Stephen F. Martin
Affiliations: | University of Texas at Austin, Austin, Texas, U.S.A. |
Area:
Natural Product SynthesisWebsite:
http://www.cm.utexas.edu/stephen_martinGoogle:
"Stephen Martin"Bio:
http://chemistry.library.nd.edu/resources/genealogy/chemistry/documents/MartinSF.pdf
DOI: 10.1021/ar950230w
Mean distance: 7.57 | S | N | B | C | P |
Parents
Sign in to add mentorEdward Curtis Taylor | grad student | 1972 | Princeton | |
(I. New approaches toward the synthesis of 6- and 7-azapteridines. II. A new, general method for introducing alkyl substituents into heterocyclic nuclei.) | ||||
Rudolf Gompper | post-doc | 1973 | Universität München | |
George H. Büchi | post-doc | 1974 | MIT |
Children
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Publications
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Wang Z, Martin SF. (2020) Total Syntheses of (±)-Melicolones A and B. Organic Letters |
Lepovitz LT, Martin SF. (2020) Biomimetically Inspired, One-Step Synthesis of Exotine A and Exotine B. The Journal of Organic Chemistry |
Lepovitz LT, Meis AR, Thomas SM, et al. (2020) Design, Synthesis, and Evaluation of Novel Anti-Trypanosomal Compounds. Tetrahedron. 76 |
Wypych RM, LaPlante SR, White PW, et al. (2020) Structure-thermodynamics-relationships of hepatitis C viral NS3 protease inhibitors. European Journal of Medicinal Chemistry. 192: 112195 |
Blumberg S, Martin SF. (2020) Racemic or enantioselective osmium-catalyzed dihydroxylation of olefins under near-neutral conditions Arkivoc. 2021: 7-14 |
Goodnough AM, Sahn JJ, Martin SF. (2020) Facile entry to substituted 2-arylpiperidines via an aza-Sakurai reaction Tetrahedron Letters. 61: 151777 |
Wood MD, Klosowski DW, Martin SF. (2019) Stereoselective Total Synthesis of (±)-Alstoscholarisine E. Organic Letters |
Lepovitz LT, Martin SF. (2019) Diversity-Oriented Synthesis of Bioactive Azaspirocycles Tetrahedron. 75: 130637 |
Lepovitz LT, Martin SF. (2018) Biomimetically Inspired Synthesis of Exotine A. Organic Letters |
Klosowski DW, Hethcox JC, Paull DH, et al. (2018) Enantioselective Halolactonization Reactions using BINOL-derived Bifunctional Catalysts: Methodology, Diversification, and Applications. The Journal of Organic Chemistry |