Synthesis of (?) cephalosporolide E and (+) cephalosporolide F utilizing the vinylogous Mukaiyama type reaction with an α-chloro sulfide?

RSC Advances Pub Date: 2016-07-27 DOI: 10.1039/C6RA13861F

Abstract

The synthesis of cephalosporolide E and F is described utilizing diastereoselective reduction of a propargylic ketone using a Noyori catalyst to create the C6 carbinol stereogenic center. A vinylogous silylketene acetal addition to an α-chloro sulfide is exploited for stereoselective carbon–carbon bond formation and introduction of the butenolide moiety. Oxidative radical cyclization is utilized for the creation of the [5,5]-spiroketal moiety.

Graphical abstract: Synthesis of (?) cephalosporolide E and (+) cephalosporolide F utilizing the vinylogous Mukaiyama type reaction with an α-chloro sulfide
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