Tandem synthesis of tetrahydroquinolines and identification of the reaction network by operando NMR-Reference-Cited by-同舟云学术

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Tandem synthesis of tetrahydroquinolines and identification of the reaction network by operando NMR

Published:2021 Issue:13 Volume:11 Page:4332-4341
ISSN:2044-4753
Container-title:Catalysis Science & Technology
language:en
Short-container-title:Catal. Sci. Technol.

Author:

Chen Jingwen¹²³⁴⁵^ORCID,Qi Long⁶⁷⁸⁹^ORCID,Zhang Biying¹⁰⁷⁸⁹,Chen Minda¹⁰⁷⁸⁹^ORCID,Kobayashi Takeshi⁶⁷⁸⁹^ORCID,Bao Zongbi¹²³⁴⁵,Yang Qiwei¹²³⁴⁵,Ren Qilong¹²³⁴⁵,Huang Wenyu¹⁰⁷⁸⁹^ORCID,Zhang Zhiguo¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory of Biomass Chemical Engineering of Ministry of Education

2. College of Chemical and Biological Engineering

3. Zhejiang University

4. Hangzhou 310027

5. China

6. U.S. DOE Ames Laboratory

7. Iowa State University

8. Iowa 50011

9. USA

10. Department of Chemistry

Abstract

Bifunctional MOF supported Pd nanoparticles for the one-pot tandem synthesis of substituted tetrahydroquinolines were developed, and operando high-pressure MAS-NMR were performed to understand the complex reaction network.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

China Postdoctoral Science Foundation

U.S. Department of Energy

National Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2021/CY/D1CY00418B

Reference69 articles.

1. Recent progress in the synthesis of 1,2,3,4,-tetrahydroquinolines

2. Hydrogen storage in liquid organic heterocycles

3. Advances in the Chemistry of Tetrahydroquinolines

4. Expanding the tetrahydroquinoline pharmacophore

5. A structural study of 1-phenyl-1,2,3,4-tetrahydroquinoline-based dyes for solid-state DSSC applications

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