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.
中科院分区:
文献类型:
--
作者:
Tambar, Uttam K.;Lee, Sharon K.;Leighton, James L.
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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影响因子:
16.6
作者:
Sundén, H;Ibrahem, I;Córdova, A
通讯作者:
Córdova, A
影响因子:
15
作者:
Berger, R;Duff, K;Leighton, JL
通讯作者:
Leighton, JL
影响因子:
16.6
作者:
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通讯作者:
Akiyama, Takahiko
影响因子:
2.1
作者:
LOVEN, RP;ZUNNEBELD, WA;SPECKAMP, WN
通讯作者:
SPECKAMP, WN
影响因子:
2.6
作者:
Rowland, Gerald B.;Rowland, Emily B.;Antilla, Jon C.
通讯作者:
Antilla, Jon C.