Stereospecific cyclopropane synthesis from γ-stannyl alcohols
- 16 April 1985
- journal article
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 285 (1-3) , 173-191
- https://doi.org/10.1016/0022-328x(85)87366-6
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Stereospecific cyclopropane synthesis from γ-stannyl alcoholsTetrahedron Letters, 1983
- β-Stannylpropionaldehyde. A versatile cyclopropane building-blockTetrahedron Letters, 1982
- Carbonium ion rearrangements controlled by the presence of a silyl groupTetrahedron Letters, 1981
- Polar Substituent Effects in the Solvolysis of Acyclic Tertiary Chlorides Polar Effects VIHelvetica Chimica Acta, 1979
- Die Solvoyse von 4‐substituierten 2‐Chlor‐2‐methylbutanenHelvetica Chimica Acta, 1979
- Kinetics of cyclopropane formation by 1,3-deoxystannylation. A kinetic isotope effect as a probe for the mechanism of neighboring group participationJournal of the American Chemical Society, 1978
- Deoxymetalation reactions. The concerted nature of 1,3-DeoxystannylationJournal of Organometallic Chemistry, 1974
- Stereospecific cyclopropane-ring formation by 1,3-deoxymetalation of trimethyltin-substituted norbornyl mesylatesJournal of the American Chemical Society, 1974
- Electrophilically-induced cyclodestannylation reactionsJournal of Organometallic Chemistry, 1974
- Deoxymetalations. 1,3 eliminations of organotin alcoholsJournal of Organometallic Chemistry, 1970