Reductive cleavage of Se - Si bond in arylselenotrimethylsilane: A novel method for the synthesis of selenoesters

DOI: 10.1080/00397919808004959

Source and publish data:

Synthetic Communications p. 3999 - 4002 (1998)

Update date:2022-08-16

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Authors:

Zhang Zhang

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Article abstract of DOI:10.1080/00397919808004959

Arylselenotrimethylsilane is reduced by samarium diiodide to yield samarium arylselenolates. These new selenolate anion species reacted smoothly with acyl halides to give selenoesters.

Full text of DOI:10.1080/00397919808004959

Synthetic Communications

ISSN: 0039-7911 (Print) 1532-2432 (Online) Journal homepage: http://www.tandfonline.com/loi/lsyc20

Reductive Cleavage of Se–Si Bond in

Arylselenotrimethylsilane: A Novel Method for the

Synthesis of Selenoesters

Songlin Zhang & Yongmin Zhang

To cite this article: Songlin Zhang & Yongmin Zhang (1998) Reductive Cleavage of Se–Si Bond

in Arylselenotrimethylsilane: A Novel Method for the Synthesis of Selenoesters, Synthetic

Communications, 28:21, 3999-4002, DOI: 10.1080/00397919808004959

To link to this article: http://dx.doi.org/10.1080/00397919808004959

Published online: 16 Aug 2006.

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