Studies on the total synthesis of lactacystin. An improved aldol coupling reaction and a β-lactone intermediate in thiol ester formation
- 29 October 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (44), 6977-6980
- https://doi.org/10.1016/s0040-4039(00)61575-7
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Total synthesis of lactacystinJournal of the American Chemical Society, 1992
- Anti‐Selective and Diastereofacially Selective Aldol Reactions with (R)‐2‐Siloxy‐1,2,2‐triphenylethyl propionateAngewandte Chemie International Edition in English, 1991
- Structure of lactacystin, a new microbial metabolite which induces differentiation of neuroblastoma cells.The Journal of Antibiotics, 1991
- Lactacystin, a novel microbial metabolite, induces neuritogenesis of neuroblastoma cells.The Journal of Antibiotics, 1991
- Acyclic stereoselection. 8. A new class of reagents for the highly stereoselective preparation of threo-2-alkyl-3-hydroxycarboxylic acids by the aldol condensationThe Journal of Organic Chemistry, 1980