Unexpected reaction of (Z)-1,2-bis(benzylseleno)-ethene: The formation of 1,4-diselenin

Vladimir A. Potapov; Svetlana V. Amosova; Irina V. Doron'kina; Richard S. Glass

doi:10.1080/0278611031000138018

Unexpected reaction of (Z)-1,2-bis(benzylseleno)-ethene: The formation of 1,4-diselenin

Vladimir A. Potapov, Svetlana V. Amosova, Irina V. Doron'kina, Richard S. Glass

Chemistry and Biochemistry

Research output: Contribution to journal › Article › peer-review

3 Scopus citations

Abstract

Heating (Z)-1,2-bis(benzylseleno)ethene at 140-180 °C leads to 1,4-diselenin (79% yield) and dibenzyl selenide. This unusual reaction represents a convenient method for preparing 1,4-diselenin.

Original language	English (US)
Pages (from-to)	137-140
Number of pages	4
Journal	Sulfur Letters
Volume	26
Issue number	4
DOIs	https://doi.org/10.1080/0278611031000138018
State	Published - Aug 2003

Keywords

(Z)-1,2-bis(Benzylseleno)ethane
1,4-Diselenin
Dibenzyl selenide
Selenophene

ASJC Scopus subject areas

Chemistry(all)
Inorganic Chemistry

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10.1080/0278611031000138018

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title = "Unexpected reaction of (Z)-1,2-bis(benzylseleno)-ethene: The formation of 1,4-diselenin",

abstract = "Heating (Z)-1,2-bis(benzylseleno)ethene at 140-180 °C leads to 1,4-diselenin (79% yield) and dibenzyl selenide. This unusual reaction represents a convenient method for preparing 1,4-diselenin.",

keywords = "(Z)-1,2-bis(Benzylseleno)ethane, 1,4-Diselenin, Dibenzyl selenide, Selenophene",

author = "Potapov, {Vladimir A.} and Amosova, {Svetlana V.} and Doron'kina, {Irina V.} and Glass, {Richard S.}",

year = "2003",

month = aug,

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language = "English (US)",

volume = "26",

pages = "137--140",

journal = "Journal of Sulfur Chemistry",

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T1 - Unexpected reaction of (Z)-1,2-bis(benzylseleno)-ethene

T2 - The formation of 1,4-diselenin

AU - Potapov, Vladimir A.

AU - Amosova, Svetlana V.

AU - Doron'kina, Irina V.

AU - Glass, Richard S.

PY - 2003/8

Y1 - 2003/8

N2 - Heating (Z)-1,2-bis(benzylseleno)ethene at 140-180 °C leads to 1,4-diselenin (79% yield) and dibenzyl selenide. This unusual reaction represents a convenient method for preparing 1,4-diselenin.

AB - Heating (Z)-1,2-bis(benzylseleno)ethene at 140-180 °C leads to 1,4-diselenin (79% yield) and dibenzyl selenide. This unusual reaction represents a convenient method for preparing 1,4-diselenin.

KW - (Z)-1,2-bis(Benzylseleno)ethane

KW - 1,4-Diselenin

KW - Dibenzyl selenide

KW - Selenophene

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DO - 10.1080/0278611031000138018

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EP - 140

JO - Journal of Sulfur Chemistry

JF - Journal of Sulfur Chemistry

SN - 1741-5993

IS - 4

ER -

Unexpected reaction of (Z)-1,2-bis(benzylseleno)-ethene: The formation of 1,4-diselenin

Abstract

Keywords

ASJC Scopus subject areas

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