Divergent oriented synthesis (DOS) of aza-heterocyclic amides through palladium-catalyzed ketenimination of 2-iodo-N-(propa-1,2-dien-1-yl)anilines-Reference-Cited by-同舟云学术

Divergent oriented synthesis (DOS) of aza-heterocyclic amides through palladium-catalyzed ketenimination of 2-iodo-N-(propa-1,2-dien-1-yl)anilines

Published:2020 Issue:6 Volume:7 Page:890-895
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Chen Xiaoyan¹²³⁴⁵,Qiu Guanyinsheng⁶⁷⁸⁹¹⁰,Liu Renzhi⁶⁷⁸⁹¹⁰,Chen Dianpeng¹¹¹²¹³¹⁰^ORCID,Chen Zhiyuan¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory of Functional Small Organic Molecules

2. Ministry of Education and College of Chemistry & Chemical Engineering

3. Jiangxi Normal University

4. Nanchang

5. P. R. China

6. College of Biological

7. Chemical Sciences and Engineering

8. Jiaxing University

9. Jiaxing 314001

10. China

11. Chemistry and Chemical Engineering

12. Qufu Normal University

13. Qufu 273165

Abstract

A palladium-catalyzed tandem reaction of N-(2-iodophenyl)-4-methyl-N-(propa-1,2-dien-1-yl)benzenesulfonamide with isocyanide is described to divergently produce aza-heterocyclic amides.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/QO/C9QO01451A

Reference62 articles.

1. Still Unconquered: Enantioselective Passerini and Ugi Multicomponent Reactions

2. To each his own: isonitriles for all flavors. Functionalized isocyanides as valuable tools in organic synthesis

3. Metal-mediated post-Ugi transformations for the construction of diverse heterocyclic scaffolds

4. Metal-catalyzed C–H functionalization involving isocyanides

5. Metal-Mediated and Metal-Catalyzed Reactions of Isocyanides

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