Palladium(<scp>ii</scp>)-catalyzed 1,3-heteroaryl acyloxylation of propargylic electrophiles-Reference-Cited by-同舟云学术

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Palladium(ii)-catalyzed 1,3-heteroaryl acyloxylation of propargylic electrophiles

Published:2024 Issue:15 Volume:11 Page:4077-4083
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Teng Shenghan¹^ORCID,Liang Peiyao¹,Hu Lin¹,Chen Siyi¹,Wang Shoulei¹^ORCID,Huang Wei¹²

Affiliation:

1. Strait Laboratory of Flexible Electronics (SLoFE), Strait Institute of Flexible Electronics (SIFE, Future Technologies), Fujian Normal University, Fuzhou, 350117, China

2. Frontiers Science Center for Flexible Electronics (FSCFE), MIIT Key Laboratory of Flexible Electronics (KLoFE), Northwestern Poly-technical University, Xi'an, 710072, China

Abstract

Here, we report a regio- and stereo-defined 1,3-heteroaryl acyloxylation of 3-substituted propargylic esters with readily available heteroarenes including indoles, pyrroles, furans and thiophenes under palladium catalysis.

Funder

Fujian Normal University

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D4QO00869C

Reference63 articles.

1. Recent Progress in the Addition Reaction of Electron-Rich Alkynes and Carboxylic Acids

2. Highly Stereoselective Synthesis and Hydrogenation of (Z)-1-Alkyl-2-arylvinyl Acetates: a Wide Scope Procedure for the Preparation of Chiral Homobenzylic Esters

3. Rh-Catalyzed Asymmetric Hydrogenation of β-Branched Enol Esters for the Synthesis of β-Chiral Primary Alcohols

4. Enantioselective Aldol Reactions Catalyzed by Tin Methoxide and BINAP·Silver(I) Complex

5. Enol Esters: Versatile Substrates for Mannich-Type Multicomponent Reactions

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