An efficient synthesis of styrenyl enamides from 4-aryl-2-oxazolidinones in the presence of strong base-Reference-Cited by-同舟云学术

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An efficient synthesis of styrenyl enamides from 4-aryl-2-oxazolidinones in the presence of strong base

Published:2015-10 Issue:41 Volume:56 Page:5517-5520
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Zou Kaihe,Ye Jinxing,Wu Xin-Yan

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference57 articles.

1. Enamides: valuable organic substrates

2. Enamides and Enecarbamates as Nucleophiles in Stereoselective C–C and C–N Bond-Forming Reactions

3. Use of Nonfunctionalized Enamides and Enecarbamates in Asymmetric Synthesis

4. Enamides and Related Functional Groups as Nucleophilic Components in Ring-Forming Processes Catalyzed by Electrophilic Metal Salts

Cited by 3 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. Regioselective Ring‐Opening of Styrene Oxide Derivatives Using Halohydrin Dehalogenase for Synthesis of 4‐Aryloxazolidinones;Advanced Synthesis & Catalysis;2019-08-26

2. A convenient synthesis of N -vinyl enamides via the lithiation and ring-opening reaction of 2-phenyl-2-oxazolines;Tetrahedron Letters;2017-05

3. ChemInform Abstract: An Efficient Synthesis of Styrenyl Enamides from 4-Aryl-2-oxazolidinones in the Presence of Strong Base.;ChemInform;2016-01

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