Enantioselective synthesis of curacin A. 1. Construction of C1–C7, C8–17, and C18–C22 segments
- 11 March 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (11) , 1795-1798
- https://doi.org/10.1016/0040-4039(96)00030-5
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Synthesis of Curacin A: A Powerful Antimitotic from the Cyanobacterium Lyngbya majusculaJournal of the American Chemical Society, 1995
- Diastereoface Discrimination in the Addition of Acetylide to a Chiral Aldehyde, Leading to a Synthesis of (+)-Deoxybiotin in Enantiomerically Pure Form Starting from L-CysteineThe Journal of Organic Chemistry, 1994
- Structure of Curacin A, a Novel Antimitotic, Antiproliferative and Brine Shrimp Toxic Natural Product from the Marine Cyanobacterium Lyngbya majusculaThe Journal of Organic Chemistry, 1994
- Synthesis of chiral vinylglycinesThe Journal of Organic Chemistry, 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
- A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compoundsThe Journal of Organic Chemistry, 1981
- The influence of chain-branching on the steric outcome of some olefin-forming reactionsJournal of the Chemical Society, Perkin Transactions 1, 1980
- An Improved Synthesis of Sulfones using Tetrabutyl-ammonium SulfinatesSynthesis, 1975
- A Stereoselective Synthesis of Methyl trans, trans-Farnesoate and Its Conversion to dl-C17-Cecropia Juvenile HormoneAgricultural and Biological Chemistry, 1974
- The Total Synthesis of Cephalosporin C1Journal of the American Chemical Society, 1966