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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 24, 1994 - Issue 10
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Original Articles

Aromatic Nucleophilic Substitution by Arylselenolate Ions Produced Through Reductive Cleavage of Diaryl Diselenide Induced by SmI2-THF-HMPA System

Weiliang Bao Department of Chemistry, Hangzhou University, Hangzhou, 310028, the People's Republic of China
,
Yongmin Zhang Department of Chemistry, Hangzhou University, Hangzhou, 310028, the People's Republic of China
&
Shuangwei Chen Department of Chemistry, Hangzhou University, Hangzhou, 310028, the People's Republic of China
Pages 1339-1343 | Received 26 Oct 1993, Published online: 23 Sep 2006
 
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Abstract

Arylselenolate Ions which were produced through reductive cleavage of Se-Se bond in diaryl diselenide undergo nucleophilic substitution on aromatic rings and a series of new unsymmetrical diaryl selenides were synthesized.

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