Access to 1-amino-3,4-dihydroisoquinolines via palladium-catalyzed C–H bond aminoimidoylation reaction from functionalized isocyanides-Reference-Cited by-同舟云学术

Access to 1-amino-3,4-dihydroisoquinolines via palladium-catalyzed C–H bond aminoimidoylation reaction from functionalized isocyanides

Published:2019 Issue:72 Volume:9 Page:42072-42076
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Xiong Zhuang¹²³⁴,Cai Panyuan⁵⁶⁷⁸⁹,Mei Yingshuang¹²³⁴,Wang Jian⁵⁶⁷⁸⁹^ORCID

Affiliation:

1. School of Biotechnology and Sciences

2. Wuyi University

3. Jiangmen

4. P. R. China

5. Key Laboratory of Functional Molecular Solids

6. Ministry of Education

7. Anhui Laboratory of Molecule-Based Materials

8. College of Chemistry and Materials Science

9. Anhui Normal University

Abstract

Efficient and practice access to 1-amino-3,4-dihydroisoquinolines, through palladium-catalyzed intramolecular C–H bond aminoimidoylation of α-benzyl-α-isocyanoacetates, has been developed.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Anhui Province

Anhui Normal University

Wuyi University

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/RA/C9RA09139D

Reference59 articles.

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4. Metal-free sulfonyl radical-initiated cascade cyclization to access sulfonated indolo[1,2-a]quinolines

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