Electrochemical electrophilic bromination/spirocyclization of <i>N</i>-benzyl-acrylamides to brominated 2-azaspiro[4.5]decanes-Reference-Cited by-同舟云学术

Electrochemical electrophilic bromination/spirocyclization of N-benzyl-acrylamides to brominated 2-azaspiro[4.5]decanes

Published:2023 Issue:9 Volume:25 Page:3543-3548
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Zhang Zhongyi¹²,Hou Zhong-Wei¹,Chen Hao¹,Li Pinhua²^ORCID,Wang Lei¹²³^ORCID

Affiliation:

1. Advanced Research Institute and College of Pharmaceutical Sciences, Taizhou University, Jiaojiang, Zhejiang, 318000, P. R. China

2. Department of Chemistry, Huaibei Normal University, Huaibei, Anhui 235000, P. R. China

3. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Shanghai 200032, P. R. China

Abstract

An electrochemical electrophilic bromination/spirocyclization of N-benzyl-acrylamides to brominated 2-azaspiro[4.5]decanes with 2-bromoethan-1-ol as the brominating reagent has been developed.

Funder

Natural Science Foundation of Zhejiang Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/GC/D3GC00728F

Reference67 articles.

1. Saldedines A and B, Dibromo Proaporphine Alkaloids from a Madagascan Tunicate

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