Furan-2-yl Anions as γ-Oxo/Hydroxyl Acyl Anion Equivalents Enabled by Iridium-Catalyzed Chemoselective Reduction-Reference-Cited by-同舟云学术

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Furan-2-yl Anions as γ-Oxo/Hydroxyl Acyl Anion Equivalents Enabled by Iridium-Catalyzed Chemoselective Reduction

Published:2023-06-20 Issue:25 Volume:25 Page:4705-4710
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Tingting¹,Miao Rui²,Luo Renshi²³^ORCID,Xu Jiaxi¹^ORCID,Yang Zhanhui¹^ORCID

Affiliation:

1. Department of Organic Chemistry, College of Chemistry, Beijing University of Chemical Technology, Beijing 100029, People’s Republic of China

2. School of Pharmaceutical Sciences, Gannan Medical University, Ganzhou, Jiangxi 341000, People’s Republic of China

3. College of Chemistry and Environmental Engineering, Shaoguan University, Shaoguan, Guangdong 512005, People’s Republic of China

Funder

Beijing Municipal Natural Science Foundation

Fundamental Research Funds for the Central Universities

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c01634

Reference46 articles.

1. New horizons in carbonyl chemistry: reagents for nucleophilic acylation

2. The Benzoin and Related Acyl Anion Equivalent Reactions

3. Reactions of acyl anion equivalents derived from cyanohydrins, protected cyanohydrins and α-dialkylaminonitriles

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