Gold-Catalyzed Addition of β-Ketoesters to Alkenes: Influence of Electronic and Steric Effects in the Reaction Outcome

被引:0
|
作者
La-Venia, Agustina [1 ]
Mischne, Mirta P. [1 ]
Mata, Ernesto G. [1 ]
机构
[1] Univ Nacl Rosario, CONICET, Inst Quim Rosario, Fac Ciencias Bioquim & Farmaceut, Suipacha 531,Rosario S2002LRK, Rosario, Santa Fe, Argentina
来源
MOLECULES | 2018年 / 23卷 / 03期
关键词
gold catalysis; hydroalkylation; beta-ketoesters; olefins; UNACTIVATED ALKENES; C-C; INTRAMOLECULAR ADDITION; MULTIPLE BONDS; HYDROAMINATION; ACTIVATION; SILVER; HYDROALKYLATION; POLYMERIZATION; HETEROCYCLES;
D O I
10.3390/molecules23030629
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The gold-catalyzed intermolecular hydroalkylation of olefins with beta-ketoesters represents a conceptually attractive and useful synthetic tool; however, it has been scarcely applied, remaining a challenge for chemists. The aim of the current study was to investigate the addition of these 1,3-diketo-compounds to alkenes under gold catalysis conditions, in order to establish the electronic and steric effects of the alkenyl substrates in the reaction outcome. The screening of different catalyst systems and diverse olefins enabled defining the alkenyl requirements and the best reaction conditions to efficiently achieve the coupled products.
引用
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页数:11
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