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.
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.
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DOI：
10.1021/ol301844n
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发表时间：
2012-07
期刊：
影响因子：
5.2
通讯作者：
Noelia Araújo;S. F. Jenkinson;R. Martínez;Andreas F. G. Glawar;M. Wormald;T. Butters;S. Nakagawa;I. Adachi;A. Kato;A. Yoshihara;K. Akimitsu;K. Izumori;G. Fleet
中科院分区：
文献类型：
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作者：
Noelia Araújo;S. F. Jenkinson;R. Martínez;Andreas F. G. Glawar;M. Wormald;T. Butters;S. Nakagawa;I. Adachi;A. Kato;A. Yoshihara;K. Akimitsu;K. Izumori;G. Fleet
由D-阿卓糖衍生的3，5-二-O-三氟甲磺酸酯与苄胺的闭环允许形成苦马豆素的单环和双环氮杂环丁烷类似物。
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.