175551-72-1Relevant articles and documents
De novo formal synthesis of (-)-virginiamycin M2 via the asymmetric hydration of dienoates
Mortensen, Matthew S.,Osbourn, Joshua M.,O'Doherty, George A.
, p. 3105 - 3108 (2008/02/10)
A de novo approach to the formal total synthesis of the macrolide natural product (-)-virginiamycin M2 has been achieved via a convergent approach. The absolute and relative stereochemistry of the nonpeptide portion of (-)-virginiamycin M2