Abstract
The alkyne, 4, prepared stereoselectively in 7 steps from acetyl furan, reacts with (methoxy)(phenyl)carbenepentacarbonylchromium(0), 15, to give the model (16) for nogalarol (1b) in 43% yield.
Original language | English |
---|---|
Pages (from-to) | 605-608 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 31 |
Issue number | 5 |
DOIs | |
Publication status | Published - 1990 |
Externally published | Yes |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry