Catalytic asymmetric hydrogenation of quinoline carbocycles: unusual chemoselectivity in the hydrogenation of quinolines-Reference-Cited by-同舟云学术

Catalytic asymmetric hydrogenation of quinoline carbocycles: unusual chemoselectivity in the hydrogenation of quinolines

Published:2015 Issue:35 Volume:51 Page:7558-7561
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Kuwano Ryoichi¹²³⁴⁵,Ikeda Ryuhei¹²³⁴⁵,Hirasada Kazuki¹²³⁴⁵

Affiliation:

1. Department of Chemistry

2. Graduate School of Sciences, and International Research Center for Molecular Systems (IRCMS)

3. Kyushu University

4. Fukuoka 812-8581

5. Japan

Abstract

A chiral PhTRAP–ruthenium catalyst selectively hydrogenates the quinoline carbocycles to afford 5,6,7,8-tetrahydroquinolines with up to 91 : 9 er.

Funder

Japan Science and Technology Agency

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2015/CC/C5CC01971K

Reference62 articles.

1. Asymmetric hydrogenation of aromatic compounds

2. Asymmetric Hydrogenation of Heteroaromatic Compounds

3. Catalytic Asymmetric Hydrogenation of 5-Membered Heteroaromatics

4. Asymmetric Hydrogenation of Heteroarenes and Arenes

5. Enantioselective Hydrogenation of Isoquinolines

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