Highly stereoselective chelation controlled ene-reaction of 2-(alkylthio)allyl silyl ethers
- 1 January 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (3) , 477-480
- https://doi.org/10.1016/0040-4039(93)85106-7
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Remarkable Stereochemical Features of Ene Reaction of 2-(Alkylthio)crotyl Silyl Ethers Proposal of a Six-Membered Chair-like Transition StateChemistry Letters, 1992
- Ene reaction of 2-(alkylthio)allyl silyl ether involving a chirality transfer.Tetrahedron Letters, 1992
- Acyclic stereocontrol based on chelation-controlled ene reaction with chiral α- and β-alkoxyaldehydesTetrahedron: Asymmetry, 1990
- Carbonyl-ene reaction: An emerging tool for acyclic stereocontrol.Journal of Synthetic Organic Chemistry, Japan, 1990
- One-step stereochemical determination of four contiguous acyclic chiral centers on a steroidal side chain: a novel synthesis of brassinolideJournal of the American Chemical Society, 1986
- Chelation or Non‐Chelation Control in Addition Reactions of Chiral α‐ and β‐ Alkoxy Carbonyl Compounds [New Synthetic Methods (44)]Angewandte Chemie International Edition in English, 1984
- Stereoselective synthesis of plant growth-prompting steroids, brassinolide, castasterone, typhasterol, and their 28-nor analoguesJournal of the Chemical Society, Perkin Transactions 1, 1984
- Stereoselective synthesis of plant growth-promoting steroids, dolicholide and 28-norbrassinolideTetrahedron Letters, 1983
- Stereoselective synthesis of the plant-growth-promoting steroids dolicholide and dolichosteroneJournal of the Chemical Society, Perkin Transactions 1, 1983
- Lewis-acid catalyzed ene reactionsAccounts of Chemical Research, 1980