118-72-9Relevant articles and documents
CuI-nanoparticles-catalyzed selective synthesis of phenols, anilines, and thiophenols from aryl halides in aqueous solution
Xu, Hua-Jian,Liang, Yu-Feng,Cai, Zhen-Ya,Qi, Hong-Xia,Yang, Chun-Yan,Feng, Yi-Si
, p. 2296 - 2300 (2011/06/17)
CuI-nanoparticles-catalyzed selective synthesis of phenols, anilines, and thiophenols from aryl halides was developed in the absence of both ligands and organic solvents. Anilines were formed selectively with ammonia competing with hydroxylation and thiophenols were generated selectively with sulfur powder after subsequent reduction competing with hydroxylation and amination.
Copper-catalyzed coupling of thiourea with aryl iodides: The direct synthesis of aryl thiols
Qiao, Shu,Xie, Kun,Qi, Junsheng
scheme or table, p. 1441 - 1443 (2011/01/04)
A general, economical and efficient protocol for the direct copper-catalyzed coupling of thiourea with aryl iodides is developed and it will be potentially applied in large-scale industry as a preferred process.
A mild and practical deprotection method for benzyl thioethers
Akao, Atsushi,Nonoyama, Nobuaki,Yasuda, Nobuyoshi
, p. 5337 - 5340 (2007/10/03)
A highly effective and mild deprotection method was developed for benzyl thioethers using dibutylmagnesium in the presence of a catalytic amount of titanocene dichloride. This methodology is applicable to both aromatic and aliphatic benzyl thioethers.
Reductions using LiCl/NaBH4: A rapid and efficient cleavage of organic disulfides to mercaptans
Rajaram,Purushothama Chary,Iyengar
, p. 622 - 624 (2007/10/03)
A practical and novel reagent system LiCl/NaBH4 is used for the reductive cleavage of organic disulfides to mercaptans under mild conditions, in excellent yields.
A novel, practical and highly chemoselective methodology for reduction of disulphides to thiols
Vidya Sagar Reddy,Venkat Rao,Iyengar
, p. 859 - 862 (2007/10/03)
A novel, simple and efficient method for the reduction of disulfides to thiols using In/NH4Cl is described.
A rapid and efficient cleavage of organic disulfides to mercaptans using ZrCl4/NaBH4
Purushothama Chayr,Rajaram,Iyengar
, p. 3905 - 3911 (2007/10/03)
A practical and cheaper reagent system ZrCl/NaBH4 is used for the reductive cleavage of organic disulfides to mercaptans under mild conditions, in excellent yields.
β-carboxy sulfonamide ACAT inhibitors
-
, (2008/06/13)
β-Carboxy sulfonyl compounds of the formula STR1 wherein R1 is aryl, R3 is hydrogen or alkyl, R3 and R4 are hydrogen or alkyl, Y is --O--, --S--, or --NR2 --, and R5 is alkyl or aryl are potent inhibitors of the enzyme acyl CoA:cholesterol acyltransferase (ACAT) and are thus useful for treating hypercholesterolemia and atherosclerosis.