Highly efficient esterification of carboxylic acids with O–H nucleophiles through acid/iodide cooperative catalysis-Reference-Cited by-同舟云学术

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Highly efficient esterification of carboxylic acids with O–H nucleophiles through acid/iodide cooperative catalysis

Published:2024 Issue:30 Volume:22 Page:6181-6188
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Zuo Dongxu¹,Xiao Xiong¹,Ma Xinyue¹,Nie Peng²,Liu Long¹^ORCID,Chen Tieqiao¹^ORCID

Affiliation:

1. Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Hainan Provincial Key Lab of Fine Chem, Hainan Provincial Fine Chemical Engineering Research Center, Hainan University, Haikou, 570228, China

2. Guizhou Institute for Food and Drug Control, 84 Shibei Road, Yunyan District, Guiyang City, Guizhou Province, 550000, China

Abstract

A highly efficient esterification of carboxylic acids with a wide range of equivalent O–H nucleophiles is achieved using acid/iodide cooperative catalysis.

Funder

National Natural Science Foundation of China

Key Research and Development Project of Hainan Province

Guizhou Science and Technology Department

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00910J

Reference77 articles.

1. Total Synthesis of Natural 8- and 9-Membered Lactones: Recent Advancements in Medium-Sized Ring Formation

2. Update 1 of: Macrolactonizations in the Total Synthesis of Natural Products

3. Elucidation of DnaE as the Antibacterial Target of the Natural Product, Nargenicin

4. A platform for the discovery of new macrolide antibiotics

5. Effect of Anabolic Androgens on Tissue Replacement in the Ear of the Rabbit

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