Diastereoselection in the reactions of thioallylic anions with benzaldehyde
- 31 December 1980
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 21 (3) , 303-306
- https://doi.org/10.1016/s0040-4039(00)71196-8
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Stereoselective synthesis of β-hydroxy-α-methylketones via - and -vinyloxyboranes generated directly from cyclohexyl ethyl ketoneTetrahedron Letters, 1979
- Reactions of allylpyrrolidine carbanions with electrophiles. A new homoenolate equivalentTetrahedron Letters, 1977
- Acyclic stereoselection. 2. Synthesis of 3-hydroxy-2-methyl- and 3-hydroxy-2,4-dimethylcarboxylic acidsJournal of the American Chemical Society, 1977
- Reaction of gem-dichloroallyllithium with aldehydes, ketones, and other organic substrates. An example of electronic control of regioselectivity in the reactions of an ambident nucleophileJournal of the American Chemical Society, 1977
- Stereoselection in the aldol condensationJournal of the American Chemical Society, 1977
- Das Magnesium‐Derivat des Thioacrolein‐Dianions. Ein einfacher Zugang zu Vinyl‐ und DivinyloxiranenAngewandte Chemie, 1976
- Carbon-Carbon Bond Formation by Selective Coupling of Alkylthioallylcopper Reagent with Allylic HalidesBulletin of the Chemical Society of Japan, 1975
- Lithiated S-(2-methoxyallyl) N,N-dimethyldithiocarbamate, a new, versatile reagent for the introduction of the acetonyl functional group into organic substratesTetrahedron Letters, 1975
- C-alkylation of allyl, dithiocarbamates followed by allylicrearrangementTetrahedron Letters, 1974
- Metalated allylic ethers as homoenolate anion equivalentsJournal of the American Chemical Society, 1974