765300-72-9Relevant academic research and scientific papers
Total synthesis of aculeatins A and B from (S)-malic acid
Kamal, Ahmed,Reddy, Papagari Venkat,Prabhakar, Singanaboina,Balakrishna, Moku
experimental part, p. 2861 - 2865 (2010/04/02)
A simple convergent approach towards the total synthesis of bioactive spiroacetals aculeatins A and B is described. The key features of the synthetic strategy include a syn-stereoselective 1,3-asymmetric reduction, epoxide ring opening and oxidative spiro
Total synthesis of xestodecalactone c from L-malic acid
Yadav,Rao, Y. Gopala,Ravindar,Reddy, B. V. Subba,Narsaiah
body text, p. 3157 - 3161 (2009/12/27)
An efficient total synthesis of the ten-membered macrolide, xestodecalactone C is described. The synthetic sequence uses Barbier-allylation, LiAlH4/LiI-mediated syn-stereoselective 1,3-asymmetric reduction, and intramolecular Friedel-Crafts acylation as k
Studies directed towards the total synthesis of feigrisolide B
Sharma,Kumar, K. Raman
, p. 2323 - 2326 (2007/10/03)
Attempts directed towards the total synthesis of feigrisolide B resulted in the synthesis of lactones 1 and 2. The synthesis of 1 and 2 was achieved from d-glucose and l-malic acid, respectively, with a Ti(IV) mediated diastereoselective aldol reaction as
