Protonation, and reductive cleavage by lithium of the CS bond, in (methylthio)pentadienylic anions generated from various cis,trans-isomers of 1-(methylthio)-1,3-pentadiene and 1-(methylthio)-1,4-pentadiene-Reference-Cited by-同舟云学术

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Protonation, and reductive cleavage by lithium of the CS bond, in (methylthio)pentadienylic anions generated from various cis,trans-isomers of 1-(methylthio)-1,3-pentadiene and 1-(methylthio)-1,4-pentadiene

Published:2010-09-02 Issue:10 Volume:101 Page:346-351
ISSN:0165-0513
Container-title:Recueil des Travaux Chimiques des Pays-Bas
language:en
Short-container-title:Recl. Trav. Chim. Pays-Bas

Author:

Gräfing R.,George A. V. E.,Brandsma L.

Publisher

Wiley

Subject

General Chemistry

Reference15 articles.

1. Chemistry of 2H-thiopyran and derivatives IV. Deprotonation and methylation of 2H-thieno[2,3-b]thiopyran and some derivatives

2. 2-Alkenyl anions and their surprising endo preference. Facile and extreme stereocontrol over carbon-carbon linking reactions with organometallics of the allyl type

3. G. Boche D. R. Schneider Tetrahedron Lett 3657 1976

4. NMR spectra and configuration of some methylallylic anions

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1. Sodium-Hexamethylphosphoric triamide;Fieser and Fieser's Reagents for Organic Synthesis;2006-12-15

2. Conjugated methyl sulfide and phenyl sulfide derivatives of oxidosqualene as inhibitors of oxidosqualene and squalene-hopene cyclases;Lipids;2003-03

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