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亚胺与氮杂锆环丁烯的反应及缺电子亚胺锆茂配合物的生成

Reactions of Imines with Azazirconacyclobutenes and Generation of Electron-Deficient Imidozirconocene Complexes.

作者信息

Ruck Rebecca T, Bergman Robert G

机构信息

Department of Chemistry and Center for New Directions in Organic Synthesis, University of California, Berkeley, Berkeley, California 94720.

出版信息

Organometallics. 2004 May 10;23(10):2231-2233. doi: 10.1021/om0497994.

DOI:10.1021/om0497994
PMID:16508694
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1383655/
Abstract

Electron-deficient imines are shown to insert into the zirconium-carbon bond of azazirconacyclobutenes to generate new six-membered ring metallacycles. On heating, these expanded zirconacycles undergo a retro-[4 + 2] cycloaddition to generate alpha,beta-unsaturated imines in excellent yields and novel, fully characterized electron-deficient imidozirconocene complexes.

摘要

缺电子亚胺可插入氮杂锆环丁烯的锆-碳键中,生成新的六元环金属环化物。加热时,这些扩环锆环化物会发生逆-[4 + 2]环加成反应,以优异的产率生成α,β-不饱和亚胺以及新型的、经充分表征的缺电子亚胺基锆茂配合物。

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本文引用的文献

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Reactivity of Zirconocene Azametallacyclobutenes: Insertion of Aldehydes, Carbon Monoxide, and Formation of alpha,beta-Unsaturated Imines. Formation and Trapping of [Cp(2)Zr=O] in a [4 + 2] Retrocycloaddition(1).锆茂氮杂金属环丁烯的反应活性:醛、一氧化碳的插入反应以及α,β-不饱和亚胺的形成。在[4 + 2]逆环加成反应中[Cp₂Zr=O]的形成与捕获(1)
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The First Catalytic Asymmetric Nitro-Mannich-Type Reaction Promoted by a New Heterobimetallic Complex.一种新型异双金属配合物促进的首例催化不对称硝基-曼尼希型反应。
Angew Chem Int Ed Engl. 1999 Dec 3;38(23):3504-3506. doi: 10.1002/(sici)1521-3773(19991203)38:23<3504::aid-anie3504>3.0.co;2-e.
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