Stereoselective Access to Highly Substituted Vinyl Ethers via trans-Difunctionalization of Alkynes with Alcohols and Iodine(III) Electrophile-Reference-Cited by-同舟云学术

Stereoselective Access to Highly Substituted Vinyl Ethers via trans-Difunctionalization of Alkynes with Alcohols and Iodine(III) Electrophile

Published:2020-05-04 Issue:19 Volume:142 Page:8619-8624
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Ding Wei¹,Chai Jinkui¹²,Wang Chen¹³^ORCID,Wu Junliang²,Yoshikai Naohiko¹^ORCID

Affiliation:

1. Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore

2. College of Chemistry, Henan Institute of Advanced Technology, Zhengzhou University, Zhengzhou 450001, P. R. China

3. Zhejiang Key Laboratory of Alternative Technologies for Fine Chemical Process, Shaoxing University, Shaoxing 312000, P. R. China

Funder

Ministry of Education - Singapore

Nanyang Technological University

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.0c04140

Reference51 articles.

1. Cyclisation Reactions Involving Alkyl Enol Ethers

2. Platinum(II)-Catalyzed Generation and [3+2] Cycloaddition Reaction of α,β-Unsaturated Carbene Complex Intermediates for the Preparation of Polycyclic Compounds

3. Enantioselective Gold(I)-Catalyzed Vinylogous [3 + 2] Cycloaddition between Vinyldiazoacetates and Enol Ethers

4. Diarylrhodates as Promising Active Catalysts for the Arylation of Vinyl Ethers with Grignard Reagents

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