DFT study on the mechanism of bimetallic Pd–Zn-catalyzed cycloaddition of alkynyl aryl ethers with internal alkynes-Reference-Cited by-同舟云学术

DFT study on the mechanism of bimetallic Pd–Zn-catalyzed cycloaddition of alkynyl aryl ethers with internal alkynes

Published:2020 Issue:9 Volume:49 Page:2914-2923
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Wang Mei-yan¹²³⁴⁵,Chen Li⁶⁷³⁸⁵,Li Bing-wen¹²³⁴⁵,Liu Jing-yao¹²³⁴⁵^ORCID

Affiliation:

1. Laboratory of Theoretical and Computational Chemistry

2. Institute of Theoretical Chemistry

3. Jilin University

4. Changchun 130023

5. People's Republic of China

6. Department of Oral Radiology

7. School and Hospital of Stomatology

8. Changchun 130021

Abstract

C₆H₅OCCSiⁱPr₃ is the most reactive substrate, due to strong electron-withdrawing inductive effect of the O atom and relatively large steric repulsion of the SiⁱPr₃ group.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/DT/C9DT04362D

Reference33 articles.

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4. C–H Activation , ed. J.-Q. Yu and Z. Shi , Springer , Berlin , 2010

5. Transition metal-catalyzed C–H bond functionalizations by the use of diverse directing groups

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