Economical Access to Diverse Enantiopure Tetrahydropyridines and Piperidines Enabled by Catalytic Borrowing Hydrogen-Reference-Cited by-同舟云学术

Economical Access to Diverse Enantiopure Tetrahydropyridines and Piperidines Enabled by Catalytic Borrowing Hydrogen

Published:2022-12-07 Issue:2 Volume:62 Page:
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew Chem Int Ed

Author:

Ng Teng Wei¹,Tao Ran¹²,See Willy Wei Li¹,Poh Si Bei¹,Zhao Yu¹^ORCID

Affiliation:

1. Department of Chemistry National University of Singapore 4 Science Drive 2 Singapore 117544 Republic of Singapore

2. Integrative Sciences and Engineering Programme NUS Graduate School National University of Singapore 21 Lower Kent Ridge Road Singapore 119077 Singapore

Funder

Ministry of Education - Singapore

National University of Singapore

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202212528

Reference92 articles.

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

2. For selected recent reviews see:

3. Recent developments in multicomponent synthesis of structurally diversified tetrahydropyridines

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

5. Stereospecific route to enantiopure all cis-2,3,6-trisubstituted piperidines. Facile synthesis of (−)-deoxocassine and (+)-azimic acid

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