Enantioselective radical allylation of α-Iodoamides using chiral aluminum based Lewis acids
- 14 April 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (15) , 2661-2664
- https://doi.org/10.1016/s0040-4039(97)00411-5
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Chiral Lewis Acid Catalysis in Radical Reactions: Enantioselective Conjugate Radical AdditionsJournal of the American Chemical Society, 1996
- Enantioselective radical cyclization controlled by a chiral aluminium reagentChemical Communications, 1996
- Enantioselective Free Radical Carbon-Carbon Bond Forming Reactions: Chiral Lewis Acid Promoted Acyclic AdditionsJournal of the American Chemical Society, 1995
- Lewis Acid-Enhanced Reactivity of .alpha.,.beta.-Unsaturated Esters and Amides toward Radical AdditionThe Journal of Organic Chemistry, 1995
- Enantioselective radical-mediated reduction of α-iodolactone using tributyltin hydride in the presence of a chiral amine and a Lewis acidJournal of the Chemical Society, Chemical Communications, 1995
- Stereoselective Reactions of Sulfinylated Benzyl Radicals: Effects of Solvents and Lewis AcidsAngewandte Chemie International Edition in English, 1994
- Altering the Stereochemistry of Allylation Reactions of Cyclic .alpha.-Sulfinyl Radicals: Effects of Solvents and Lewis AcidsThe Journal of Organic Chemistry, 1994
- Catalytic asymmetric Diels Alder reactionsChemical Reviews, 1992
- Chiral Lewis Acids in Catalytic Asymmetric ReactionsSynthesis, 1991
- Asymmetric Diels-Alder cycloaddition reactions with chiral .alpha.,.beta.-unsaturated N-acyloxazolidinonesJournal of the American Chemical Society, 1988