Features of the intramolecular Hosomi–Sakurai reaction of allylic cyclopentenylsilane containing an enol ether moiety
Authors:
- Airat M. GimazetdinovAGAirat M. Gimazetdinov
- Mansur S. MiftakhovMMMansur S. Miftakhov
- 31 May 2023
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 123
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Fluoride anion-induced intramolecular cyclopropanation of allylsilanesTetrahedron Letters, 2017
- A simple and efficient synthesis of enantiomeric (3aRS,4RS,6aSR)-4-hydroxy-3,3a,4,6a-tetrahydro-1H-cyclopenta[c]furan-1-onesTetrahedron, 2012
- Regulation of Nrf2-dependent gene expression by 15-deoxy-Δ12,14-prostaglandin J2Free Radical Biology and Medicine, 2009
- Selective reactions using allylic metalsChemical Reviews, 1993
- Preparation of bicyclo[5.3.0]decan-1-ols from the tandem anionic oxy-Cope rearrangement/allylsilane cyclization of 1,2-divinylcyclohexanolsThe Journal of Organic Chemistry, 1990
- Intramolecular Addition Reactions of Allylic and Propargylic SilanesSynthesis, 1988
- On the stereochemistry of allylmetal‐aldehyde condensations. Preliminary communicationHelvetica Chimica Acta, 1983
- Chemistry of organosilicon compounds 113 chemoselective allylation of carbonyl compounds with allylsilanes promoted by tetra--butylammonium fluoride. A new synthesis of homoallyl alcoholsTetrahedron Letters, 1978