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Paper | Regular issue | Vol 45, No. 3, 1997, pp.575-584
Published online, 1st January, 1970
DOI: 10.3987/COM-96-7719
Synthesis of Cyclic Halooxatelluranes via Dehalogenation of α-Halo Carbonyl Compounds with Tellurides Containing Hydroxy Group on Side Chain

Jian Zhang, Shinichi Saito, Tamiko Takahashi, and Toru Koizumi*

*Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, 2630 Sugitani, Toyama, Toyama 930-0194, Japan

Abstract

The synthesis of cyclic halooxatelluranes (3a, 4a-d, 5a) has been achieved via dehalogenation of α-halo carbonyl compounds (2A-F) with tellurides (1a-d) containing hydroxy group on the side chain. Halophilicity of the tellurides was compared with that of selenides and a plausible reaction mechanism is discussed.