78985-17-8Relevant academic research and scientific papers
One-pot reductive sulfenylation and thiocyanation of carbonyl compounds in ionic liquid media
Yadav, Lal Dhar S.,Garima,Kapoor, Ritu
, p. 100 - 112 (2011/03/17)
The first example of an efficient one-pot reductive sulfenylation and thiocyanation of carbonyl compounds in environmentally benign ionic liquid (IL) media is reported. The process involves reduction of carbonyl compounds with NaBH4 in the IL [bmim]BF4 followed by I2-catalyzed reaction of the resulting alcohols with aromatic/aliphatic thiols or ammonium thiocyanate in the same vessel to afford sulfides or thiocyanates, respectively, in excellent yields (78-93%). Notably, the protocol precludes the necessity to prepare and isolate the intermediate alcohols in a separate step as they are formed in situ, and the IL used can be recycled easily for further use without any loss of efficiency. Copyright
A novel approach to the practical synthesis of sulfides: An InBr 3-Et3SiH catalytic system promoted the direct reductive sulfidation of acetais with disulfides
Sakai, Norio,Moritaka, Kohei,Konakahara, Takeo
supporting information; experimental part, p. 4123 - 4127 (2009/12/09)
We have demonstrated a facile and direct synthesis of sulfide derivatives using acetais and ketals, derived, from aromatic/ conjugated, aldehydes and aromatic ketones, with disulfides and the InBr3-Et3SiH reducing system., We also succeeded in developing an unprecedented one-pot preparation of an aliphatic sulfide from a disulfide and an aliphatic acetal. (Wiley-VCH Verlag GmbH & Co. KGaA.
DIRECT CONVERSION OF BENZYL ALCOHOLS INTO BENZYL SULFIDES WITH ORGANIC DISULFIDE/DIPHOSPHORUS TETRAIODIDE
Suzuki, Hitomi,Sato, Naofumi
, p. 267 - 268 (2007/10/02)
Organic disulfides react with diphosphorus tetraiodide in hot benzene to give an orange-colored solution, in which benzyl alcohols are readily converted into the corresponding benzyl sulfides in fair to good yields.
