Denmark SE, Fu J, Coe DM, Su X, Pratt NE, Griedel BD. Chiral phosphoramide-catalyzed enantioselective addition of allylic trichlorosilanes to aldehydes. Preparative and mechanistic studies with monodentate phosphorus-based amides. The Journal of Organic Chemistry. 71: 1513-22. PMID 16468800 DOI: 10.1021/Jo052202P |
0.658 |
|
| 2006 |
Denmark SE, Baird JD. Palladium-catalyzed cross-coupling reactions of heterocyclic silanolates with substituted aryl iodides and bromides. Organic Letters. 8: 793-5. PMID 16468769 DOI: 10.1021/Ol053165R |
0.678 |
|
| 2006 |
Denmark SE, Heemstra JR. Lewis base activation of Lewis acids. Vinylogous aldol addition reactions of conjugated N,O-silyl ketene acetals to aldehydes. Journal of the American Chemical Society. 128: 1038-9. PMID 16433495 DOI: 10.1021/Ja056747C |
0.825 |
|
| 2006 |
Denmark SE, Baiazitov RY. Tandem double-intramolecular [4+2]/[3+2] cycloadditions of nitroalkenes. Studies toward a total synthesis of daphnilactone B: piperidine ring construction. The Journal of Organic Chemistry. 71: 593-605. PMID 16408969 DOI: 10.1021/Jo052001L |
0.777 |
|
| 2006 |
Denmark SE, Butler CR. Vinylation of aryl bromides using an inexpensive vinylpolysiloxane. Organic Letters. 8: 63-6. PMID 16381568 DOI: 10.1021/Ol052517R |
0.619 |
|
| 2006 |
Denmark SE, Smith RC. Reduction of allylpalladium(II)chloride dimer by formation of allyloxysilanes Synlett. 2921-2928. DOI: 10.1055/S-2006-951516 |
0.563 |
|
| 2006 |
Denmark SE, Baiazitov RY. Intramolecular [4+2] Cycloaddition of Nitroalkenes Synfacts. 2006: 135-135. DOI: 10.1055/S-2005-924781 |
0.808 |
|
| 2006 |
Denmark SE, Fan Y. Preparation of chiral bipyridine bis-N-oxides by oxidative dimerization of chiral pyridine N-oxides Tetrahedron Asymmetry. 17: 687-707. DOI: 10.1016/J.Tetasy.2005.12.039 |
0.319 |
|
| 2006 |
Denmark SE, Cottell JJ. A tandem, nitroalkene conjugate addition/[3+2] cycloaddition approach to the synthesis of the pentacyclic core of (±)-scandine Advanced Synthesis and Catalysis. 348: 2397-2402. DOI: 10.1002/Adsc.200600301 |
0.836 |
|
| 2006 |
Denmark SE, Fu J, Lawler MJ. (R,R)‐2,2′‐Bispyrrolidine and (S,S)‐2,2′‐Bispyrrolidine: Useful Ligands for Asymmetric Synthesis Organic Syntheses. 83: 121-130. DOI: 10.1002/0471264229.Os083.17 |
0.326 |
|
| 2006 |
Denmark SE, Fu J, Lawler MJ. (R,R)-2,2′-bispyrrolidine and (S,S)-2,2′-bispyrrolidine: Useful ligands for asymmetric synthesis Organic Syntheses. 83: 121-130. |
0.431 |
|
| 2005 |
Denmark SE, Fujimori S, Pham SM. Lewis base catalyzed aldol additions of chiral trichlorosilyl enolates and silyl enol ethers. The Journal of Organic Chemistry. 70: 10823-40. PMID 16356006 DOI: 10.1021/Jo051930+ |
0.771 |
|
| 2005 |
Denmark SE, Bui T. Mechanistic insights into the chiral phosphoramide-catalyzed, enantioselective crossed-aldol reactions of aldehydes. The Journal of Organic Chemistry. 70: 10393-9. PMID 16323849 DOI: 10.1021/Jo051680X |
0.66 |
|
| 2005 |
Denmark SE, Baiazitov RY. Intramolecular [4 + 2] cycloaddition of nitroalkenes for construction of vicinal quaternary stereocenters. Organic Letters. 7: 5617-20. PMID 16321005 DOI: 10.1021/Ol052316N |
0.777 |
|
| 2005 |
Denmark SE, Bui T. Lewis base catalyzed enantioselective aldol addition of acetaldehyde-derived silyl enol ether to aldehydes. The Journal of Organic Chemistry. 70: 10190-3. PMID 16292871 DOI: 10.1021/Jo0517500 |
0.7 |
|
| 2005 |
Denmark SE, Fan Y. Catalytic, enantioselective alpha-additions of isocyanides: Lewis base catalyzed Passerini-type reactions. The Journal of Organic Chemistry. 70: 9667-76. PMID 16292793 DOI: 10.1021/Jo050549M |
0.595 |
|
| 2005 |
Denmark SE, Fujimori S. Total synthesis of RK-397. Journal of the American Chemical Society. 127: 8971-3. PMID 15969572 DOI: 10.1021/Ja052226D |
0.688 |
|
| 2005 |
Denmark SE, Fan Y, Eastgate MD. Lewis base catalyzed, enantioselective aldol addition of methyl trichlorosilyl ketene acetal to ketones. The Journal of Organic Chemistry. 70: 5235-48. PMID 15960528 DOI: 10.1021/Jo0506276 |
0.596 |
|
| 2005 |
Denmark SE, Heemstra JR, Beutner GL. Catalytic, enantioselective, vinylogous aldol reactions. Angewandte Chemie (International Ed. in English). 44: 4682-98. PMID 15940727 DOI: 10.1002/Anie.200462338 |
0.829 |
|
| 2005 |
Denmark SE, Tymonko SA. Sequential cross-coupling of 1,4-bissilylbutadienes: synthesis of unsymmetrical 1,4-disubstituted 1,3-butadienes. Journal of the American Chemical Society. 127: 8004-5. PMID 15926811 DOI: 10.1021/Ja0518373 |
0.826 |
|
| 2005 |
Denmark SE, Montgomery JI. Synthesis of cis,cis,cis,cis-[5.5.5.4]-1-azafenestrane with discovery of an unexpected dyotropic rearrangement. Angewandte Chemie (International Ed. in English). 44: 3732-6. PMID 15887203 DOI: 10.1002/Anie.200500367 |
0.498 |
|
| 2005 |
Denmark SE, Kallemeyn JM. Synthesis of 3,4,5-trisubstituted isoxazoles via sequential [3 + 2] cycloaddition/silicon-based cross-coupling reactions. The Journal of Organic Chemistry. 70: 2839-42. PMID 15787583 DOI: 10.1021/Jo047755Z |
0.83 |
|
| 2005 |
Denmark SE, Beutner GL, Wynn T, Eastgate MD. Lewis base activation of Lewis acids: catalytic, enantioselective addition of silyl ketene acetals to aldehydes. Journal of the American Chemical Society. 127: 3774-89. PMID 15771512 DOI: 10.1021/Ja047339W |
0.755 |
|
| 2005 |
Rathore R, Burns CL, Denmark SE, Fujimori S. Preparation of hexakis(4-Bromophenyl)benzene (HBB) [1,1':2',1''-Terphenyl, 4,4''-dibromo-3',4',5',6'-tetrakis(4-Bromophenyl)-] Organic Syntheses. 82: 30-33. DOI: 10.15227/Orgsyn.082.0030 |
0.601 |
|
| 2005 |
Rathore R, Burns CL, Deselnicu MI, Denmark SE, Bui T. Preparation of 1,4: 5,8-dimethano-1,2,3,4,5,6,7,8-octahydro-9,10-dimethoxyanthracenium hexachloroantimonate (4+•SbCl6 -): A highly robust radical-cation salt: [1,4:5,8-dimethanoanthracene, 1,2,3,4,5,6,7,8-octahydro-9,10-dimethoxy-, radical ion(1+), hexachloroantimonate(1-)] Organic Syntheses. 82: 1-9. DOI: 10.15227/Orgsyn.082.0001 |
0.524 |
|
| 2005 |
Bailey WF, Luderer MR, Mealy MJ, Punzalan ER, Denmark SE, Macneil SL. Generation and cyclization of 5-hexenyllithium: 2-cyclopentylacetophenone: (ethanone, 2-cyclopentyl-1-phenyl-) Organic Syntheses. 81: 121-133. DOI: 10.15227/Orgsyn.081.0121 |
0.359 |
|
| 2005 |
Denmark SE, Wang Z. Platinum catalyzed hydrosilylation and palladium catalyzed cross-coupling: One-pot hydroarylation of 1-heptyne to (E)-1-(1-heptenyl)-4methoxybenzene Organic Syntheses. 81. DOI: 10.15227/Orgsyn.081.0054 |
0.434 |
|
| 2005 |
Denmark SE, Fujimori S. Synthesis of RK-397 Synfacts. 2005: 272-272. DOI: 10.1055/S-2005-921601 |
0.611 |
|
| 2005 |
Denmark SE, Yang SM. Chapter 4 Application of silicon-assisted intramolecular cross-coupling in total synthesis of (+)-brasilenyne Strategies and Tactics in Organic Synthesis. 6: 100-136. DOI: 10.1016/S1874-6004(05)80027-9 |
0.469 |
|
| 2005 |
Denmark SE, Heemstra JR, Beutner GL. Katalytische enantioselektive vinyloge Aldolreaktionen Angewandte Chemie. 117: 4760-4777. DOI: 10.1002/Ange.200462338 |
0.766 |
|
| 2005 |
Denmark SE, Wang Z. Platinum Catalyzed Hydrosilylation and Palladium Catalyzed Cross‐Coupling: One‐Pot Hydroarylation of 1‐Heptyne to (E)‐1‐(1‐Heptenyl)‐4‐methoxybenzene Organic Syntheses. 81: 54-62. DOI: 10.1002/0471264229.Os081.06 |
0.445 |
|
| 2005 |
Denmark SE, Wang Z. Palladium Catalyzed Cross‐Coupling of (Z)‐1‐Heptenyldimethylsilanol with 4‐Iodoanisole: (Z)‐1‐Heptenyl)‐4‐methoxybenzene Organic Syntheses. 81: 42-53. DOI: 10.1002/0471264229.Os081.05 |
0.434 |
|
| 2004 |
Denmark SE, Yang SM. Total synthesis of (+)-brasilenyne. Application of an intramolecular silicon-assisted cross-coupling reaction. Journal of the American Chemical Society. 126: 12432-40. PMID 15453777 DOI: 10.1021/Ja0466863 |
0.502 |
|
| 2004 |
Denmark SE, Baird JD. Palladium-catalyzed cross-coupling reactions of 2-indolyldimethylsilanols with substituted aryl halides. Organic Letters. 6: 3649-52. PMID 15387570 DOI: 10.1021/Ol048328A |
0.692 |
|
| 2004 |
Denmark SE, Sweis RF. Cross-coupling reactions of alkenylsilanolates. Investigation of the mechanism and identification of key intermediates through kinetic analysis. Journal of the American Chemical Society. 126: 4876-82. PMID 15080692 DOI: 10.1021/Ja0372356 |
0.778 |
|
| 2004 |
Denmark SE, Sweis RF, Wehrli D. Fluoride-promoted cross-coupling reactions of alkenylsilanols. Elucidation of the mechanism through spectroscopic and kinetic analysis. Journal of the American Chemical Society. 126: 4865-75. PMID 15080691 DOI: 10.1021/Ja037234D |
0.782 |
|
| 2004 |
Denmark SE, Bui T. Chiral phosphoramide-catalyzed, enantioselective, directed cross-aldol reactions of aldehydes. Proceedings of the National Academy of Sciences of the United States of America. 101: 5439-44. PMID 15067133 DOI: 10.1073/Pnas.0307212101 |
0.699 |
|
| 2004 |
Denmark SE, Heemstra JR. Lewis base activation of Lewis acids: Vinylogous aldol additions of silyl dienol ethers to aldehydes Synlett. 2411-2416. DOI: 10.1055/S-2004-834789 |
0.827 |
|
| 2004 |
Denmark SE, Yang SM. Sequential ring-closing metathesis/Pd-catalyzed, Si-assisted cross-coupling reactions: General synthesis of highly substituted unsaturated alcohols and medium-sized rings containing a 1,3-cis-cis diene unit Tetrahedron. 60: 9695-9708. DOI: 10.1016/J.Tet.2004.06.149 |
0.497 |
|
| 2004 |
Denmark SE, Ober MH. Palladium-catalyzed cross-coupling reactions of substituted aryl(dimethyl)silanols Advanced Synthesis and Catalysis. 346: 1703-1714. DOI: 10.1002/Adsc.200404204 |
0.792 |
|
| 2004 |
Habermas KL, Denmark SE, Jones TK. The Nazarov Cyclization Organic Reactions. DOI: 10.1002/0471264180.Or045.01 |
0.53 |
|
| 2003 |
Tishkov AA, Lesiv AV, Khomutova YA, Strelenko YA, Nesterov ID, Antipin MY, Ioffe SL, Denmark SE. 2-silyloxy-1,2-oxazines, a new type of acetals of conjugated nitroso alkenes. The Journal of Organic Chemistry. 68: 9477-80. PMID 14629175 DOI: 10.1021/Jo034669A |
0.348 |
|
| 2003 |
Denmark SE, Tymonko SA. Cross-coupling of alkynylsilanols with aryl halides promoted by potassium trimethylsilanolate. The Journal of Organic Chemistry. 68: 9151-4. PMID 14604401 DOI: 10.1021/Jo0351771 |
0.829 |
|
| 2003 |
Denmark SE, Gomez L. Tandem double intramolecular [4+2]/[3+2] cycloadditions of nitroalkenes. The fused/bridged mode. The Journal of Organic Chemistry. 68: 8015-24. PMID 14535778 DOI: 10.1021/Jo034853W |
0.374 |
|
| 2003 |
Denmark SE, Kallemeyn JM. Palladium-catalyzed silylation of aryl bromides leading to functionalized aryldimethylsilanols. Organic Letters. 5: 3483-6. PMID 12967305 DOI: 10.1021/Ol035288M |
0.822 |
|
| 2003 |
Denmark SE, Amishiro N. Palladium-catalyzed conjugate addition of organosiloxanes to alpha,beta-unsaturated carbonyl compounds and nitroalkenes. The Journal of Organic Chemistry. 68: 6997-7003. PMID 12946140 DOI: 10.1021/Jo034763R |
0.387 |
|
| 2003 |
Denmark SE, Fu J. Catalytic enantioselective addition of allylic organometallic reagents to aldehydes and ketones. Chemical Reviews. 103: 2763-94. PMID 12914480 DOI: 10.1021/Cr020050H |
0.674 |
|
| 2003 |
Denmark SE, Fan Y. The first catalytic, asymmetric alpha-additions of isocyanides. Lewis-base-catalyzed, enantioselective Passerini-type reactions. Journal of the American Chemical Society. 125: 7825-7. PMID 12823000 DOI: 10.1021/Ja035410C |
0.564 |
|
| 2003 |
Denmark SE, Beutner GL. Lewis base activation of Lewis acids. Vinylogous aldol reactions. Journal of the American Chemical Society. 125: 7800-1. PMID 12822988 DOI: 10.1021/Ja035448P |
0.766 |
|
| 2003 |
Denmark SE, Kobayashi T. Tandem intramolecular silylformylation and silicon-assisted cross-coupling reactions. synthesis of geometrically defined alpha,beta-unsaturated aldehydes. The Journal of Organic Chemistry. 68: 5153-9. PMID 12816470 DOI: 10.1021/Jo034064E |
0.49 |
|
| 2003 |
Denmark SE, Pham SM. Stereoselective aldol additions of achiral ethyl ketone-derived trichlorosilyl enolates. The Journal of Organic Chemistry. 68: 5045-55. PMID 12816457 DOI: 10.1021/Jo034092X |
0.718 |
|
| 2003 |
Denmark SE, Heemstra JR. Lewis base activation of Lewis acids. Catalytic enantioselective addition of silyl enol ethers of achiral methyl ketones to aldehydes. Organic Letters. 5: 2303-6. PMID 12816434 DOI: 10.1021/Ol034641L |
0.84 |
|
| 2003 |
Denmark SE, Ober MH. Cross-coupling reactions of arylsilanols with substituted aryl halides. Organic Letters. 5: 1357-60. PMID 12688758 DOI: 10.1021/Ol034328J |
0.802 |
|
| 2003 |
Denmark SE, Pan W. Intramolecular syn and anti hydrosilylation and silicon-assisted cross-coupling: highly regio- and stereoselective synthesis of trisubstituted allylic alcohols. Organic Letters. 5: 1119-22. PMID 12659588 DOI: 10.1021/Ol0342002 |
0.49 |
|
| 2003 |
Denmark SE, Fu J. Understanding the correlation of structure and selectivity in the chiral-phosphoramide-catalyzed enantioselective allylation reactions: solution and solid-state structural studies of bisphosphoramide.SnCl(4) complexes. Journal of the American Chemical Society. 125: 2208-16. PMID 12590549 DOI: 10.1021/Ja021280G |
0.525 |
|
| 2003 |
Denmark SE, Fu J. Catalytic enantioselective allylation with chiral Lewis bases. Chemical Communications (Cambridge, England). 167-70. PMID 12585378 DOI: 10.1039/B208065F |
0.635 |
|
| 2003 |
Danheiser RL, Okamoto I, Lawlor MD, Lee TW, Denmark SE, Ober MH. Generation and [2+2] cycloadditions of thio-substituted ketenes: trans-1-(4-methoxyphenyl)-4-phenyl-3-(phenylthio)azetidin-2-one [(2-azetidinone, 1-(4-methoxyphenyl)-4-phenyl-3-(phenylthio)-, trans-)] Organic Syntheses. 80: 160-171. DOI: 10.15227/Orgsyn.080.0160 |
0.746 |
|
| 2003 |
Denmark SE, Ober MH. Organosilicon Reagents: Synthesis and Application to Palladium-Catalyzed Cross-Coupling Reactions Aldrichimica Acta. 36: 75-85. DOI: 10.1002/chin.200436264 |
0.777 |
|
| 2003 |
Kitamura M, Oka H, Suga S, Noyori R, Kaelin DE, Martin SF, Beutner GL, Denmark SE. Catalytic Enantioselective Addition of Dialkylzincs to Aldehydes Using (2S)‐(−)‐3‐exo‐(Dimethylamino)Isoborneol [(2S)‐DAIB]: (S)‐1‐Phenyl‐1‐Propanol Organic Syntheses. 79: 139-145. DOI: 10.1002/0471264180.Os079.17 |
0.402 |
|
| 2003 |
Denmark SE, Marcin LR, Schnute ME, Thorarensen A. (R)‐(−)‐2,2‐Diphenylcyclopentanol Organic Syntheses. 74: 33-33. DOI: 10.1002/0471264180.Os074.04 |
0.465 |
|
| 2002 |
Denmark SE, Sweis RF. Cross-coupling reactions of organosilicon compounds: new concepts and recent advances. Chemical & Pharmaceutical Bulletin. 50: 1531-41. PMID 12499586 DOI: 10.1248/Cpb.50.1531 |
0.776 |
|
| 2002 |
Denmark SE, Yang SM. Intramolecular silicon-assisted cross-coupling: total synthesis of (+)-brasilenyne. Journal of the American Chemical Society. 124: 15196-7. PMID 12487594 DOI: 10.1021/Ja028936Q |
0.476 |
|
| 2002 |
Denmark SE, Pan W. Intramolecular anti-hydrosilylation and silicon-assisted cross-coupling: highly regio- and stereoselective synthesis of trisubstituted homoallylic alcohols. Organic Letters. 4: 4163-6. PMID 12423112 DOI: 10.1002/chin.200313081 |
0.383 |
|
| 2002 |
Denmark SE, Wynn T, Beutner GL. Lewis base activation of lewis acids. Addition of silyl ketene acetals to aldehydes. Journal of the American Chemical Society. 124: 13405-7. PMID 12418891 DOI: 10.1021/Ja0282947 |
0.762 |
|
| 2002 |
Denmark SE, Kramps LA, Montgomery JI. Synthesis of cis,cis,cis,cis-[5.5.5.5]-1-azafenestrane. Angewandte Chemie (International Ed. in English). 41: 4122-5. PMID 12412102 DOI: 10.1002/1521-3773(20021104)41:21<4122::Aid-Anie4122>3.0.Co;2-W |
0.493 |
|
| 2002 |
Denmark SE, Sweis RF. Design and implementation of new, silicon-based, cross-coupling reactions: importance of silicon-oxygen bonds. Accounts of Chemical Research. 35: 835-46. PMID 12379136 DOI: 10.1021/Ar020001R |
0.767 |
|
| 2002 |
Denmark SE, Sweis RF. Cross-coupling reactions of alkenylsilanols with fluoroalkylsulfonates. Organic Letters. 4: 3771-4. PMID 12375940 DOI: 10.1021/Ol026900X |
0.779 |
|
| 2002 |
Denmark SE, Fujimori S. The effects of a remote stereogenic center in the Lewis base catalyzed aldol additions of chiral trichlorosilyl enolates. Organic Letters. 4: 3477-80. PMID 12323048 DOI: 10.1021/Ol026594N |
0.696 |
|
| 2002 |
Denmark SE, Fujimori S. Diastereoselective aldol additions of chiral beta-hydroxy ethyl ketone enolates catalyzed by Lewis bases. Organic Letters. 4: 3473-6. PMID 12323047 DOI: 10.1021/Ol026593V |
0.686 |
|
| 2002 |
Denmark SE, Fu J. Asymmetric construction of quaternary centers by enantioselective allylation: application to the synthesis of the serotonin antagonist LY426965. Organic Letters. 4: 1951-3. PMID 12027655 DOI: 10.1021/Ol025971T |
0.653 |
|
| 2002 |
Denmark SE, Matsuhashi H. Chiral fluoro ketones for catalytic asymmetric epoxidation of alkenes with oxone. The Journal of Organic Chemistry. 67: 3479-86. PMID 12003563 DOI: 10.1021/Jo020050H |
0.505 |
|
| 2002 |
Denmark SE, Fan Y. Catalytic, enantioselective aldol additions to ketones. Journal of the American Chemical Society. 124: 4233-5. PMID 11960451 DOI: 10.1021/Ja025670E |
0.615 |
|
| 2002 |
Denmark SE, Yang SM. Intramolecular silicon-assisted cross-coupling reactions: general synthesis of medium-sized rings containing a 1,3-cis-cis diene unit. Journal of the American Chemical Society. 124: 2102-3. PMID 11878949 DOI: 10.1021/Ja0178158 |
0.454 |
|
| 2002 |
Denmark SE, Dorow RL. Stereospecific cleavage of carbon-phosphorus bonds: stereochemical course of the phosphinoyl curtius (Harger) reaction. Chirality. 14: 241-57. PMID 11835571 DOI: 10.1002/Chir.10062 |
0.333 |
|
| 2002 |
Denmark SE, Gomez L. Inter- and intramolecular [4+2] cycloaddition of nitroalkenes with allenylsilanes. A case of unexpected regioselectivity Heterocycles. 58: 129-136. DOI: 10.3987/Com-02-S(M)58 |
0.41 |
|
| 2002 |
Ronsheim MD, Hilgenkamp RK, Zercher CK, Denmark SE, Beutner GL. Formation of γ-keto esters from -keto esters: Methyl 5.5-dimethyl-4-oxohexanoate Organic Syntheses. 79: 146-152. DOI: 10.15227/Orgsyn.079.0146 |
0.679 |
|
| 2002 |
Kitamura M, Oka H, Suga S, Noyori R, Kaelin DE, Martin SF, Beutner GL, Denmark SE. Catalytic enantioselective addition of dialkylzincs to aldehydes using (2s)-(-)-3-exo-(dimethylamino)isoborneol [(2S)DAIB]: (S)-1-phenyl-1-propanol Organic Syntheses. 79: 139-145. DOI: 10.15227/Orgsyn.079.0139 |
0.669 |
|
| 2002 |
Gonzalez J, Aurigemma C, Truesdale L, Denmark SE, Tymonko SA, Cottell JJ, Gomez L. Synthesis of (+)-(1S,2R)- AND (í)-(1R,2S)-trans-2-phenylcyclohexanol via sharpless asymmetric dihydroxylation (AD): [Cyclohexanol, 2-phenyl-, (1s-trans)- and cyclohexanol, 2-phenyl-, (1r-trans)-] Organic Syntheses. 79. DOI: 10.15227/Orgsyn.079.0093 |
0.778 |
|
| 2002 |
Denmark SE, Pan W. Efficient and stereoselective cross-coupling with highly substituted alkenylsilanols Journal of Organometallic Chemistry. 653: 98-104. DOI: 10.1016/S0022-328X(02)01268-8 |
0.532 |
|
| 2002 |
Denmark SE, Juhl M. Tandem inter [4+2]/intra [3+2] cycloadditions of nitroalkenes. Application to the synthesis of aminocarbasugars Helvetica Chimica Acta. 85: 3712-3736. DOI: 10.1002/1522-2675(200211)85:11<3712::Aid-Hlca3712>3.0.Co;2-5 |
0.442 |
|
| 2002 |
Gonzalez J, Aurigemma C, Truesdale L, Denmark SE, Tymonko SA, Cottell JJ, Gomez L. Synthesis of (+)-(1S,2R)- and (-)-(! R,2S)-trans-2-phenylcyclohexanol via sharpless asymmetric dihydroxylation (AD) Organic Syntheses. 79: 93-102. |
0.772 |
|
| 2002 |
Christopher McWilliams J, Fleitz FJ, Zheng N, Armstrong JD, Denmark SE, Sweis RF. Preparation of n-butyl 4-chlorophenyl sulfide Organic Syntheses. 79: 43-49. |
0.688 |
|
| 2001 |
Denmark SE, Wynn T, Jellerichs BG. Beneficial Effect of ortho-Methoxy Groups in the Asymmetric Ring Opening of meso Epoxides with Silicon Tetrachloride Catalyzed by Chiral ortho-Methoxyphenyldiazaphosphonamide Lewis Bases Response to the Communication by G. Buono et al. Angewandte Chemie (International Ed. in English). 40: 2255-2256. PMID 29711813 DOI: 10.1002/1521-3773(20010618)40:12<2255::Aid-Anie2255>3.0.Co;2-3 |
0.367 |
|
| 2001 |
Denmark SE, Ghosh SK. The First Catalytic, Diastereoselective, and Enantioselective Crossed-Aldol Reactions of Aldehydes We are grateful to the National Science Foundation for generous financial support (NSF CHE 9803124). Angewandte Chemie (International Ed. in English). 40: 4759-4762. PMID 12404409 DOI: 10.1002/1521-3773(20011217)40:24<4759::Aid-Anie4759>3.0.Co;2-G |
0.814 |
|
| 2001 |
Denmark SE, Fu J. Catalytic, enantioselective addition of substituted allylic trichlorosilanes using a rationally-designed 2,2'-bispyrrolidine-based bisphosphoramide. Journal of the American Chemical Society. 123: 9488-9. PMID 11562250 DOI: 10.1021/Ja016552E |
0.586 |
|
| 2001 |
Denmark SE, Gomez L. Tandem double intramolecular [4 + 2]/[3 + 2] cycloadditions of nitroalkenes. Organic Letters. 3: 2907-10. PMID 11529787 DOI: 10.1021/Ol016385N |
0.423 |
|
| 2001 |
Denmark SE, Pham SM. Highly diastereoselective aldol additions of a chiral ethyl ketone enolate under Lewis base catalysis. Organic Letters. 3: 2201-4. PMID 11440579 DOI: 10.1021/Ol0160497 |
0.7 |
|
| 2001 |
Denmark SE, Pan W. Intramolecular hydrosilylation and silicon-assisted cross-coupling: an efficient route to trisubstituted homoallylic alcohols. Organic Letters. 3: 61-4. PMID 11429872 DOI: 10.1021/Ol006769Y |
0.408 |
|
| 2001 |
Denmark SE, Sweis RF. Fluoride-free cross-coupling of organosilanols. Journal of the American Chemical Society. 123: 6439-40. PMID 11427080 DOI: 10.1021/Ja016021Q |
0.731 |
|
| 2001 |
Denmark SE, Wynn T. Lewis base activation of Lewis acids: catalytic enantioselective allylation and propargylation of aldehydes. Journal of the American Chemical Society. 123: 6199-200. PMID 11414863 DOI: 10.1021/Ja016017E |
0.423 |
|
| 2001 |
Denmark SE, Yang SM. Sequential ring-closing metathesis and silicon-assisted cross-coupling reactions: stereocontrolled synthesis of highly substituted unsaturated alcohols. Organic Letters. 3: 1749-52. PMID 11405702 DOI: 10.1021/Ol015950J |
0.494 |
|
| 2001 |
Denmark SE, Cottell JJ. Synthesis of (+)-1-epiaustraline. The Journal of Organic Chemistry. 66: 4276-84. PMID 11397164 DOI: 10.1021/Jo0101510 |
0.842 |
|
| 2001 |
Denmark SE, Wang Z. Highly stereoselective hydrocarbation of terminal alkynes via Pt-catalyzed hydrosilylation/Pd-catalyzed cross-coupling reactions. Organic Letters. 3: 1073-6. PMID 11277798 DOI: 10.1021/Ol0156751 |
0.501 |
|
| 2001 |
Denmark SE, Guagnano V, Vaugeois J. Studies on the reduction and hydrolysis of nitroso acetals Canadian Journal of Chemistry. 79: 1606-1616. DOI: 10.1139/V01-132 |
0.368 |
|
| 2001 |
Denmark SE, Fujimori S. Diastereoselective aldol addition reactions of a chiral methyl ketone trichlorosilyl enolate under lewis base catalysis Synlett. 1024-1029. DOI: 10.1055/S-2001-14652 |
0.691 |
|
| 2001 |
Denmark SE, Wang Z. 1-Methyl-1-vinyl- and 1-Methyl-1-(prop-2-enyl)silacyclobutane: Reagents for palladium-catalyzed cross-coupling reactions of aryl halides Synthesis. 999-1003. DOI: 10.1055/S-2000-6292 |
0.461 |
|
| 2001 |
Denmark SE, Wang Z. Cross-coupling of vinylpolysiloxanes with aryl iodides Journal of Organometallic Chemistry. 624: 372-375. DOI: 10.1016/S0022-328X(00)00894-9 |
0.456 |
|
| 2001 |
Denmark SE, Stavenger RA. ChemInform Abstract: The Chemistry of Trichlorosilyl Enolates. Aldol Addition Reactions of Methyl Ketones. Cheminform. 32: no-no. DOI: 10.1002/chin.200101043 |
0.729 |
|
| 2000 |
Denmark SE, Neuville L. Mild and general cross-coupling of (alpha-Alkoxyvinyl)silanols and -silyl hydrides Organic Letters. 2: 3221-4. PMID 11009386 DOI: 10.1021/Ol0064112 |
0.434 |
|
| 2000 |
Denmark SE, Wehrli D, Choi JY. Convergence of mechanistic pathways in the Palladium(0)-catalyzed cross-coupling of alkenylsilacyclobutanes and alkenylsilanols Organic Letters. 2: 2491-4. PMID 10956529 DOI: 10.1021/Ol006170Y |
0.459 |
|
| 2000 |
Denmark SE, Stavenger RA. Asymmetric catalysis of aldol reactions with chiral lewis bases. Accounts of Chemical Research. 33: 432-40. PMID 10891061 DOI: 10.1021/Ar960027G |
0.781 |
|
| 2000 |
Denmark SE, Jacobsen EN. Catalytic asymmetric synthesis. Accounts of Chemical Research. 33: 324. PMID 10891049 DOI: 10.1021/Ar000046X |
0.473 |
|
| 2000 |
Denmark SE, Wehrli D. Highly stereospecific, palladium-catalyzed cross-coupling of alkenylsilanols Organic Letters. 2: 565-8. PMID 10814378 DOI: 10.1021/Ol005565E |
0.511 |
|
| 2000 |
Denmark SE, Herbert B. Synthesis of (-)-7-epiaustraline and (-)-1-epicastanospermine. The Journal of Organic Chemistry. 65: 2887-96. PMID 10814174 DOI: 10.1021/Jo991990D |
0.38 |
|
| 2000 |
Denmark SE, Hurd AR. Synthesis of (+)-casuarine. The Journal of Organic Chemistry. 65: 2875-86. PMID 10814173 DOI: 10.1021/Jo991680V |
0.803 |
|
| 2000 |
Denmark SE, Kim JH. Diastereoselective alkylations of chiral, phosphorus-stabilized carbanions: N-alkyl substituent effects in P-alkyl-1,3,2-diazaphosphorinane 2-oxides Canadian Journal of Chemistry. 78: 673-688. DOI: 10.1139/V99-251 |
0.349 |
|
| 2000 |
Denmark SE, Fu J. On the mechanism of catalytic, enantioselective allylation of aldehydes with chlorosilanes and chiral Lewis bases [14] Journal of the American Chemical Society. 122: 12021-12022. DOI: 10.1021/Ja002060A |
0.623 |
|
| 2000 |
Denmark SE, Stavenger RA. The chemistry of trichlorosilyl enolates. Aldol addition reactions of methyl ketones Journal of the American Chemical Society. 122: 8837-8847. DOI: 10.1021/Ja001023G |
0.784 |
|
| 2000 |
Denmark SE, Wang Z. ChemInform Abstract: 1-Methyl-1-vinyl- and 1-Methyl-1-(prop-2-enyl)silacyclobutane: Reagents for Palladium-Catalyzed Cross-Coupling Reactions of Aryl Halides. Cheminform. 31: no-no. DOI: 10.1002/chin.200041047 |
0.356 |
|
| 2000 |
Denmark SE, Pham SM. Kinetic analysis of the divergence of reaction pathways in the chiral Lewis base promoted aldol additions of trichlorosilyl enol ethers: A Rapid-injection NMR study Helvetica Chimica Acta. 83: 1846-1853. DOI: 10.1002/1522-2675(20000809)83:8<1846::Aid-Hlca1846>3.0.Co;2-V |
0.682 |
|
| 1999 |
Denmark SE, Su X, Nishigaichi Y, Coe DM, Wong KT, Winter SB, Choi JY. Synthesis of Phosphoramides for the Lewis Base-Catalyzed Allylation and Aldol Addition Reactions. The Journal of Organic Chemistry. 64: 1958-1967. PMID 11674289 DOI: 10.1021/Jo9820723 |
0.457 |
|
| 1999 |
Denmark SE, Seierstad M. Tandem Cycloaddition Chemistry of Nitroalkenes: Probing the Remarkable Stereochemical Influence of the Lewis Acid. The Journal of Organic Chemistry. 64: 1610-1619. PMID 11674226 DOI: 10.1021/Jo9820869 |
0.741 |
|
| 1999 |
Denmark SE, Seierstad M, Herbert B. Tandem Cycloaddition Chemistry of Nitroalkenes: Preparative and Theoretical Studies on the Stereochemical Course of [3 + 2] Cycloaddition of Cyclic Nitronates. The Journal of Organic Chemistry. 64: 884-901. PMID 11674161 DOI: 10.1021/Jo9818374 |
0.753 |
|
| 1999 |
Denmark SE, Hurd AR. Synthesis of (+)-casuarine. Organic Letters. 1: 1311-4. PMID 10825980 DOI: 10.1021/Ol9909886 |
0.798 |
|
| 1999 |
Denmark SE, Wu Z. The Development of Chiral, Nonracemic Dioxiranes for the Catalytic, Enantioselective Epoxidation of Alkenes Synlett. 1999: 847-859. DOI: 10.1055/S-1999-3123 |
0.771 |
|
| 1999 |
Denmark SE, Wu Z. Synthesis of Unsymmetrical Biaryls from Arylsilacyclobutanes Organic Letters. 1: 1495-1498. DOI: 10.1021/Ol991054K |
0.799 |
|
| 1999 |
Denmark SE, Choi JY. Highly stereospecific, cross-coupling reactions of alkenylsilacyclobutanes Journal of the American Chemical Society. 121: 5821-5822. DOI: 10.1021/Ja9908117 |
0.44 |
|
| 1999 |
Denmark SE, Stavenger RA, Wong KT, Su X. Chiral phosphoramide-catalyzed aldol additions of ketone enolates. Preparative aspects Journal of the American Chemical Society. 121: 4982-4991. DOI: 10.1021/Ja984123J |
0.781 |
|
| 1999 |
Denmark SE, Martinborough EA. Enantioselective Total Syntheses of (+)-Castanospermine, (+)-6-Epicastanospermine, (+)-Australine, and (+)-3-Epiaustraline Journal of the American Chemical Society. 121: 3046-3056. DOI: 10.1021/Ja9829970 |
0.473 |
|
| 1999 |
Denmark SE, Su X. Solid state and solution structural studies of chiral phosphoramide-tin complexes relevant to Lewis base catalyzed aldol reactions Tetrahedron. 55: 8727-8738. DOI: 10.1016/S0040-4020(99)00439-1 |
0.365 |
|
| 1998 |
Denmark SE, O'Connor SP, Wilson SR. Solution and Solid-State Studies of a Chiral Zinc-Sulfonamide Complex Relevant to Enantioselective Cyclopropanations. Angewandte Chemie (International Ed. in English). 37: 1149-1151. PMID 29711011 DOI: 10.1002/(Sici)1521-3773(19980504)37:8<1149::Aid-Anie1149>3.0.Co;2-F |
0.32 |
|
| 1998 |
Denmark SE, Dixon JA. Tandem Inter [4 + 2]/Intra [3 + 2] Cycloadditions of Nitroalkenes. Asymmetric Synthesis of Highly Functionalized Aminocyclopentanes Using the Bridged Mode (beta-Tether) Process. The Journal of Organic Chemistry. 63: 6178-6195. PMID 11672248 DOI: 10.1021/Jo9802170 |
0.433 |
|
| 1998 |
Denmark SE, Dixon JA. Tandem Inter [4 + 2]/Intra [3 + 2] Cycloadditions of Nitroalkenes. The Bridged Mode (beta-Tether). The Journal of Organic Chemistry. 63: 6167-6177. PMID 11672247 DOI: 10.1021/Jo9802168 |
0.422 |
|
| 1998 |
Denmark SE, Barsanti PA, Wong KT, Stavenger RA. Enantioselective Ring Opening of Epoxides with Silicon Tetrachloride in the Presence of a Chiral Lewis Base. The Journal of Organic Chemistry. 63: 2428-2429. PMID 11672098 DOI: 10.1021/Jo9801420 |
0.821 |
|
| 1998 |
Denmark SE, Stavenger RA, Su X, Wong K, Nishigaichi Y. Asymmetric catalysis with chiral Lewis bases Pure and Applied Chemistry. 70: 1469-1476. DOI: 10.1351/Pac199870081469 |
0.779 |
|
| 1998 |
Denmark SE, Stavenger RA, Winter SBD, Wong KT, Barsanti PA. Preparation of chlorosilyl enolates Journal of Organic Chemistry. 63: 9517-9523. DOI: 10.1021/Jo981740H |
0.824 |
|
| 1998 |
Denmark SE, Stavenger RA. Highly 1,4-syn diastereoselective, phosphoramide-catalyzed aldol additions of chiral methyl ketone enolates Journal of Organic Chemistry. 63: 9524-9527. DOI: 10.1021/Jo981739I |
0.752 |
|
| 1998 |
Denmark SE, Wu Z. 6-Oxo-1,1,4,4-tetramethyl-1,4-diazepinium Salts. A New Class of Catalysts for Efficient Epoxidation of Olefins with Oxone† The Journal of Organic Chemistry. 63: 2810-2811. DOI: 10.1021/Jo980342B |
0.734 |
|
| 1998 |
Denmark SE, Hurd AR. Tandem [4 + 2]/[3 + 2] Cycloadditions with Nitroethylene The Journal of Organic Chemistry. 63: 3045-3050. DOI: 10.1021/Jo972280F |
0.807 |
|
| 1998 |
Denmark SE, Stavenger RA, Wong K. Lewis Base-Catalyzed, Asymmetric Aldol Additions of Methyl Ketone Enolates† The Journal of Organic Chemistry. 63: 918-919. DOI: 10.1021/Jo972168H |
0.738 |
|
| 1998 |
Denmark SE, Middleton DS. Tandem Inter [4 + 2]/Intra [3 + 2] Cycloadditions. 17. The Spiro Mode. Efficient and Highly Selective Synthesis of Azapropellanes The Journal of Organic Chemistry. 63: 1604-1618. DOI: 10.1021/Jo9719057 |
0.463 |
|
| 1998 |
Denmark SE, Su X, Nishigaichi Y. The Chemistry of Trichlorosilyl Enolates. 6. Mechanistic Duality in the Lewis Base-Catalyzed Aldol Addition Reaction Journal of the American Chemical Society. 120: 12990-12991. DOI: 10.1021/Ja982993V |
0.483 |
|
| 1998 |
Denmark SE, Stavenger RA, Wong KT. Asymmetric aldol additions catalyzed by chiral phosphoramides: Electronic effects of the aldehyde component Tetrahedron. 54: 10389-10402. DOI: 10.1016/S0040-4020(98)00493-1 |
0.769 |
|
| 1997 |
Denmark SE, Wu Z, Crudden CM, Matsuhashi H. Catalytic Epoxidation of Alkenes with Oxone. 2. Fluoro Ketones. The Journal of Organic Chemistry. 62: 8288-8289. PMID 11671961 DOI: 10.1021/Jo971781Y |
0.829 |
|
| 1997 |
Denmark SE, Dixon JA. Tandem Inter [4 + 2]/Intra [3 + 2] Cycloadditions of Nitroalkenes. A Versatile Asymmetric Synthesis of Highly Functionalized Aminocyclopentanes. The Journal of Organic Chemistry. 62: 7086-7087. PMID 11671805 DOI: 10.1021/Jo9713215 |
0.421 |
|
| 1997 |
Denmark SE, O'Connor SP. Enantioselective Cyclopropanation of Allylic Alcohols. The Effect of Zinc Iodide. The Journal of Organic Chemistry. 62: 3390-3401. PMID 11671728 DOI: 10.1021/Jo9702397 |
0.398 |
|
| 1997 |
Denmark SE, Stavenger RA, Faucher AM, Edwards JP. Cyclopropanation with Diazomethane and Bis(oxazoline)palladium(II) Complexes. The Journal of Organic Chemistry. 62: 3375-3389. PMID 11671727 DOI: 10.1021/Jo970044Z |
0.749 |
|
| 1997 |
Denmark SE, O'Connor SP. Catalytic, Enantioselective Cyclopropanation of Allylic Alcohols. Substrate Generality. The Journal of Organic Chemistry. 62: 584-594. PMID 11671453 DOI: 10.1021/Jo961859V |
0.348 |
|
| 1997 |
Denmark SE, Parker DL, Dixon JA. Tandem [4 + 2]/[3 + 2] Cycloadditions of Nitroalkenes. 12. Synthesis of (-)-Platynecine. The Journal of Organic Chemistry. 62: 435-436. PMID 11671424 DOI: 10.1021/Jo961919X |
0.431 |
|
| 1997 |
Denmark S, Winter S. The Chemistry of Chlorosilyl Enolates 3.: Variation of the Silyl Group and the Effect on Rate and Enantiomeric Excess of Acetate Aldol Additions Synlett. 1997: 1087-1089. DOI: 10.1055/S-1997-1543 |
0.334 |
|
| 1997 |
Denmark SE, Wu Z. Dioxiranes Are the Active Agents in Ketone-Catalyzed Epoxidations with Oxone The Journal of Organic Chemistry. 62: 8964-8965. DOI: 10.1021/Jo971500M |
0.725 |
|
| 1997 |
Denmark SE, Guagnano V, Dixon JA, Stolle A. Tandem Inter [4 + 2]/Intra [3 + 2] Cycloadditions of Nitroalkenes. 15. The Bridged Mode (α-Tether) The Journal of Organic Chemistry. 62: 4610-4628. DOI: 10.1021/Jo970686M |
0.411 |
|
| 1997 |
Denmark SE, Marcin LR. Asymmetric Construction of a Quaternary Carbon Center by Tandem [4 + 2]/[3 + 2] Cycloaddition of a Nitroalkene. The Total Synthesis of (−)-Mesembrine The Journal of Organic Chemistry. 62: 1675-1686. DOI: 10.1021/Jo970079Z |
0.472 |
|
| 1997 |
Denmark SE, Hurd AR, Sacha HJ. Tandem [4 + 2]/[3 + 2] cycloadditions of nitroalkenes. 13. The synthesis of (-)-detoxinine Journal of Organic Chemistry. 62: 1668-1674. DOI: 10.1021/Jo962306N |
0.797 |
|
| 1997 |
Denmark SE, Wong KT, Stavenger RA. The chemistry of trichlorosilyl enolates. 2. Highly-selective asymmetric aldol additions of ketone enolates Journal of the American Chemical Society. 119: 2333-2334. DOI: 10.1021/Ja9636698 |
0.74 |
|
| 1997 |
Denmark SE, Thorarensen A. Tandem [4 + 2]/[3 + 2] Cycloadditions of Nitroalkenes. 11. The Synthesis of (+)-Crotanecine Journal of the American Chemical Society. 119: 125-137. DOI: 10.1021/Ja963084D |
0.471 |
|
| 1996 |
Denmark SE, Thorarensen A. Tandem [4+2]/[3+2] Cycloadditions of Nitroalkenes. Chemical Reviews. 96: 137-166. PMID 11848747 DOI: 10.1021/Cr940277F |
0.443 |
|
| 1996 |
Denmark SE, Thorarensen A. Tandem [4 + 2]/[3 + 2] Cycloadditions of Nitroalkenes. 10. trans-2-(1-Methyl-1-phenylethyl)cyclohexanol as a New Auxiliary. The Journal of Organic Chemistry. 61: 6727-6729. PMID 11667549 DOI: 10.1021/Jo960912C |
0.385 |
|
| 1996 |
Dixon JA, Swiss KA, Denmark SE. rel-(1R,6S,7S,8R,9S)-9-methyl-8-phenyl-6-[(1s,2R)-(2-phenylcyclohexyl) oxy]-4-aza-3,5-dioxatricyclo[5.2.1.0(4,9)]decane. Acta Crystallographica. Section C, Crystal Structure Communications. 52: 2561-3. PMID 8900034 DOI: 10.1107/S0108270196006671 |
0.305 |
|
| 1996 |
Denmark SE, Christenson BL, O'Connor SP, Murase N. New vistas in organoelement chemistry Pure and Applied Chemistry. 68: 23-27. DOI: 10.1351/Pac199668010023 |
0.467 |
|
| 1996 |
Denmark S, Amburgey J. Stereoselective Synthesis of Trisubstituted Olefins Phosphorus, Sulfur, and Silicon and the Related Elements. 111: 196-196. DOI: 10.1080/10426509608054825 |
0.428 |
|
| 1996 |
Denmark SE, Nicaise OJ-. Ligand-mediated addition of organometallic reagents to azomethine functions Chemical Communications. 999-1004. DOI: 10.1039/Cc9960000999 |
0.399 |
|
| 1996 |
Denmark SE, Thorarensen A, Middleton DS. Tandem [4 + 2]/[3 + 2] Cycloadditions of Nitroalkenes. 9. Synthesis of (−)-Rosmarinecine Journal of the American Chemical Society. 118: 8266-8277. DOI: 10.1021/Ja961630X |
0.396 |
|
| 1996 |
Denmark SE, Winter SBD, Su X, Wong K. Chemistry of Trichlorosilyl Enolates. 1. New Reagents for Catalytic, Asymmetric Aldol Additions Journal of the American Chemical Society. 118: 7404-7405. DOI: 10.1021/Ja9606539 |
0.52 |
|
| 1996 |
Denmark SE, Senanayake C. Tandem inter [4+2]/intra [3+2] cycloadditions. 8. Cycloadditions with unactivated dipolarophiles Tetrahedron. 52: 11579-11600. DOI: 10.1016/0040-4020(96)00642-4 |
0.49 |
|
| 1995 |
Denmark SE, Kim J. Asymmetric Michael Addition Reaction of Phosphorus-Stabilized Allyl Anions with Cyclic Enones The Journal of Organic Chemistry. 60: 7535-7547. DOI: 10.1021/Jo00128A028 |
0.464 |
|
| 1995 |
Denmark SE, Nakajima N, Nicaise OJ, Faucher A, Edwards JP. Preparation of Chiral Bisoxazolines: Observations on the Effect of Substituents The Journal of Organic Chemistry. 60: 4884-4892. DOI: 10.1021/Jo00120A036 |
0.364 |
|
| 1995 |
Denmark SE, Thorarensen A, Middleton DS. A General Strategy for the Synthesis of Cis-Substituted Pyrrolizidine Bases. The Synthesis of (-)-Rosmarinecine The Journal of Organic Chemistry. 60: 3574-3575. DOI: 10.1021/Jo00117A002 |
0.39 |
|
| 1995 |
Denmark SE, Marcin LR. Asymmetric Nitroalkene [4 + 2] Cycloadditions: Enantioselective Synthesis of 3-Substituted and 3,4-Disubstituted Pyrrolidines The Journal of Organic Chemistry. 60: 3221-3235. DOI: 10.1021/Jo00115A043 |
0.507 |
|
| 1995 |
Denmark SE, Schnute ME, Marcin LR, Thorarensen A. Nitroalkene Inter [4 + 2]/Intra [3 + 2] Tandem Cycloadditions. 7. Application of (R)-(-)-2,2-Diphenylcyclopentanol as the Chiral Auxiliary The Journal of Organic Chemistry. 60: 3205-3220. DOI: 10.1021/Jo00115A042 |
0.319 |
|
| 1995 |
Denmark SE, Forbes DC, Hays DS, DePue JS, Wilde RG. Catalytic Epoxidation of Alkenes with Oxone The Journal of Organic Chemistry. 60: 1391-1407. DOI: 10.1021/Jo00110A049 |
0.457 |
|
| 1995 |
Denmark SE, Schnute ME. Palladium-Promoted Intramolecular Addition of an Aryl Iodide to a Nitroalkene The Journal of Organic Chemistry. 60: 1013-1019. DOI: 10.1021/Jo00109A037 |
0.472 |
|
| 1995 |
Denmark SE, Chen C. Alkylations of Chiral, Phosphoryl- and Thiophosphoryl-Stabilized Carbanions Journal of the American Chemical Society. 117: 11879-11897. DOI: 10.1021/Ja00153A009 |
0.323 |
|
| 1995 |
Denmark SE, Miller PC. Asymmetric [2,3]-Wittig rearrangements with chiral, phosphorus anion-stabilizing groups Tetrahedron Letters. 36: 6631-6634. DOI: 10.1016/00404-0399(50)1391-T |
0.428 |
|
| 1995 |
Denmark SE, Christenson BL, O'Connor SP. Catalytic enantioselective cyclopropanation with bis(halomethyl)zinc reagents. II. The effect of promoter structure on selectivity Tetrahedron Letters. 36: 2219-2222. DOI: 10.1016/0040-4039(95)00259-F |
0.415 |
|
| 1995 |
Denmark SE, Christenson BL, Coe DM, O'Connor SP. Catalytic enantioselective cyclopropanation with bis(halomethyl)zinc reagents. I. Optimization of reaction protocol Tetrahedron Letters. 36: 2215-2218. DOI: 10.1016/0040-4039(95)00258-E |
0.444 |
|
| 1995 |
Denmark SE, Chen C. Enantioselective synthesis of alkylidene cyclohexanes by an asymmetric olefination/cross-coupling sequence Heteroatom Chemistry. 6: 133-144. DOI: 10.1002/Hc.520060207 |
0.483 |
|
| 1995 |
DENMARK SE, NAKAJIMA N, NICAISE OJ. ChemInform Abstract: Asymmetric Addition of Organolithium Reagents to Imines. Cheminform. 26: no-no. DOI: 10.1002/chin.199516113 |
0.38 |
|
| 1995 |
DENMARK SE, COE DM, PRATT NE, GRIEDEL BD. ChemInform Abstract: Asymmetric Allylation of Aldehydes with Chiral Lewis Bases. Cheminform. 26: no-no. DOI: 10.1002/chin.199516030 |
0.386 |
|
| 1994 |
Denmark SE, Schnute ME, Thorarensen A, Middleton DS, Stolle A. The tandem cycloaddition chemistry of nitroalkenes Pure and Applied Chemistry. 66: 2041-2044. DOI: 10.1351/Pac199466102041 |
0.431 |
|
| 1994 |
Denmark SE, Rivera I. Asymmetric Carboalkoxyalkylidenation with a Chiral Horner-Wadsworth-Emmons Reagent The Journal of Organic Chemistry. 59: 6887-6889. DOI: 10.1021/Jo00102A005 |
0.433 |
|
| 1994 |
Denmark SE, Coe DM, Pratt NE, Griedel BD. Asymmetric Allylation of Aldehydes with Chiral Lewis Bases The Journal of Organic Chemistry. 59: 6161-6163. DOI: 10.1021/Jo00100A013 |
0.475 |
|
| 1994 |
Denmark SE, Thorarensen A. The Tandem Cycloaddition Chemistry of Nitroalkenes. A Novel Synthesis of (-)-Hastanecine The Journal of Organic Chemistry. 59: 5672-5680. DOI: 10.1021/Jo00098A027 |
0.524 |
|
| 1994 |
Denmark SE, Griedel BD. Chemistry of Enoxysilacyclobutanes. 3. Uncatalyzed, Syn-Selective, Asymmetric Aldol Additions The Journal of Organic Chemistry. 59: 5136-5138. DOI: 10.1021/Jo00097A010 |
0.435 |
|
| 1994 |
Denmark SE, Almstead NG. Stereochemical studies on the addition of allylstannanes to aldehydes. The SE' component Journal of Organic Chemistry. 59: 5130-5132. DOI: 10.1021/Jo00097A009 |
0.302 |
|
| 1994 |
Denmark SE, Schnute ME. Nitroalkene [4 + 2] Cycloadditions with 2-(Acyloxy)vinyl Ethers. Stereoselective Synthesis of 3-Hydroxy-4-substituted-pyrrolidines The Journal of Organic Chemistry. 59: 4576-4595. DOI: 10.1021/Jo00095A038 |
0.47 |
|
| 1994 |
Denmark SE, Chen C. Alkylation of Chiral, Phosphorus-Stabilized Carbanions: Substituent Effects on the Alkylation Selectivity The Journal of Organic Chemistry. 59: 2922-2924. DOI: 10.1021/Jo00090A004 |
0.407 |
|
| 1994 |
Denmark SE, Lee W. Investigations on Transition-State Geometry in the Lewis Acid- (Mukaiyama) and Fluoride-Promoted Aldol Reactions The Journal of Organic Chemistry. 59: 707-709. DOI: 10.1021/Jo00083A005 |
0.39 |
|
| 1994 |
Denmark SE, Nakajima N, Nicaise OJ. Asymmetric Addition of Organolithium Reagents to Imines Journal of the American Chemical Society. 116: 8797-8798. DOI: 10.1021/Ja00098A044 |
0.51 |
|
| 1994 |
Denmark SE, Griedel BD, Coe DM, Schnute ME. Chemistry of Enoxysilacyclobutanes: Highly Selective Uncatalyzed Aldol Additions Journal of the American Chemical Society. 116: 7026-7043. DOI: 10.1021/Ja00095A004 |
0.489 |
|
| 1994 |
Cramer CJ, Denmark SE, Miller PC, Dorow RL, Swiss KA, Wilson SR. Structure and Dynamics of Phosphorus(V)-Stabilized Carbanions: A Comparison of Theoretical, Crystallographic, and Solution Structures Journal of the American Chemical Society. 116: 2437-2447. DOI: 10.1021/Ja00085A026 |
0.403 |
|
| 1994 |
Denmark SE, Chen C. Triarylcarbenium ions as catalysts in the Mukaiyama Aldol addition: A mechanistic investigation Tetrahedron Letters. 35: 4327-4330. DOI: 10.1016/S0040-4039(00)73345-4 |
0.47 |
|
| 1993 |
Denmark SE, Nicaise O. Organocerium Additions to Chiral α,α-Dialkoxy Hydrazones: Asymmetric Synthesis ofN-Protected α-Amino Acetals and α-Amino Aldehydes Synlett. 1993: 359-361. DOI: 10.1055/S-1993-22456 |
0.348 |
|
| 1993 |
Denmark SE, Marcin LR. Nitroalkene [4+2] cycloaddition as a general and stereoselective route to the synthesis of 3,3- and 3,4-disubstituted pyrrolidines The Journal of Organic Chemistry. 58: 3857-3868. DOI: 10.1021/Jo00067A017 |
0.419 |
|
| 1993 |
Denmark SE, Marcin LR. A general method for the preparation of 2,2-disubstituted 1-nitroalkenes The Journal of Organic Chemistry. 58: 3850-3856. DOI: 10.1021/Jo00067A016 |
0.395 |
|
| 1993 |
Denmark SE, Schnute ME, Senanayake CBW. Tandem inter [4+2]/intra [3+2]nitroalkene cycloadditions. 5. Origin of the Lewis acid dependent reversal of stereoselectivity The Journal of Organic Chemistry. 58: 1859-1874. DOI: 10.1021/Jo00059A044 |
0.44 |
|
| 1993 |
Denmark SE, Senanayake CBW. Tandem inter [4+2]/intra [3+2] nitroalkene cycloadditions. 4. Cycloadditions with (E)- and (Z)-1-propenyl ethers The Journal of Organic Chemistry. 58: 1853-1858. DOI: 10.1021/Jo00059A043 |
0.372 |
|
| 1993 |
Denmark SE, Griedel BD, Coe DM. The chemistry of enoxysilacyclobutanes: highly selective, uncatalyzed aldol additions The Journal of Organic Chemistry. 58: 988-990. DOI: 10.1021/Jo00057A002 |
0.369 |
|
| 1993 |
Denmark SE, Edwards JP, Nicaise O. Organocerium additions to hydrazones: effects of reagent stoichiometry on efficiency and selectivity The Journal of Organic Chemistry. 58: 569-578. DOI: 10.1021/Jo00055A008 |
0.347 |
|
| 1993 |
Denmark SE, Amburgey J. A new, general, and stereoselective method for the synthesis of trisubstituted alkenes Journal of the American Chemical Society. 115: 10386-10387. DOI: 10.1021/Ja00075A075 |
0.389 |
|
| 1993 |
Denmark SE, Almstead NG. Spectroscopic studies on the structure and conformation of Lewis acid-aldehyde complexes Journal of the American Chemical Society. 115: 3133-3139. DOI: 10.1021/Ja00061A012 |
0.33 |
|
| 1992 |
Denmark SE, Kim J. A Diastereoselective Synthesis of (dl)-1,3-Diphenyl-1,3-propanediamines Synthesis. 1992: 229-234. DOI: 10.1055/S-1992-34183 |
0.351 |
|
| 1992 |
Denmark SE, Kesler BS, Moon YC. Inter- and intramolecular [4 + 2] cycloadditions of nitroalkenes with olefins. 2-Nitrostyrenes The Journal of Organic Chemistry. 57: 4912-4924. DOI: 10.1021/Jo00044A029 |
0.453 |
|
| 1992 |
Denmark SE, Chen CT. Electrophilic activation of the Horner-Wadsworth-Emmons-Wittig reaction: highly selective synthesis of dissymmetric olefins Journal of the American Chemical Society. 114: 10674-10676. DOI: 10.1021/Ja00052A094 |
0.475 |
|
| 1992 |
Denmark SE, Forbes DC. A stereochemical study on the intramolecular hydrosilylation of α,β-unsaturated esters Tetrahedron Letters. 33: 5037-5040. DOI: 10.1016/S0040-4039(00)61182-6 |
0.323 |
|
| 1992 |
Denmark SE, Chatani N, Pansare SV. Asymmetric electrophilic amination of chiral phosphorus-stabilized anions Tetrahedron. 48: 2191-2208. DOI: 10.1016/S0040-4020(01)88883-9 |
0.704 |
|
| 1992 |
Denmark SE, Lee W. Investigations on transition state geometry of the aldol condensation in aqueous medium Tetrahedron Letters. 33: 7729-7732. DOI: 10.1016/0040-4039(93)88030-M |
0.314 |
|
| 1992 |
Denmark SE, Almstead NG. Spectroscopic studies on the TiCl4-promoted reaction of allylsilanes with aldehydes and α,β-enones Tetrahedron. 48: 5565-5578. DOI: 10.1016/0040-4020(92)80007-3 |
0.388 |
|
| 1991 |
Willson TM, Amburgey J, Denmark SE. Synthesis of α- and β-branched ethers from alcohols by reaction of acetals with grignard reagents: synthesis of isopropyl and isobutyl ethers of (1S*,2R*S*,4R*)-6-methylenebicyclo[2.2.2]octan-2-ol Journal of the Chemical Society-Perkin Transactions 1. 2899-2906. DOI: 10.1039/P19910002899 |
0.451 |
|
| 1991 |
Denmark SE, Edwards JP. A comparison of (chloromethyl)- and (iodomethyl)zinc cyclopropanation reagents The Journal of Organic Chemistry. 56: 6974-6981. DOI: 10.1021/Jo00025A007 |
0.315 |
|
| 1991 |
Denmark SE, Almstead NG. Stereoselective opening of chiral dioxane acetals. Nucleophile dependence The Journal of Organic Chemistry. 56: 6485-6487. DOI: 10.1021/Jo00023A002 |
0.445 |
|
| 1991 |
Denmark SE, Almstead NG. On the stereoselectivity opening of achiral dioxane acetals The Journal of Organic Chemistry. 56: 6458-6467. DOI: 10.1021/Jo00022A043 |
0.408 |
|
| 1991 |
Denmark SE, Marlin JE. Carbanion-accelerated Claisen rearrangements. 7. Phosphine oxide and phosphonate anion stabilizing groups The Journal of Organic Chemistry. 56: 1003-1013. DOI: 10.1021/Jo00003A021 |
0.365 |
|
| 1991 |
Denmark SE, Almstead NG. Studies on the mechanism and origin of stereoselective opening of chiral dioxane acetals Journal of the American Chemical Society. 113: 8089-8110. DOI: 10.1021/Ja00021A040 |
0.398 |
|
| 1991 |
Denmark SE, Henke BR. Investigations on transition-state geometry in the aldol condensation. Journal of the American Chemical Society. 113: 2177-2194. DOI: 10.1021/Ja00006A042 |
0.361 |
|
| 1990 |
Denmark SE, Jacobs RT, Dai-Ho G, Wilson S. Synthesis, structure, and reactivity of an organogermanium Lewis acid Organometallics. 9: 3015-3019. DOI: 10.1021/Om00162A006 |
0.391 |
|
| 1990 |
Denmark SE, Dorow RL. Stereoselective alkylations of chiral, phosphorus-stabilized benzylic carbanions The Journal of Organic Chemistry. 55: 5926-5928. DOI: 10.1021/Jo00311A003 |
0.457 |
|
| 1990 |
Denmark SE, Marble LK. Auxiliary-based, asymmetric SN2' reactions: a case of 1,7-relative stereogenesis The Journal of Organic Chemistry. 55: 1984-1986. DOI: 10.1021/Jo00294A006 |
0.404 |
|
| 1990 |
Denmark SE, Cramer CJ. The theoretical structures of neutral, anionic, and lithiated P-allylphosphonic diamide The Journal of Organic Chemistry. 55: 1806-1813. DOI: 10.1021/Jo00293A026 |
0.408 |
|
| 1990 |
Denmark SE, Dappen MS, Sear NL, Jacobs RT. The vinylogous anomeric effect in 3-alkyl-2-chlorocyclohexanone oximes and oxime ethers Journal of the American Chemical Society. 112: 3466-3474. DOI: 10.1021/Ja00165A034 |
0.377 |
|
| 1990 |
Denmark SE, Moon YC, Senanayake CBW. Tandem [4 + 2]/[3 + 2] cycloadditions: facile and stereoselective construction of polycyclic frameworks Journal of the American Chemical Society. 112: 311-315. DOI: 10.1021/Ja00157A048 |
0.401 |
|
| 1990 |
Denmark SE, Moon Y, Cramer CJ, Dappen MS, Senanayake C. Intramolecular [4+2]-cycloadditions of nitroalkenes with olefins. 2 Tetrahedron. 46: 7373-7392. DOI: 10.1016/S0040-4020(01)89054-2 |
0.573 |
|
| 1990 |
Denmark SE, Senanayake C, Ginny-Dai H. Tandem [4+2]/[3+2]-cycloadditions. 2. Asymmetric induction with a chiral vinyl ether Tetrahedron. 46: 4857-4876. DOI: 10.1016/S0040-4020(01)85599-X |
0.428 |
|
| 1990 |
DENMARK SE, SENANAYAKE CBW, HO G. ChemInform Abstract: Tandem (4 + 2)/(3 + 2)-Cycloadditions. Part 2. Asymmetric Induction with a Chiral Vinyl Ether. Cheminform. 21. DOI: 10.1002/chin.199044069 |
0.362 |
|
| 1990 |
DENMARK SE, MARBLE LK. ChemInform Abstract: Auxiliary-Based, Asymmetric SN2′ Reactions: A Case of 1,7-Relative Stereogenesis. Cheminform. 21. DOI: 10.1002/chin.199036054 |
0.303 |
|
| 1990 |
DENMARK SE, DAPPEN MS, SEAR NL, JACOBS RT. ChemInform Abstract: The Vinylogous Anomeric Effect in 3-Alkyl-2-chlorocyclohexanone Oximes and Oxime Ethers. Cheminform. 21. DOI: 10.1002/chin.199034101 |
0.307 |
|
| 1990 |
DENMARK SE, HARMATA MA, WHITE KS. ChemInform Abstract: Carbanion-Accelerated Claisen Rearrangements. Part 6. Preparative and Stereochemical Studies with Sulfonyl-Stabilized Anions. Cheminform. 21. DOI: 10.1002/chin.199012061 |
0.507 |
|
| 1989 |
Weber T, Edwards J, Denmark S. Modified Proline Auxiliaries for Selective Addition of Organocerium Reagents to Hydrazones Synlett. 1989: 20-22. DOI: 10.1055/S-1989-34682 |
0.307 |
|
| 1989 |
Denmark SE, Dorow RL. The stereochemical course of migration from phosphorus to nitrogen in the photo-Curtius rearrangement of phosphinic azides (Harger reaction) The Journal of Organic Chemistry. 54: 5-6. DOI: 10.1021/Jo00262A002 |
0.423 |
|
| 1989 |
Denmark SE, Harmata MA, White KS. Carbanion-accelerated Claisen rearrangements. 6. Preparative and stereochemical studies with sulfonyl-stabilized anions Journal of the American Chemical Society. 111: 8878-8891. DOI: 10.1021/Ja00206A017 |
0.546 |
|
| 1989 |
Denmark SE, Willson TM. Mechanistic and stereochemical divergence in the allylsilane-acetal addition reaction Journal of the American Chemical Society. 111: 3475-3476. DOI: 10.1021/Ja00191A079 |
0.439 |
|
| 1989 |
Denmark SE, Rajendra G, Marlin JE. Carbanion-accelerated Claisen rearrangements 5. Studies on stereocontrol with phosphorus-stabilized anions Tetrahedron Letters. 30: 2469-2472. DOI: 10.1016/S0040-4039(01)80427-5 |
0.412 |
|
| 1989 |
Denmark SE, Weber EJ, Wilson TM, Willson TM. Stereochemical and spectroscopic studies on the reaction of allylstannanes with aldehydes Tetrahedron. 45: 1053-1065. DOI: 10.1016/0040-4020(89)80016-X |
0.437 |
|
| 1989 |
DENMARK SE, WILLSON TM. ChemInform Abstract: Mechanistic and Stereochemical Divergence in the Allylsilane-Acetal Addition Reaction. Cheminform. 20. DOI: 10.1002/chin.198933070 |
0.356 |
|
| 1989 |
DENMARK SE, DOROW RL. ChemInform Abstract: The Stereochemical Course of Migration from Phosphorus to Nitrogen in the Photo-Curtius Rearrangement of Phosphinic Azides (Harger Reaction). Cheminform. 20. DOI: 10.1002/chin.198928124 |
0.331 |
|
| 1989 |
DENMARK SE, WEBER EJ, WILSON TM, WILLSON TM. ChemInform Abstract: Stereochemical and Spectroscopic Studies on the Reaction of Allylstannanes with Aldehydes. Cheminform. 20. DOI: 10.1002/chin.198927114 |
0.352 |
|
| 1988 |
Denmark SE, Ares JJ. Stereoselective alkylation of chiral .alpha.-nitro keto imine dianions. Observations on the role of amide bases Journal of the American Chemical Society. 110: 4432-4434. DOI: 10.1021/Ja00221A064 |
0.365 |
|
| 1988 |
Denmark SE, Wilson T, Willson TM. On the Lewis-acid-induced addition of allylstannanes to aldehydes: a spectroscopic investigation Journal of the American Chemical Society. 110: 984-986. DOI: 10.1021/Ja00211A058 |
0.303 |
|
| 1988 |
Denmark SE, Hite GA. Silicon-DirectedNazarov Cyclizations. Part VI. The anomalous cyclization of vinyl dienyl ketones Helvetica Chimica Acta. 71: 195-208. DOI: 10.1002/Hlca.19880710121 |
0.468 |
|
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