56430-88-7Relevant articles and documents
Mild and efficient method for-thiocyanation of ketones and-dicarbonyl compounds using bromodimethylsulfonium bromide-ammonium thiocyanate
Bhalerao, Dinesh S.,Akamanchi, Krishnacharya G.
, p. 799 - 807 (2010)
An efficient and convenient method for-thiocyanation of ketones and-dicarbonyl compounds has been developed using a reagent combination of bromodimethylsulfonium bromide (BDMS) and ammonium thiocyanate in acetonitrile. The developed method is mild and gave good yield of the products at room temperature.
Heteropoly acids as heterogeneous and reusable catalyst for α-thiocyanation of ketones
Chaskar, Atul C.,Yadav, Arun A.,Langi, Bhushan P.,Murugappan, Anita,Shah, Chetan
experimental part, p. 2850 - 2856 (2010/10/20)
Simple, efficient, and mild method for -thiocyanation of ketones in presence of heteropolyacid has been developed. This methodology offered -oxothiocyanates in good to excellent yields at room temperature in a highly selective manner. The catalyst could b
Iron(III) chloride as mild and efficient reagent for the α-thiocyanation of ketones: An expedient synthesis of α-oxo thiocyanates
Yadav, Jhillu S.,Subba Reddy, Basi V.,Subba Reddy, Ummareddy V.,Chary, Darshanoju N.
, p. 1283 - 1287 (2008/12/22)
A simple and efficient method for the α-thiocyanation of ketones has been developed; anhydrous iron(III) chloride is used under mild conditions to produce αoxo thiocyanates in good to high yields and with high selectivity. The use of inexpensive and readi