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 | |
| State | Published - Aug 2003 |
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Keywords
- (Z)-1,2-bis(Benzylseleno)ethane
- 1,4-Diselenin
- Dibenzyl selenide
- Selenophene
ASJC Scopus subject areas
- Inorganic Chemistry
- Chemistry(all)
Cite this
Unexpected reaction of (Z)-1,2-bis(benzylseleno)-ethene : The formation of 1,4-diselenin. / Potapov, Vladimir A.; Amosova, Svetlana V.; Doron'kina, Irina V.; Glass, Richard S.
In: Sulfur Letters, Vol. 26, No. 4, 08.2003, p. 137-140.Research output: Contribution to journal › Article
}
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 -