41866-62-0Relevant academic research and scientific papers
A metal-free and recyclable synthesis of benzothiazoles using thiourea as a sulfur surrogate
Yin, Yan,Zhou, Hong,Liu, Xichen,Chen, Haiying,Wu, Fanhong,Zhang, Heng,Tao, Ruiheng,Cheng, Fengkai,Feng, Yangbo
, p. 1709 - 1712 (2015/03/14)
Using odorless thiourea as the S source, benzothiazoles and asymmetric disulfides could be obtained from thioformanilides through the tandem cyclization/nucleophilic addition/hydrolysis/nucleophilic substitution reaction. Furthermore, the obtained asymmetric disulfides could readily transfer to benzothiazoles after nitro-reduction and amide formation reaction. This metal-free and recyclable synthetic methodology offered a time-efficient, less expensive, and environmentally friendly alternative to multifunctional benzothiazoles.
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.
