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
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.
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.
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
