Highly Regio- and Stereoselective [3+2] Cyclopentanone Annulation Using a 3-(Alkylthio)-2-siloxyallyl Cationic Species
- 14 February 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 120 (8), 1724-1731
- https://doi.org/10.1021/ja972879x
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Diastereoselective Introduction of Carbon Chain to Pyrrolidone DerivativesSynlett, 1996
- Bis(sulfonyl) Ketones: A New Oxyallyl Cation SourceThe Journal of Organic Chemistry, 1995
- Conjugate Addition of Alkenylsulfides with α,β-Unsaturated Carbonyl Compounds. Remarkable n-π* Orbital Interaction for Control of Regio- and StereochemistrySynlett, 1995
- 3-(alkylthio)-1,2-bis(siloxy)-3-butenes as efficient chirality transferred building blocksTetrahedron Letters, 1994
- Highly Stereoselective Ene Reaction of Aldimines with 2-(Alkylthio)allyl Silyl EthersThe Journal of Organic Chemistry, 1994
- A novel transformation involving selective formation and cleavage of carbon-carbon bondsJournal of the American Chemical Society, 1993
- An enantioselective synthesis of anthracycline precursorsThe Journal of Organic Chemistry, 1993
- Selenium-directed stereoselective [2 + 2] cycloaddition reactions promoted by Lewis acids: a novel zwitterionic intermediateThe Journal of Organic Chemistry, 1992
- Remarkable Stereochemical Features of Ene Reaction of 2-(Alkylthio)crotyl Silyl Ethers Proposal of a Six-Membered Chair-like Transition StateChemistry Letters, 1992
- Optimization of parameters for semiempirical methods I. MethodJournal of Computational Chemistry, 1989