Abstract
Symmetrical Z,Z-bis(1-hydroxymethyl-2-chlorovinyl) selenides have been obtained in high yields by regio- and stereospecific addition of selenium dichloride to propargylic alcohols. Presumably, the hydroxyl group plays an important role in the regio- and stereospecific addition.
Original language | English |
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Pages (from-to) | 2663-2666 |
Number of pages | 4 |
Journal | Synlett |
Issue number | 17 |
DOIs | |
State | Published - 16 Oct 2007 |
Keywords
- Alkynes
- Divinyl diselenides
- Divinyl selenides
- Electrophilic addition
- Regioselectivity
- Selenium
- Stereoselectivity