Carbocyclization of Carbohydrates: Diastereoselective Synthesis of (+)-Gabosine F, (−)-Gabosine O, and (+)-4-<i>epi</i>-Gabosine O
作者:Tony K. M. Shing、King H. So、Wun S. Kwok
DOI:10.1021/ol902071e
日期:2009.11.5
Exploitation of silica gel/chloramine T mediated intramolecular nitrile oxide-alkene cycloaddition (INOC) of sugar-derived oximes to carbocycles furnished the first synthesis of gabosine F from L-arabinose in 12 steps with 23% overall yield, thereby confirming it absolute configuration. Similarly, efficient syntheses of gabosine O and 4-epi-gabosine O were accomplished from D-Mannose in 9 and 11 steps with 41% and 38% overall yields, respectively, involving INOC, regioselective dehydration, and diastereciselective hydrogenation as the key steps.