Total Syntheses of Epothilones A and B via a Macrolactonization-Based Strategy
- 1 August 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (34), 7974-7991
- https://doi.org/10.1021/ja971110h
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Studies toward a Synthesis of Epothilone A: Stereocontrolled Assembly of the Acyl Region and Models for MacrocyclizationThe Journal of Organic Chemistry, 1996
- Studies toward a Synthesis of Epothilone A: Use of Hydropyran Templates for the Management of Acyclic Stereochemical RelationshipsThe Journal of Organic Chemistry, 1996
- Studies Towards the Total Synthesis of Epothilones: Asymmetric Synthesis of the Key FragmentsChemistry – A European Journal, 1996
- Enantioselective synthesis and determination of the configuration of stenusine, the spreading agent of the beetle Stenus commaThe Journal of Organic Chemistry, 1993
- High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoidsJournal of the American Chemical Society, 1991
- Chiral synthesis via organoboranes. 27. Remarkably rapid and exceptionally enantioselective (approaching 100% ee) allylboration of representative aldehydes at -100.degree. under new, salt-free conditionsThe Journal of Organic Chemistry, 1991
- Microbial transformations in organic synthesis. 4. Stereoselective fungal metabolism of 7-methylglaucineThe Journal of Organic Chemistry, 1986
- Stereoselective formation and electrophilic substitution of aldehyde hydrazone lithio anionsJournal of the American Chemical Society, 1979
- Molecular basis of thermostability in the lysozyme from bacteriophage T4Nature, 1979
- Sulfur trioxide in the oxidation of alcohols by dimethyl sulfoxideJournal of the American Chemical Society, 1967