Pericyclic cascade with chirality transfer: reaction pathway and origin of enantioselectivity of the hetero-Claisen approach to oxindoles.
Pericyclic cascade with chirality transfer: reaction pathway and origin of enantioselectivity of the hetero-Claisen approach to oxindoles.
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DOI:
10.1002/anie.201105412
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发表时间:
2011-11-25
影响因子:
16.6
通讯作者:
Houk, Kendall N.
中科院分区:
文献类型:
--
作者:
Celebi-Oelcuem, Nihan;Lam, Yu-hong;Richmond, Edward;Ling, Kenneth B.;Smith, Andrew D.;Houk, Kendall N.
Cascade reactions [1] are of increasing value in organic synthesis due to their potential for expedient generation of molecular complexity. Pericyclic cascades [1, 2] are especially appealing by virtue of their often predictable and exquisite stereochemical control. The diverse pericyclic cascades devised for target-oriented syntheses often act on substrates bearing well-recognized structural motifs with amply documented reactivity requirements and stereochemical properties. Nevertheless, the interplay between theory and experiment continues to uncover novel cascade mechanisms with new or underexplored reactivity patterns. Indeed, for the 2+ 2 cycloadditions of ketenes with 1, 3-dienes [3] and imines,[4] the
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影响因子:
3.6
作者:
ABOUGHARBIA, MA;JOULLIE, MM
通讯作者:
JOULLIE, MM
影响因子:
5.2
作者:
Akerling, ZR;Norton, JE;Houk, KN
通讯作者:
Houk, KN
影响因子:
5.2
作者:
Hayden, Amy E.;Xu, Hao;Houk, K. N.
通讯作者:
Houk, K. N.
影响因子:
15
作者:
Cannizzaro, CE;Houk, KN
通讯作者:
Houk, KN
DOI:
10.1039/p19850001837
发表时间:
1985-01-01
期刊:
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
影响因子:
--
作者:
FALSHAW, CP;HASHI, NA;TAYLOR, GA
通讯作者:
TAYLOR, GA