Highly diastereoselective synthesis of benzothiazolo[3,2-<i>a</i>]pyridines <i>via</i> [4 + 2] annulation reaction of 2-vinylbenzothiazoles and azlactones-Reference-Cited by-同舟云学术

Highly diastereoselective synthesis of benzothiazolo[3,2-a]pyridines via [4 + 2] annulation reaction of 2-vinylbenzothiazoles and azlactones

Published:2022 Issue:22 Volume:20 Page:4512-4517
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Pan Bin¹,Li Ao¹,Liu Dong¹,Ni QingShan²,Liang Wu³,Du Fei³,Gu Jing¹,Ouyang Qin¹^ORCID

Affiliation:

1. College of Pharmacy, Third Military Medical University, Shapingba, Chongqing 400038, China

2. Biomedical Analysis Center, School of Basic Medical Science, Third Military Medical University, Chongqing, 400038, China

3. College of Pharmacy, Chongqing Medical University, Chongqing 400016, China

Abstract

An highly diastereoselective AgOTf-catalyzed [4 + 2] annulation reaction of 2-vinylbenzothiazoles and azlactones was developed in good to excellent yields.

Funder

National Key Research and Development Program of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB00618A

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