Lewis acid-catalyzed regioselective C–H carboxamidation of indolizines with dioxazolones via an acyl nitrene type rearrangement-Reference-Cited by-同舟云学术

Lewis acid-catalyzed regioselective C–H carboxamidation of indolizines with dioxazolones via an acyl nitrene type rearrangement

Published:2021 Issue:11 Volume:8 Page:2583-2588
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Song Dan¹²³⁴,Huang Changfeng¹²³⁴,Liang Peishi¹²³⁴,Zhu Baofu¹²³⁴,Liu Xiang¹²³⁴,Cao Hua¹²³⁴^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering and Guangdong Cosmetics Engineering & Technology Research Center

2. Guangdong Pharmaceutical University

3. Zhongshan 528458

4. China

Abstract

An efficient, direct, and novel Lewis acid-catalyzed regioselective C–H carboxamidation of indolizines with dioxazolones via an acyl nitrene type rearrangement under metal-free conditions has been documented.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province for Distinguished Young Scholars

Guangdong Pharmaceutical University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO00224D

Reference48 articles.

1. Dioxazolones: Stable Substrates for the Catalytic Transfer of Acyl Nitrenes

2. Front Cover: Nitrene Transfer Reactions for Asymmetric C-H Amination: Recent Development (Eur. J. Org. Chem. 8/2020)

3. Nitrene Radical Intermediates in Catalytic Synthesis

4. Transition-Metal-Catalyzed C–N Bond Forming Reactions Using Organic Azides as the Nitrogen Source: A Journey for the Mild and Versatile C–H Amination

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