41987-22-8Relevant academic research and scientific papers
Direct synthesis of: N -sulfenylimines through oxidative coupling of amines with disulfides/thiols over copper based metal-organic frameworks
Long, Wei,Qiu, Wenge,Li, Chuanqiang,Song, Liyun,Bai, Guangmei,Zhang, Guizhen,He, Hong
, p. 40945 - 40952 (2016/05/19)
A highly porous metal-organic framework based on supramolecular building blocks with pcu-topology (pcu-MOF) has been tested for the oxidative coupling of amines and disulfides or thiols to afford the N-sulfenylimines directly in good yields without the fo
Copper-catalyzed oxidative N-S bond formation for the synthesis of N-sulfenylimines
Lee, Chan,Wang, Xi,Jang, Hye-Young
supporting information, p. 1130 - 1133 (2015/03/14)
Despite the remarkable success of the copper-catalyzed oxidative coupling reaction, direct cross-coupling of amines and thiols for the synthesis of N-sulfenylimines has not been previously reported. Using commercially available copper catalysts (CuI) and
Imino-Bridged Heterocycles. IV . A Facile Synthesis of Sulfenimines Derived from Diaryl Ketones
Brenner, Daniel G.,Cavolowsky, Kathleen Mensler,Shepard, Kenneth L.
, p. 805 - 808 (2007/10/02)
Efficient, high-yield syntheses of N-diarylmethylene sulfenamides (sulfenimines) have been developed under mild laboratory conditions.Diaryl ketones have been shown to form ketimines readily by condensation with ammonia in the presence of titanium tetrachloride.
A New Synthetic Method for Sulphenimines. Fluoride-catalysed Reaction of N,N-Bis(trimethylsilyl)sulphenamides with Aldehydes and Ketones
Morimoto, Toshiaki,Nezu, Yoshitaka,Achiwa, Kazuo,Sekiya, Minoru
, p. 1584 - 1585 (2007/10/02)
A convenient, general method for the preparation of sulphenimines by the reaction of aldehydes and ketones with N,N-bis(trimethylsilyl)sulphenamides in the presence of tetrabutylammonium fluoride catalyst is described.
Preparations of (Alkylideneamino)sulfonium Salts, Thioxime S-Alkyl Ethers, and of (Alkylideneamino) Thiocyanates
Reck, Reinhard,Jochims, Johannes C.
, p. 1494 - 1508 (2007/10/02)
Stable (alkylideneamino)sulfonium salts (1a - u) are obtained from α-halogen isocyanates (12) by reaction with sulfoxides (13), from the reaction of N-chloroimines (14) with sulfides (15), or by alkylation of N-alkylidenesulfenamides (16) with trimethylox
REACTION OF N-ARYLTHIO AND N-ARYLSULFINYLKETIMINES WITH CHLORINE. N-(1-CHLORO-1-PHENYL-2,2,2-TRIFLUOROETHYL)SULFINIMIDOYL AND N-(1-CHLORO-1-PHENYL-2,2,2-TRIFLUOROETHYL)SULFONIMIDOYL CHLORIDES
Shermolovich, Yu.G.,Talanov, V.S.,Dolenko, G.N.,Markovskii, L.N.
, p. 843 - 849 (2007/10/02)
N-Arylthio- and N-arylsulfinylphenyl trifluoromethyl ketimines react with chlorine to form N-(α-chloroalkyl)arenesulfinimidoyl and N-(α-chloralkyl)arenesulfonimidoyl chlorides.The reaction of N-phenylthiodiphenyl ketimine with chlorine gives the chlorosul
