HETEROCONJUGATE ADDITION OF LITHIUM ALKYLS TO SUBSTITUTED HETERO-OLEFINS CONJUGATED WITH SULFUR AND SILICON ATOMS
- 5 March 1980
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 9 (3) , 331-334
- https://doi.org/10.1246/cl.1980.331
Abstract
Lithium alkyls and a lithiated sulfone carbanion readily added to the substituted hetero-olefins conjugated with silicon and sulfonesulfur atoms among other combination of the third (or fourth) row hetero atoms, e.g. Si, Se and S.This publication has 6 references indexed in Scilit:
- Vinyl phenyl selenide: a +CH:CH- synthonThe Journal of Organic Chemistry, 1978
- The Michael Type Alkylation of α,β-Unsaturated Sulfoxide and Reaction of the Resulting α-Sulfinyl CarbanionBulletin of the Chemical Society of Japan, 1978
- Erzeugung von und Olefinierung mit α‐S‐, ‐Se‐, ‐Si‐ und ‐Sn‐perheterosubstituierten (Trimethylsilyl)methyllithium‐VerbindungenEuropean Journal of Inorganic Chemistry, 1977
- A Useful Route for Olefin Synthesis: Thermolysis of the Michael Adducts of Aryl Vinyl SulfoxidesSynthesis, 1977
- Synthesis of alkenes from carbonyl compounds and carbanions alpha to silicon. III. Full report and a synthesis of the sex pheromone of gypsy mothThe Journal of Organic Chemistry, 1974
- .alpha.-Silylated vinyl ketones. New class of reagents for the annelation of ketonesJournal of the American Chemical Society, 1973