纸质出版:1985
移动端阅览
[1]曹玲华 ,刘育亭.N苷Amadori重排的研究(Ⅰ)[J].新疆大学学报(自然科学版),1985(03):77-80.
曹玲华, 刘育亭. N苷Amadori重排的研究(Ⅰ)[J]. Journal of Xinjiang University (Natural Science Edition in Chinese and English), 1985, (3).
由Amadori在1926—1931年间发表的研究成果而得名的Amadori重排反应
迄今为止仍为人们所重视
是由于这个反应十分巧妙
应用甚广。在温和的条件下
还原糖与含有氨基的化合物反应
生成N苷糖基胺
由于酸的催化重排成相应的N苷酮糖
这就是Amadori重排反应
例如
D—葡萄糖和苯胺作用可得到
Reducing Sugars react readily
under mild conditions
with compounds containingthe primary amine group
this reaction was named the Amadori rearrangement.1-Deoxy-1-P-toluidino-D-fructose
1-Deoxy-1-P-toluidino-D-mannose
1-Deoxy-1-P-toluidino-galactose
1-Deoxy-1-P-toluidino-rhamnose
1-Deoxy-1-P-toluidino-Sorbose
1-Deoxy-1-P-toluidino-xylose
1-Deoxy-1-P-toluidino-arabinose' 1-Deoxy-1-P-toluidino-lactose
1-Deoxy-1-P-toluidino-maltose have been obtained by Ama-dori rearrangement. The beautiful crystalline of the acetate derivatives have beenobtained. These are: N-P-toluidino-D-mannopyrano Sylamine-2
3
4
6-tetraacetate
N-P-toluidino-D-xylofuranosylamine-2
3
5-triacetate
N-P-toluidino-L-rhamnopy-ranosylamine-2
3
4-triacetate
N-P-toluidino-lactosylamine-heptaacetate
N-P-toluidinomaltosylamine-haptaacetate.
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