Mechanism and stereospecificity of Z-enamide synthesis from salicylaldehydes with isoxazoles using DFT calculations-Reference-Cited by-同舟云学术

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Mechanism and stereospecificity of Z-enamide synthesis from salicylaldehydes with isoxazoles using DFT calculations

Published:2019-12 Issue: Volume:903 Page:120981
ISSN:0022-328X
Container-title:Journal of Organometallic Chemistry
language:en
Short-container-title:Journal of Organometallic Chemistry

Author:

Ling Baoping^ORCID,Jiang Yuan-Ye^ORCID,Liu Yuxia^ORCID,Liu Peng,Liu Rutao,Bi Siwei^ORCID

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

High Performance Computing Center of Qufu Normal University

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference88 articles.

1. (For selected examples of enamides):

2. Steroselective synthesis of alkyl-, aryl-, vinyl- and alkynyl-substituted Z-enamides and enol ethers;Caramenti;Chem. Sci.,2019

3. Tertiary enamide-triggered SEAr: domino allylation and enamine-type addition;Beltran;Org. Lett.,2019

4. Tertiary enamides: versatile and available substrates in synthetic chemistry;Cai;Curr. Org. Synth.,2019

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