Enantioselective H-bond-directed vinylogous iminium ion strategy for the functionalization of vinyl-substituted heteroaryl aldehydes-Reference-Cited by-同舟云学术

Enantioselective H-bond-directed vinylogous iminium ion strategy for the functionalization of vinyl-substituted heteroaryl aldehydes

Published:2021 Issue:13 Volume:57 Page:1667-1670
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Skrzyńska Anna¹²³⁴⁵,Frankowski Sebastian¹²³⁴⁵,Topolska Aleksandra¹²³⁴⁵,Dyguda Mateusz¹²³⁴⁵,Gao Xin-Yue⁶⁷⁸⁹¹⁰,Xu Chang-Jiang⁶⁷⁸⁹¹⁰,Chen Ying-Chun⁶⁷⁸⁹¹⁰^ORCID,Albrecht Łukasz¹²³⁴⁵^ORCID

Affiliation:

1. Institute of Organic Chemistry

2. Faculty of Chemistry

3. Lodz University of Technology

4. Żeromskiego 116

5. 90-924 Łódź

6. Key Laboratory of Drug-Targeting and Drug Delivery System of the Ministry of Education and Sichuan Research Center for Drug Precision Industrial Technology

7. West China School of Pharmacy

8. Sichuan University

9. Chengdu 610041

10. China

Abstract

The first H-bond directed functionalization of of vinyl-substituted heteroaromatic aldehydes via the H-bond-directed vinylogous iminium ion based strategy has been described.

Funder

Narodowe Centrum Nauki

National Natural Science Foundation of China

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/2021/CC/D0CC07765H

Reference52 articles.

1. The ying and yang of asymmetric aminocatalysis

2. Iminium Catalysis

3. Asymmetric Enamine Catalysis

4. Asymmetric Aminocatalysis-Gold Rush in Organic Chemistry

5. Recent advances in asymmetric catalysis with cinchona alkaloid-based primary amines

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