Phosphine-free conversion of alcohols into alkyl thiocyanates using trichloroisocyanuric acid/NH4SCN
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference29 articles.
1. Trichloroisocyanuric Acid: A Safe and Efficient Oxidant
2. A simple synthesis of 1-thiophenoxy-3-chloroalkenes useful synthons for acrolein and methacrolein
3. H. Suzuki, Japanese Patent 09067359 A2, Chem. Abstr. 126 (1997) 277382.
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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. A Simple, One-Pot and Phosphine-Free Procedure for Thiocyanation of Alcohols Using N-(p-toluenesulfonyl) Imidazole (TsIm);Journal of Chemical Research;2016-10
3. 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
4. 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
5. Selectfluor™ F-TEDA-BF4 mediated thiocyanation or isothiocyanation of alcohols by in situ generation of [+SCN] under heterogeneous and neutral conditions;Journal of Fluorine Chemistry;2012-05
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