Addition reactions of O-bound cyclic nickel enolates to α,β-unsaturated ketones

被引:14
作者
Cámpora, J
Maya, CM
Palma, P
Carmona, E
Graiff, C
Tiripicchio, A
机构
[1] Univ Seville, CSIC, Inst Invest Quim, Seville 41092, Spain
[2] Univ Parma, Dipartimento Chim Gen & Inorgan, I-43100 Parma, Italy
关键词
D O I
10.1039/b303062h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The addition of the O-bound nickel enolates Ni(C6H4-o-C(NCHR)O)(dippe) (R = H, 1; R = Me, 2) to alpha,beta-unsaturated ketones proceeds with complete stereoselectivity giving rise to [ 2 + 4] cycloadducts that can further evolve to generate open-chain, Michael-like products. The stereoselectivity of these reactions suggests a concerted mechanism, through an exo transition state.
引用
收藏
页码:1742 / 1743
页数:2
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