Abstract
Dimethyl sulfoxide and a variety of other highly polar solvents are shown to promote both inter- and intramolecular cyclopentenone formation from alkenes and (alkyne)hexacarbonyldicobalt complexes. Their use leads to significant changes in both regio- and stereoselectivity when compared to other reaction conditions.
Original language | English |
---|---|
Pages (from-to) | 220-223 |
Number of pages | 4 |
Journal | Organometallics |
Volume | 12 |
Issue number | 1 |
DOIs | |
Publication status | Published - 1993 |
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry