Synthesis of C-Glycosides via Ramberg-Backlund Reaction

A novel methodology has been described, employing the Ramberg-Bäcklund rearrangement to synthesize C-glycosides. The Ramberg-Bäcklund sequence to provide C-glycosides includes three intermediates: thioglycoside, sulfonyl glycoside, and exo-glycal. Thio-glycosides can be easily made using different methods. Sulfone formation was routine with MMPP. The one-pot Ramberg-Bäcklund reaction of sulfone was done using C2Br2F4 , t-BuOH and KOH/Al2O3 under reflux to afford an exo-glycal intermediate. The belta-C-glycosides can be made by hydrogenolysis of exo-glycals using H2 and Pd/C. The alpha-C-glycosides can be made stereoselectively from exo-glycals via intramolecular ionic hydrogenation as the key step. Some of the C- glycerolipids that have been prepared exhibit strikingly similar in vitro antiproliferative effects to those of O-glycoside analogs.

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received her Ph.D.degree in Organic Chemistry(02/2002)at the City University of New York. She began her postdoctoral research at Memorial Sloan-Kettering Cancer Center (MSKCC) New York. She is working at organic synthesis core facility at MSKCC as a senior research scientist since 2008.