709-94-4Relevant academic research and scientific papers
Stannous chloride-promoted synthesis of S-allyl-N-aryl dithiocarbamates under solvent-free conditions
Singh, Okram Mukherjee,Devi, Nepram Sushuma
experimental part, p. 516 - 522 (2011/04/19)
A highly efficient method of synthesis of S-allyl-N-aryl dithiocarbamates using SnCl2 as a catalyst under solvent-free conditions is described. The mild reaction conditions, high yields, and shorter reaction period illustrate the good synthetic utility of
Regiospecific iodocyclization of S-allyl dithiocarbamates: synthesis of 2-imino-1,3-dithiolane and 2-iminium-1,3-dithiolane derivatives
Halimehjani, Azim Ziyaei,Maleki, Hajar,Saidi, Mohammad R.
scheme or table, p. 2747 - 2749 (2009/09/25)
4-Alkyl-2-imino-1,3-dithiolanes and 4-alkyl-2-iminium-1,3-dithiolanes were prepared in excellent yields with complete regiospecificity under mild conditions by the iodocyclization of S-allyl dithiocarbamates. Dehydrohalogenation of the 4-alkyl-2-imino-1,3
Palladium-catalyzed hetero-cope rearrangement of alkyl allyl N-aryldithiocarbonimidates
Garin,Melendez,Merchan,Tejero,Uriel,Ayestaran
, p. 147 - 149 (2007/10/02)
Palladium-catalyzed [3,3] sigmatropic rearrangement of allyl methyl N-aryldithiocarbonimidates affords methyl N-allyl-N-aryldithiocarbamates. Very high yields of rearranged products can be obtained depending on the substitution pattern of the allyl group.
