Rapid Synthesis of α-Chiral Piperidines via a Highly Diastereoselective Continuous Flow Protocol-Reference-Cited by-同舟云学术

Rapid Synthesis of α-Chiral Piperidines via a Highly Diastereoselective Continuous Flow Protocol

Published:2022-04-22 Issue:17 Volume:24 Page:3205-3210
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Shan Chao¹,Xu Jinping¹,Cao Liming¹,Liang Chaoming²,Cheng Ruihua²,Yao Xiantong²,Sun Maolin²,Ye Jinxing¹²^ORCID

Affiliation:

1. Engineering Research Center of Pharmaceutical Process Chemistry, Ministry of Education, School of Pharmacy, East China University of Science and Technology, Shanghai 200237, China

2. School of Biomedical and Pharmaceutical Sciences, Guangdong University of Technology, Guangzhou 510006, 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.2c00975

Reference42 articles.

1. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals

2. Enantioselective Oxidative Gold Catalysis Enabled by a Designed Chiral P,N-Bidentate Ligand

3. Stereoselective synthesis of 2,6-disubstituted piperidine alkaloids

4. The killer of Socrates: Coniine and Related Alkaloids in the Plant Kingdom

5. Total Synthesis of (−)-Canadine, (−)-Rotundine, (−)-Sinactine, and (−)-Xylopinine Using a Last-Step Enantioselective Ir-Catalyzed Hydrogenation

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