Stereospecific thio-claisen rearrangement of S-crotylic α-hydroxy ketene dithioacetals. Creation of three contiguous stereogenic centres.
- 1 April 1993
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 49 (15) , 3131-3142
- https://doi.org/10.1016/s0040-4020(01)89896-3
Abstract
No abstract availableKeywords
This publication has 60 references indexed in Scilit:
- Prelog-Djerassi Lactonic Acid. A Target for Design and Development of Stereoselective Synthetic MethodsSynthesis, 1991
- Aza-claisen rearrangement of amide enolates. Stereoselective synthesis of 2,3-disubstituted carboxamidesTetrahedron Letters, 1990
- The Hetero-Cope Rearrangement in Organic SynthesisSynthesis, 1989
- The thermal, aliphatic Claisen rearrangementChemical Reviews, 1988
- Catalysis of the Cope and Claisen rearrangementsChemical Reviews, 1984
- Diastereoselective synthesis of erythro- and threo-2-hydroxy-3-methyl-4-pentenoic acids by the ester enolate claisen rearrangement of 2-butenyl 2-hydroxyacetateTetrahedron Letters, 1983
- Stereocontrol in the synthesis of acyclic systems: applications to natural product synthesisTetrahedron, 1980
- Stereo- and regiochemistry of the Claisen rearrangement: applications to natural products synthesisAccounts of Chemical Research, 1977
- The Claisen Rearrangement in Organic Synthesis; 1967 to January 1977Synthesis, 1977
- The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formationJournal of the American Chemical Society, 1976