NiCl2(PPh3)2–Zn Promoted Deallyloxycarbonylative Directed Aldo Reaction of Allyl β-Keto Carboxylates with Aldehydes to β-Hydroxy Ketones
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/20/11/20_11_2023/_pdf
Reference2 articles.
1. The palladium-catalyzed directed aldol reaction of aldehydes with ketone enolates generated by the decarboxylation of allyl .beta.-keto carboxylates under neutral conditions
Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. 2.10 The Aldol Reaction: Transition Metal Enolate;Comprehensive Organic Synthesis II;2014
2. Stereoselective Direct Amine-Catalyzed Decarboxylative Aldol Addition;Organic Letters;2011-03-07
3. ChemInform Abstract: NiCl2(PPh3)2-Zn-Promoted Deallyloxycarbonylative Directed Aldol Reaction of Allyl β-Keto Carboxylates (I) with Aldehydes (II) to β-Hydroxy Ketones (III).;ChemInform;2010-08-21
4. Preparation of Alcohols;Compendium of Organic Synthetic Methods;2006-11-22
5. Transition Metal Catalyzed Decarboxylative Additions of Enolates;European Journal of Organic Chemistry;2005-04-25
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