Allylic Alcohols via Catalytic Asymmetric Epoxide Rearrangement
- 30 June 2000
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 122 (28) , 6610-6618
- https://doi.org/10.1021/ja000545t
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Stereoselective Diamine Chelates of a Chiral Lithium Amide Dimer: New Insights into the Coordination Chemistry of Chiral Lithium AmidesJournal of the American Chemical Society, 1999
- New and Highly Enantioselective Catalysts for the Rearrangement of meso-Epoxides into Chiral Allylic AlcoholsJournal of the American Chemical Society, 1998
- Iodohydrins: An Easy Route to Epoxides from AlkenesSynthetic Communications, 1998
- Design, Synthesis, and Application of Chiral Nonracemic Lithium Amide Bases in Enantioselective Deprotonation of EpoxidesThe Journal of Organic Chemistry, 1996
- Solution structures of lithium dialkylamides and related N-lithiated species: results from lithium-6-nitrogen-15 double labeling experimentsAccounts of Chemical Research, 1993
- Asymmetric induction in the ene reactions of N-sulfinylcarbamatesJournal of the American Chemical Society, 1990
- Application of the dibenzoate chirality method to determine the absolute configuration of glycerols and related acyclic alcoholsThe Journal of Organic Chemistry, 1990
- (R,R)-1,3-Dibenzylisoindoline: a new C2-symmetric secondary amine, by stereoselective and regioselective .alpha.,.alpha.'-dialkylation of isoindoline, and an improved procedure for the preparation of isoindolineThe Journal of Organic Chemistry, 1988
- Stereochemistry of the base-induced rearrangement of epoxides to allylic alcoholsJournal of the American Chemical Society, 1970
- The Stereochemistry of the 1-Phenyl-1,2-propanediols and of α-IsoephedrineJournal of the American Chemical Society, 1957