Enantioselective (formal) aza-Diels-Alder reactions with non-Danishefsky-type dienes.

Enantioselective (formal) aza-Diels-Alder reactions with non-Danishefsky-type dienes.
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与非丹尼舍夫斯基型二烯的对映选择性(形式)氮杂-狄尔斯-阿尔德反应。

DOI:
10.1021/ja104480g
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发表时间:
2010-08-04
影响因子:
15
通讯作者:
Leighton, James L.
Leighton, James L.
中科院分区:
化学1区
文献类型:
--
作者:
Tambar, Uttam K.;Lee, Sharon K.;Leighton, James L.

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Enantioselective (formal) aza-Diels-Alder reactions between acylhydrazones and non-Danishefsky-type dienes have been developed. The reactions are promoted by a simple and economical chiral silicon Lewis acid, and are typically conducted at ambient temperature. Both glyoxylate and aliphatic aldehyde-derived hydrazones may be employed, as may variously substituted dienes, leading to the synthesis of a diverse array of tetrahydropyridines with good to excellent levels of enantioselectivity.
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