New mechanistic aspects on the catalytic transformation of vinylthiiranes to mono and disubstituted 3,6-dihydro-1,2-dithiins by tungsten pentacarbonyl monoacetonitrile-Reference-Cited by-同舟云学术

New mechanistic aspects on the catalytic transformation of vinylthiiranes to mono and disubstituted 3,6-dihydro-1,2-dithiins by tungsten pentacarbonyl monoacetonitrile

Published:2002-05 Issue:22 Volume:58 Page:4517-4527
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Lupton David W,Taylor Dennis K

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference33 articles.

1. New synthetic methodology utilising 1,2-dioxines and stabilised phosphorus ylides: a highly diastereoselective cyclopropanation reaction

2. A New Route to Diastereomerically Pure Cyclopropanes Utilizing Stabilized Phosphorus Ylides and γ-Hydroxy Enones Derived from 1,2-Dioxines: Mechanistic Investigations and Scope of Reaction

3. Exploitation of ylide steric bulk to alter cyclopropanation outcome during the reaction of 1,2-dioxines and stabilised phosphorus ylides

4. Mechanistic Investigations on the Reaction between 1,2-Dioxines and Bulky Stabilized Phosphorus Ylides: An Efficient Route to Closely Related Cyclopropane Stereoisomers

5. Molecular sulfur (S2): generation and synthetic application

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