Novel Asymmetric C−C Bond Formation Process Promoted by Et2AlCl and Its Application to the Stereoselective Synthesis of Unusual β-Branched Baylis−Hillman Adducts
- 13 January 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 64 (3), 1061-1064
- https://doi.org/10.1021/jo981976l
Abstract
No abstract availableThis publication has 37 references indexed in Scilit:
- Smaller Substituents on Nitrogen Facilitate the Osmium‐Catalyzed Asymmetric AminohydroxylationAngewandte Chemie International Edition in English, 1996
- Catalytic Asymmetric Aminohydroxylation Provides a Short Taxol Side-chain Synthesis.Acta Chemica Scandinavica, 1996
- Docetaxel (taxotere) derivatives: novel NbCl3-based stereoselective approach to 2′-methyldocetaxelJournal of the Chemical Society, Perkin Transactions 1, 1995
- Planar Chiral Arylaldehydeimine Tricarbonylchromium Complexes in the Asymmetric Baylis - Hillman Coupling ReactionSynlett, 1994
- Asymmetric synthesis of sulfinimines: applications to the synthesis of nonracemic .beta.-amino acids and .alpha.-hydroxyl .beta.-amino acidsThe Journal of Organic Chemistry, 1992
- Organocopper ReagentsPublished by Elsevier ,1991
- Conjugate reduction of .alpha.,.beta.-acetylenic ketones and esters by diisobutylaluminum hydride-hexamethylphosphoric triamideThe Journal of Organic Chemistry, 1987
- Chemistry of substituted [.alpha.-(carboethoxy)vinyl]cuprates and their synthetic application to cyclopentenone annulationsThe Journal of Organic Chemistry, 1981
- Synthetic studies on insect hormones. VIII. Stereospecific synthesis of trisubstituted olefins from organocopper reagents and acetylenesJournal of the American Chemical Society, 1969
- Stereospecific synthesis of trisubstituted and tetrasubstituted olefins. Conjugate addition of dialkylcopper-lithium reagents to .alpha.,.beta.-acetylenic estersJournal of the American Chemical Society, 1969