Application of N-thiocyanatosuccinimide as a reagent for the facile conversion of epoxides into thiocyanohydrines
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference45 articles.
1. A Versatile Procedure for the Preparation of Aryl Thiocyanates Using N-Thiocyanatosuccinimide (NTS)
2. Facile Ring-Expansion Substitution Reactions of 1,3-Dithiolanes and 1,3-Dithianes Initiated by Electrophilic Reagents to Produce Monohalo-, -cyano-, -azido- and -thiocyanato-1,4-dithiins and -1,4-dithiepins
3. Electrophilic α-thiocyanation of chiral and achiral N-acyl imides. A convenient route to 5-substituted and 5,5-disubstituted 2,4-thiazolidinediones
4. An efficient and catalytically enantioselective route to (S)-(-)-phenyloxirane
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1. Phosphine-free Direct Conversion of Carboxylic Acids into Acyl Isothiocyanates Using Various Electrophilic Halogenation Reagents;Letters in Organic Chemistry;2018-07-26
2. Nucleophilic ring-opening of epoxides: trends in β-substituted alcohols synthesis;Journal of the Iranian Chemical Society;2018-05-28
3. Direct thiocyanation of ketene dithioacetals under transition-metal-free conditions;Organic Chemistry Frontiers;2017
4. 2,4,4,6-Tetrabromo-2,5-cyclohexadienone as an efficient reagent for phosphine-free electrophilic transformation of alcohols and epoxides;J SULFUR CHEM;2016
5. Remarkably Fast and Mild Solvent-Free Conversion of Epoxides into Thiocyanohydrins Using Mukaiyama Reagent;Phosphorus, Sulfur, and Silicon and the Related Elements;2012-08-06
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