130705-40-7Relevant articles and documents
A STEREOSELECTIVE OSMYLATION APPROACH TO POLYOXYGENATED NATURAL PRODUCTS. SYNTHESIS OF C(1)-C(7) AND C(7)-C(13) SUBUNITS OF ERYTHRONOLIDE A
Kim, Young Gyu,Whang, Konghyun,Cooke, R. J.,Cha, Jin K.
, p. 3275 - 3278 (2007/10/02)
The key synthons 2 and 3 of the erythronolide A seco acid (1) have been prepared in an enantiomerically pure form, utilizing a stereoselective osmylation of chiral hydroxy (Z,E)-diene ester 6a and subsequent hydrogenation