Bulletin of the Chemical Society of Japan p. 1763 - 1767 (1996)
Update date:2022-08-05
Topics:
Uno, Hidemitsu
Oka, Kenji
Tani, Hiroyuki
Kawada, Yoshihiro
Ono, Noboru
1-Phenylsulfanyl-2,2,2-trifluoroethyl isocyanide (2a) readily and selectively trimerized to 4,6-bis(phenylsulfanyl)-1-(1-phenylsulfanyl-2,2,2-trifluoroethyl)-5-(2,2,2- trifluoroethylideneamino)-2-trifluoromethyl-1,2-dihydropyrimidine (5) at room temperature, while other α-phenylsulfanyl isocyanides such as phenyl(phenylsulfanyl)methyl isocyanide (2b) are stable. Heating of 2b resulted in formation of the corresponding nitrile as well as diphenyl disulfide and [bis(phenylsulfanyl)methyl]benzene.
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Doi:10.1039/cc9960001615
(1996)Doi:10.1080/00397919608004629
(1996)Doi:10.1021/om960150b
(1996)Doi:10.1021/om9602320
(1996)Doi:10.1016/0040-4039(96)01117-3
(1996)Doi:10.1002/jhet.5570330304
(1996)