Synthesis from d-Altrose of (5R,6R,7R,8S)-5,7-Dihydroxy-8-hydroxymethylconidine and 2,4-Dideoxy-2,4-imino-d-glucitol, Azetidine Analogues of Swainsonine and 1,4-Dideoxy-1,4-imino-d-mannitol
摘要:
Ring closure of a 3,5-di-O-triflate derived from D-altrose with benzylamine allowed the formation of both monocyclic and bicyclic azetidine analogues of swainsonine.
Synthesis from <scp>d</scp>-Altrose of (5<i>R</i>,6<i>R</i>,7<i>R</i>,8<i>S</i>)-5,7-Dihydroxy-8-hydroxymethylconidine and 2,4-Dideoxy-2,4-imino-<scp>d</scp>-glucitol, Azetidine Analogues of Swainsonine and 1,4-Dideoxy-1,4-imino-<scp>d</scp>-mannitol
作者:Noelia Araújo、Sarah F. Jenkinson、R. Fernando Martínez、Andreas F. G. Glawar、Mark R. Wormald、Terry D. Butters、Shinpei Nakagawa、Isao Adachi、Atsushi Kato、Akihide Yoshihara、Kazuya Akimitsu、Ken Izumori、George W. J. Fleet
DOI:10.1021/ol301844n
日期:2012.8.17
Ring closure of a 3,5-di-O-triflate derived from D-altrose with benzylamine allowed the formation of both monocyclic and bicyclic azetidine analogues of swainsonine.