Retini, Michele; Bartolucci, Silvia; Bartoccini, Francesca; Mari, Michele; Piersanti, Giovanni published the artcile< Concise and Convergent Enantioselective Total Syntheses of (+)- and (-)-Fumimycin>, Related Products of 112-63-0, the main research area is fumimycin enantioselective synthesis.
The concise and convergent total syntheses of (+)- and (-)-Fumimycin (I) have been achieved by taking advantage of strategies for the asym. aza-Friedel-Crafts reaction of a highly substituted hydroquinone and N-fumaryl ketimine generated from the corresponding dehydroalanine. The enantiomerically pure natural product and its enantiomer were prepared in seven steps and 22% overall yield by employing both enantiomers of a BINOL-derived chiral phosphoric acid (CPA) catalyst.
Journal of Organic Chemistry published new progress about Enantioselective synthesis. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Related Products of 112-63-0.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics