Synthetic communications

Odorless thioacetalization reagent 2??[1, 3] dithian??2??ylidene??3??oxo??butanamide and its chemoselectivity

J Liu, Q Liu, H Yu, Y Ouyang, D Dong

Index: Liu, Jun; Liu, Qun; Yu, Haifeng; Ouyang, Yan; Dong, Dewen Synthetic Communications, 2004 , vol. 34, # 24 p. 4545 - 4556

Full Text: HTML

Citation Number: 16

Abstract

Abstract 2??[1, 3] Dithian/dithiolan??2??ylidene??3??oxo??butanamide 2a/2b were synthesized and investigated in the thioacetalization reaction of aldehydes/ketones 3. The experiments revealed that 2a could be used as a nonthiolic, odorless 1, 3??propanedithiol equivalent in the conversion of aldehydes/ketones into the corresponding dithianes 4, however, 2b was less effective. Moreover, the chemoselectivity of the thioacetalization of 3 in the presence ...

Related Articles:

An efficient, continuous flow technique for the chemoselective synthesis of thioacetals

[Wiles, Charlotte; Watts, Paul; Haswell, Stephen J. Tetrahedron Letters, 2007 , vol. 48, # 41 p. 7362 - 7365]

α, α-diacetyl cyclic ketene dithioacetals: Odorless and efficient dithiol equivalents in thioacetalization reactions

[Yu, Haifeng; Liu, Qun; Yin, Yanbing; Fang, Qunxin; Zhang, Jingping; Dong, Dewen Synlett, 2004 , # 6 p. 999 - 1002]

More Articles...