Catalytic Enantioselective Construction of Chiral γ-Azido Nitriles through Nitrile Group-Promoted Electrophilic Reaction of Alkenes-Reference-Cited by-同舟云学术

Catalytic Enantioselective Construction of Chiral γ-Azido Nitriles through Nitrile Group-Promoted Electrophilic Reaction of Alkenes

Published:2023-09-01 Issue:36 Volume:25 Page:6757-6762
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Liang Yaoyu¹,Huang Hongtai¹,Huang Nan¹,Liao Lihao¹,Zhao Xiaodan¹^ORCID

Affiliation:

1. Institute of Organic Chemistry & MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-Sen University, Guangzhou, Guangdong 510006, P. R. China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c02650

Reference49 articles.

1. Bioconjugation via azide–Staudinger ligation: an overview

2. Click Chemistry for Drug Development and Diverse Chemical–Biology Applications

3. Nitrile-Containing Pharmaceuticals: Efficacious Roles of the Nitrile Pharmacophore

4. A survey of the role of nitrile groups in protein–ligand interactions

5. A new, versatile and stereospecific route to unusual amino acids: the enantiospecific total synthesis of statine amide and its three stereoisomers

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1. Catalytic Enantioselective Electrophilic Difunctionalization of Unsaturated Sulfones;Organic Letters;2024-05-17

2. Catalytic Enantioselective Aminative Difunctionalization of Alkenes;Journal of the American Chemical Society;2024-03-01