Synlett 2004(6): 999-1002  
DOI: 10.1055/s-2004-822892
LETTER
© Georg Thieme Verlag Stuttgart · New York

α,α-Diacetyl Cyclic Ketene Dithioacetals: Odorless and Efficient Dithiol Equivalents in Thioacetalization Reactions

Haifeng Yu, Qun Liu*, Yanbing Yin, Qunxin Fang, Jingping Zhang, Dewen Dong*
Department of Chemistry, Northeast Normal University, Changchun, 130024, P. R. China
Fax: +86(431)5268966; e-Mail: dongdw663@nenu.edu.cn;
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Publikationsverlauf

Received 24 February 2004
Publikationsdatum:
25. März 2004 (online)

Abstract

Two novel, non-thiolic, odorless dithiol equivalents, α,α-diacetyl cyclic ketene dithioacetals 2a and 2b, had been developed. A range of carbonyl compounds 3 were converted into corresponding dithioacetals, dithianes 4 and dithiolanes 5, in high yields (up to 99%) in the presence of 2a or 2b. Moreover, 2a and 2b show high chemoselectivity between aldehyde and ketone in thioacetalization.

10

All dithioacetals 4, 5 and 9 prepared in the present work are known compounds and were identified by 1H NMR, IR spectroscopy and elemental analyses, the data for these compounds are in good agreement with that in literatures.