| Literature DB >> 20077541 |
Charles Fehr1, Andrea K Buzas, Oliver Knopff, Jean-Yves de Saint Laumer.
Abstract
(+)-(R,Z)-5-Muscenone ((R)-1) was synthesized by an enantioselective aldol reaction, catalyzed by new ephedrine-type Ti reagents (up to 70 % enantiomeric excess). Substrate-directed diastereoselective reduction of the aldol product and Grob fragmentation of the tosylate of the resultant 1,3-diol afforded (+)-1. This approach also gave access to (-)-(R,E)-5-muscenone and (-)-(R)-muscone.Entities:
Year: 2010 PMID: 20077541 DOI: 10.1002/chem.200902774
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236