111820-86-1Relevant articles and documents
An Enantioselective Synthesis of a Macrolide from the Polyketide Lactone Derived from Oleandomycin
Tatsuta, Kuniaki,Kobayashi, Yoshiyuki,Akimoto, Kohji,Kinoshita, Mitsuhiro
, p. 187 - 190 (1987)
The polyketide lactone, 8-methyl-3,5,11-trioxo-oleandolide, which is obtained from a new aglycone of oleandomycin by ruthenium tetraoxide oxidation, is stereoselectively reduced by zinc borohydride in the presence of magnesium bromide to give a macrolide,