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

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
Publication status	Published - Aug 2003

Fingerprint

Keywords

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

ASJC Scopus subject areas

Inorganic Chemistry
Chemistry(all)

Cite this

Potapov, V. A., Amosova, S. V., Doron'kina, I. V., & Glass, R. S. (2003). Unexpected reaction of (Z)-1,2-bis(benzylseleno)-ethene: The formation of 1,4-diselenin. Sulfur Letters, 26(4), 137-140. https://doi.org/10.1080/0278611031000138018

@article{45e9a9f4f5d9495eb6d23561ef8666b2,

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 = "8",

doi = "10.1080/0278611031000138018",

language = "English (US)",

volume = "26",

pages = "137--140",

journal = "Journal of Sulfur Chemistry",

issn = "1741-5993",

publisher = "Taylor and Francis Ltd.",

number = "4",

}

TY - JOUR

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

UR - http://www.scopus.com/inward/record.url?scp=0346024246&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0346024246&partnerID=8YFLogxK

U2 - 10.1080/0278611031000138018

DO - 10.1080/0278611031000138018

M3 - Article

AN - SCOPUS:0346024246

VL - 26

SP - 137

EP - 140

JO - Journal of Sulfur Chemistry

JF - Journal of Sulfur Chemistry

SN - 1741-5993

IS - 4

ER -

Access to Document

10.1080/0278611031000138018