Syntheses of β-hydroxyselenides and selenides from 1,2,3-selenadiazoles: Selenophilic reaction of phenylmagnesium bromide on α-selenoketones
Author:
Publisher
Wiley
Subject
Organic Chemistry
Reference12 articles.
1. Electrophilic and nucleophilic organoselenium reagents. New routes to .alpha.,.beta.-unsaturated carbonyl compounds
2. Organoselenium chemistry. .alpha.-Phenylseleno carbonyl compounds as precursors for .alpha.,.beta.-unsaturated ketones and esters
3. Modern organoselenium chemistry
4. Five-membered Selenium-Nitrogen Heterocycles
5. Transformation of α-phenylseleneketones to allylic selenides via migration of the phenylseleno group
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1. Preparation of 2-Arylethynylselanylacetonitriles from 4-Aryl-1,2,3-selenadiazoles;Journal of Heterocyclic Chemistry;2014-06-24
2. Volume 4 References;Comprehensive Heterocyclic Chemistry II;1996
3. Three or Four Heteroatoms including at least One Selenium or Tellurium;Comprehensive Heterocyclic Chemistry II;1996
4. Vicinal Difunctionalization of Alkynyl Selenides with Lithium Butylcyano Cuprate and Electrophiles;Synthetic Communications;1994-04
5. Preparation of β-hydroxysulfides from 1,2,3-thiadiazoles. Comparison of the effect of phenylmagnesium bromide on α-Thio- and α-selenoketones;Journal of Heterocyclic Chemistry;1990-11
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