1,3-dipolar cycloaddition reactions of azomethine ylides on enantiomerically pure (E)-γ-alkoxy-α,β-unsaturated esters.
- 31 December 1991
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 2 (12) , 1329-1342
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- The diastereoselectivity of intermolecular nitrone cycloaddition to chiral allyl derivativesTetrahedron Letters, 1991
- Directed nitrile oxide cycloaddition reactions. The use of hydrogen bonding to direct regio- and stereochemistry in nitrile oxide cycloadditions with cyclopentenylamidesThe Journal of Organic Chemistry, 1990
- Stereoselective intramolecular nitrone cycloadditions promoted by an allylic stereocenterThe Journal of Organic Chemistry, 1990
- An alternative enantioselective total synthesis of (+)-monomorine ITetrahedron Letters, 1990
- Recent Advances in Azomethine Ylide Chemistry1989
- Lithium bromide-triethylamine induced cycloaddition of N-alkylidene 2-amino esters and amides to electron-deficient olefins with high regio- and stereoselectivityThe Journal of Organic Chemistry, 1988
- Steric models for stereoselectivity of nitrile oxide cycloadditions to chiral alkenesJournal of the American Chemical Society, 1986
- Theory and Modeling of Stereoselective Organic ReactionsScience, 1986
- RECENT SYNTHETIC APPLICATIONS OF NITRONES. A REVIEWOrganic Preparations and Procedures International, 1985
- Stereoselective nitrile oxide cycloadditions to chiral allyl ethers and alcohols. The inside alkoxy effectJournal of the American Chemical Society, 1984