103563-41-3Relevant academic research and scientific papers
STEREOSELECTIVE SYNTHESIS OF C(1)-C(9) AND C(11)-C(17) FRAGMENTS OF PROTOMYCINOLIDE IV BASED ON ASYMMETRIC PINACOL-TYPE REARRANGEMENT
Suzuki, Keisuke,Tomooka, Katsuhiko,Matsumoto, Takashi,Katayama, Eiji,Tsuchihashi, Gen-ichi
, p. 3711 - 3714 (2007/10/02)
Two chiral intermediates, C(1)-C(9) and C(11)-C(17) portions of protomycinolide IV, were synthesized both from (S)-ethyl lactate via asymmetric pinacol-type rearrangement followed by diastereoselective reactions on α-methyl-β,γ-unsaturated carbonyl compounds.
