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Published:1985
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[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).
[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. DOI:
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). DOI:
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
5-triacetate
N-P-toluidino-L-rhamnopy-ranosylamine-2
4-triacetate
N-P-toluidino-lactosylamine-heptaacetate
N-P-toluidinomaltosylamine-haptaacetate.
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