Synthesis of azasugars through a proline-catalyzed reaction

Synthesis of azasugars through a proline-catalyzed reaction
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DOI:
10.1021/jo060568b
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发表时间:
2006-08-04
影响因子:
3.6
通讯作者:
Fernandez-Mayoralas, Alfonso
Fernandez-Mayoralas, Alfonso
中科院分区:
化学2区
文献类型:
--
作者:
Calderon, Felix;Doyaguez, Elisa G.;Fernandez-Mayoralas, Alfonso

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我们报告了一种从对映体纯的 L-和 D-酒石酸二乙酯中获得氮杂糖的有效途径。关键步骤是脯氨酸催化的羟醛缩合,其中脯氨酸的两种对映体都被用作催化剂,提供互补的反羟醛产物。
We report an efficient route to obtain azasugars from the enantiomerically pure L- and D-diethyltartrate. The key step is a proline-catalyzed aldol condensation, in which both enantiomers of proline have been used as catalyst, affording complementary anti-aldol products.