Controllable chemoselectivity in the reaction of 2H-indazoles with alcohols under visible-light irradiation: synthesis of C3-alkoxylated 2H-indazoles and ortho-alkoxycarbonylated azobenzenes-Reference-Cited by-同舟云学术

Controllable chemoselectivity in the reaction of 2H-indazoles with alcohols under visible-light irradiation: synthesis of C3-alkoxylated 2H-indazoles and ortho-alkoxycarbonylated azobenzenes

Published:2021 Issue:15 Volume:8 Page:4230-4236
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Sun Mingli¹²³⁴⁵,Li Laiqiang¹²³⁴⁵^ORCID,Wang Lei¹²³⁴⁵^ORCID,Huo Jie¹²³⁴,Sun Manman¹²³⁴,Li Pinhua⁵⁶⁷⁴⁸^ORCID

Affiliation:

1. Advanced Research Institute and Department of Chemistry

2. Taizhou University

3. Taizhou

4. P. R. China

5. Department of Chemistry

6. Huaibei Normal University

7. Huaibei

8. State Key Laboratory of Organometallic Chemistry

Abstract

A high chemoselectivity in the visible-light-induced reaction of 2H-indazoles with alcohols controlled by the reaction atmosphere was achieved, providing C3-alkoxylated 2H-indazoles and ortho-alkoxycarbonylated azobenzenes.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO00592H

Reference52 articles.

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2. Oxadiazolylindazole Sodium Channel Modulators are Neuroprotective toward Hippocampal Neurones

3. Indazole Estrogens: Highly Selective Ligands for the Estrogen Receptor β