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本文引用的文献

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Organozinc Chemistry Enabled by Micellar Catalysis. Palladium-Catalyzed Cross-Couplings between Alkyl and Aryl in Water at Room Temperature.胶束催化实现的有机锌化学。室温下水中钯催化的烷基与芳基交叉偶联反应。
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Enantioselective conjugate addition of alkylboranes catalyzed by a copper-N-heterocyclic carbene complex.铜-N-杂环卡宾配合物催化的烷基硼试剂的对映选择性共轭加成反应。
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Copper-catalyzed enantioselective allylic substitution with readily accessible carbonyl- and acetal-containing vinylboron reagents.铜催化的对映选择性烯丙基取代反应,使用易于获得的含羰基和缩醛的乙烯基硼试剂。
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Copper-catalyzed asymmetric conjugate addition to challenging Michael acceptors and synthesis of relevant target molecules.铜催化对具有挑战性的迈克尔受体的不对称共轭加成及相关目标分子的合成。
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"Silver effect" in gold(I) catalysis: an overlooked important factor.金(I)催化中的“银效应”:一个被忽视的重要因素。
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Copper-catalyzed asymmetric 1,4-addition of alkenyl alanes to N-substituted-2-3-dehydro-4-piperidones.铜催化的烯基丙二腈对 N-取代-2-3-去氢-4-哌啶酮的不对称 1,4-加成反应。
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The role of silver additives in gold-mediated C-H functionalisation.银添加剂在金介导的 C-H 官能化中的作用。
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Manipulating micellar environments for enhancing transition metal-catalyzed cross-couplings in water at room temperature.在室温的水中,通过控制胶束环境来增强过渡金属催化的交叉偶联反应。
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Highly enantioselective and regioselective copper-catalyzed 1,4 addition of grignard reagents to cyclic enynones.高对映选择性和区域选择性铜催化格氏试剂对环状烯炔酮的 1,4 加成。
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在室温下的水中,通过铜催化的共轭加成反应形成 C-C 键到烯酮上。

C-C bond formation via copper-catalyzed conjugate addition reactions to enones in water at room temperature.

机构信息

Department of Chemistry & Biochemistry, University of California, Santa Barbara, California 93106, United States.

出版信息

J Am Chem Soc. 2012 Dec 12;134(49):19985-8. doi: 10.1021/ja309409e. Epub 2012 Nov 28.

DOI:10.1021/ja309409e
PMID:23190029
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3959802/
Abstract

Conjugate addition reactions to enones can now be done in water at room temperature with in situ generated organocopper reagents. Mixing an enone, zinc powder, TMEDA, and an alkyl halide in a micellar environemnt containing catalytic amounts of Cu(I), Ag(I), and Au(III) leads to 1,4-adducts in good isolated yields: no organometallic precursor need be formed.

摘要

烯酮的共轭加成反应现在可以在室温下的水中进行,使用原位生成的有机铜试剂。将烯酮、锌粉、TMEDA 和卤代烷混合在含有催化量的 Cu(I)、Ag(I) 和 Au(III)的胶束环境中,可得到良好收率的 1,4-加成产物:无需形成有机金属前体。