Synthesis of reverse glycosyl fluorides <i>via</i> organophotocatalytic decarboxylative fluorination of uronic acids-Reference-Cited by-同舟云学术

Synthesis of reverse glycosyl fluorides via organophotocatalytic decarboxylative fluorination of uronic acids

Published:2022 Issue:10 Volume:9 Page:2808-2814
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Ding Han¹^ORCID,Yan Ningjie¹,Wang Peng¹,Song Ni¹,Sun Qikai¹,Li Tiantian¹,Li Ming¹²^ORCID

Affiliation:

1. Key Laboratory of Marine Medicine, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, P. R. China

2. Laboratory for Marine Drugs and Bioproducts, Pilot National Laboratory for Marine Science and Technology, Qingdao 266237, P. R. China

Abstract

Mes-Acr*-catalyzed decarboxylative fluorination of structurally diverse uronic acids under blue light irradiation provides an alternative avenue for the synthesis of reverse glycosyl fluorides of medicinal and biological relevance.

Funder

National Natural Science Foundation of China-Shandong Joint Fund

Natural Science Foundation of Shandong Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO00133K

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1. Biosynthesis of the Fluorinated Natural Product Nucleocidin inStreptomyces calvusIs Dependent on thebldA-Specified Leu-tRNAUUAMolecule