Tetrahedron letters

Preparation of Np-tosylaldimines by the intramolecular photo-imino group migration of naphtho [1, 8-de] dithiin-1-N-tosylsulfilimines

T Fujii, T Kimura, N Furukawa

Index: Fujii, Takayoshi; Kimura, Takeshi; Furukawa, Naomichi Tetrahedron Letters, 1995 , vol. 36, # 7 p. 1075 - 1078

Full Text: HTML

Citation Number: 23

Abstract

Naphth [1, 8-de] dithiin-1-N-tosylsulfilimines (4) were prepared by the reaction of naphtho [1, 8-de] dithiins with chloramine-T. Photolysis of 4 undergoes intramolecular imino group rearrangement to give N-tosylaldimines quantitatively together with naphthalene-1, 8- dithiole.

Related Articles:

Hydrocyanation of sulfonylimines using potassium hexacyanoferrate (II) as an eco-friendly cyanide source

[Li, Zheng; Li, Rongzhi; Zheng, Huanhuan; Wen, Fei; Li, Hongbo; Yin, Junjun; Yang, Jingya Journal of the Brazilian Chemical Society, 2013 , vol. 24, # 11 p. 1739 - 1743]

A new method for preparation of 3, 6-dihydro-2H-1, 3-oxazines and explorations of their use in stereoselective synthesis of 1, 3-amino alcohol derivatives

[Cherkauskas, John P.; Klos, Andrew M.; Borzilleri, Robert M.; Sisko, Joseph; Weinreb, Steven M.; Parvez, Masood Tetrahedron, 1996 , vol. 52, # 9 p. 3135 - 3152]

More Articles...