Stereochemical analysis of totally stereoselective competing [1,2]- and 2,3]-Wittig rearrangements. Inversion at the lithium-bearing carbon atom
- 1 January 1992
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 114 (1) , 375-377
- https://doi.org/10.1021/ja00027a066
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- An expedient and high yielding synthesis of mefloquine. Via fluoride ion-catalyzed Wittig rearrangement ITetrahedron, 1989
- Enantioselective synthesis of macrocyclic propargylic alcohols by [2,3] Wittig ring contraction. Synthesis of (+)-aristolactone and cembranoid precursorsJournal of the American Chemical Society, 1988
- Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatizationJournal of the American Chemical Society, 1987