Enantioselective Reduction of 3-Substituted Quinolines with a Cyclopentadiene-Based Chiral Brønsted Acid-Reference-Cited by-同舟云学术

Enantioselective Reduction of 3-Substituted Quinolines with a Cyclopentadiene-Based Chiral Brønsted Acid

Published:2017-05-08 Issue:14 Volume:49 Page:3157-3164
ISSN:0039-7881
Container-title:Synthesis
language:en
Short-container-title:Synthesis

Author:

Tang Weijun¹^ORCID,Zhao Xiaofang¹,Xiao Jianliang¹²

Affiliation:

1. Key Laboratory of Applied Surface and Colloid Chemistry of Ministry of Education, and School of Chemistry & Chemical Engineering, Shaanxi Normal University

2. Department of Chemistry, University of Liverpool

Abstract

Enantioselective reduction of 3-substituted quinolines has been achieved using a cyclopentadiene-based chiral Brønsted acid as catalyst and Hantzsch ester as hydrogen donor, affording the corresponding tetrahydroquinolines in good enantioselectivities.

Funder

National Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0036-1589012.pdf

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