An efficient strategy for synthesis of new functionalized furo[3,2‐ <i>c</i> ]pyridin‐4( <scp>5</scp> <i>H</i> )‐one derivatives under mild conditions-Reference-Cited by-同舟云学术

An efficient strategy for synthesis of new functionalized furo[3,2‐ c ]pyridin‐4( 5 H )‐one derivatives under mild conditions

Published:2022-06-02 Issue:10 Volume:59 Page:1742-1751
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:Journal of Heterocyclic Chem

Author:

Tao Jiahao¹,Li Chunmei¹²,Zhou Kaini¹,Huan Yongcan¹,Yuan Yongjie¹,Liu Ali¹,Zhang Furen¹^ORCID,Qi Chenze¹,Shen Zhenlu²

Affiliation:

1. School of Chemistry and Chemical Engineering, Zhejiang Key Laboratory of Alternative Technologies for Fine Chemicals Process Shaoxing University Shaoxing China

2. College of Chemical Engineering Zhejiang University of Technology Hangzhou China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.4502

Reference43 articles.

1. Elaboration of Furopyridine Scaffolds

2. Charting the Chemical Reactivity Space of 2,3-Substituted Furo[2,3-b]pyridines Synthesized via the Heterocyclization of Pyridine-N-oxide Derivatives

3. Anion Relay Enabled [3 + 3]-Annulation of Active Methylene Isocyanides and Ene-Yne-Ketones

4. Concise, gram-scale synthesis of furo[2,3-b]pyridines with functional handles for chemoselective cross-coupling

5. Intramolecular azavinyl carbene-triggered rearrangement of furans

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