Synthesis of indoles and quinazolines via additive-controlled selective C–H activation/annulation of N-arylamidines and sulfoxonium ylides-Reference-Cited by-同舟云学术

Synthesis of indoles and quinazolines via additive-controlled selective C–H activation/annulation of N-arylamidines and sulfoxonium ylides

Published:2019 Issue:28 Volume:55 Page:4039-4042
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Lai Ruizhi¹²³⁴⁵,Wu Xiaohua¹²³⁴⁵,Lv Songyang¹²³⁴⁵,Zhang Chen¹²³⁴⁵,He Maoyao¹²³⁴⁵,Chen Yuncan¹²³⁴⁵,Wang Qiantao¹²³⁴⁵,Hai Li¹²³⁴⁵^ORCID,Wu Yong¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory of Drug-Targeting of Education Ministry and Department of Medicinal Chemistry

2. West China School of Pharmacy

3. Sichuan University

4. Chengdu 610041

5. China

Abstract

Selective synthesis of indoles and quinazolines was achieved through a precise control of C–H activation/annulation by changing additives.

Funder

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/2019/CC/C9CC01146C

Reference46 articles.

1. Rhodium-Catalyzed C−C Bond Formation via Heteroatom-Directed C−H Bond Activation

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4. CH Bond Activation by f‐Block Complexes

5. Transition metal-catalysed couplings between arenes and strained or reactive rings: combination of C–H activation and ring scission

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