Tetrahedron Letters

A one-pot, three-component synthesis of thiazolidine-2-thiones

A Ziyaei-Halimehjani, K Marjani, A Ashouri

Index: Ziyaei-Halimehjani, Azim; Marjani, Katayoun; Ashouri, Akram Tetrahedron Letters, 2012 , vol. 53, # 27 p. 3490 - 3492

Full Text: HTML

Citation Number: 15

Abstract

An efficient method for the synthesis of thiazolidine-2-thiones is described via regiospecific iodocyclization of an allyl amine, carbon disulfide, and iodine. Dehydrohalogenation of the iodo-derivatives gives thiazole-2 (3H)-thiones. In addition, nucleophilic substitution of the iodine in the products is accomplished using NaN3, thiophenol, or dithiocarbamate.

Related Articles:

Electron transfer induced ring opening of 2-(bromomethyl) aziridines by magnesium in methanol

[Tehrani, Kourosch Abbaspour; NguyenVan, Tuyen; Karikomi, Michinori; Rottiers, Mario; De Kimpe, Norbert Tetrahedron, 2002 , vol. 58, # 35 p. 7145 - 7152]

Electron transfer induced ring opening of 2-(bromomethyl) aziridines by magnesium in methanol

[Tehrani, Kourosch Abbaspour; NguyenVan, Tuyen; Karikomi, Michinori; Rottiers, Mario; De Kimpe, Norbert Tetrahedron, 2002 , vol. 58, # 35 p. 7145 - 7152]

Electron transfer induced ring opening of 2-(bromomethyl) aziridines by magnesium in methanol

[Tehrani, Kourosch Abbaspour; NguyenVan, Tuyen; Karikomi, Michinori; Rottiers, Mario; De Kimpe, Norbert Tetrahedron, 2002 , vol. 58, # 35 p. 7145 - 7152]

Highly enantioselective intermolecular hydroamination of allylic amines with chiral aldehydes as tethering catalysts

[MacDonald, Melissa J.; Hesp, Colin R.; Schipper, Derek J.; Pesant, Marc; Beauchemin, Andre M. Chemistry - A European Journal, 2013 , vol. 19, # 8 p. 2597 - 2601]

More Articles...