TRANSFER OF ASYMMETRY BY THE PALLADIUM-CATALYZED ALKYLATION OF CHIRAL ALLYLIC SULFINATES
- 5 June 1984
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 13 (6) , 929-932
- https://doi.org/10.1246/cl.1984.929
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Neutral alkylations via palladium(0) catalysisJournal of the American Chemical Society, 1981
- New rules of selectivity: allylic alkylations catalyzed by palladiumAccounts of Chemical Research, 1980
- Allyl sulfones as synthons for 1,1- and 1,3-dipoles via organopalladium chemistryJournal of the American Chemical Society, 1980
- Allylic alkylation. Palladium-catalyzed substitutions of allylic carboxylates. Stereo- and regiochemistryJournal of the American Chemical Society, 1980
- Cyclization catalyzed by palladium(0). Initial studies and macrolide formationJournal of the American Chemical Society, 1980
- A stereocontrolled approach to acyclic systems. Stereorelay in charge-directed alkylations via organopalladium templatesJournal of the American Chemical Society, 1979
- Allylic substitutions with retention of stereochemistryThe Journal of Organic Chemistry, 1976
- Carbon-carbon bond formation via palladium complexesAccounts of Chemical Research, 1969
- Direct formylation of a methyl group in the oxo reaction. Formation of (R)-3-ethylhexanal in the hydroformylation of (S)(+)-3-methyl-1-hexeneJournal of the American Chemical Society, 1968
- The Stereochemistry of the Wolff RearrangementJournal of the American Chemical Society, 1956