The 16th Iranian chemistry congress

Croatica Chemica Acta, 2014

Arkivoc, 2015

Mini-Reviews in Medicinal Chemistry, 2014

Asian Journal of Chemistry, 2019

European Journal of Organic Chemistry, 2009

We have developed a general economical and environmentally benign method for the preparation of isothiocyanates from the corresponding dithiocarbamic acid salts by using cheap and readily available reagent molecular iodine. This is perhaps the most efficient method reported so far for the synthesis of isothiocyanates. The reagent is easily available and nontoxic, and the precipitated sulfur can be removed easily; hence, this method is most suitable for large-scale synthesis.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

Synthesis, 2017

A number of alkyl, aryl and bifunctional isothiocyanates are obtained in moderate to high yields (41–94%) in a two-step, one-pot reaction of the parent primary amines or their salts with carbon disulfide, followed by reaction of the thus formed dithiocarbamates with T3P® (propane phosphonic acid anhydride) as a new and efficient desulfurating agent.

ChemInform, 2000

Chinese Journal of Chemistry, 2008

Synthetic Communications, 2016

Synthetic Communications, 2010