Controllable Synthesis of <i>N</i>-Heterocycles via Hydride Transfer Strategy-Enabled Formal [5 + 1] and [5 + 2] Cyclizations-Reference-Cited by-同舟云学术

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Controllable Synthesis of N-Heterocycles via Hydride Transfer Strategy-Enabled Formal [5 + 1] and [5 + 2] Cyclizations

Published:2023-12-28 Issue:1 Volume:26 Page:332-337
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Dong Ying¹,Hu Fangzhi¹,Wu Huixin¹,Guo Feng-Wei¹,Wang Liang¹^ORCID,Du Feng-Yu¹^ORCID,Li Shuai-Shuai¹^ORCID

Affiliation:

1. College of Chemistry and Pharmaceutical Sciences, Qingdao Agricultural University, Changcheng Rd. #700, Qingdao 266109, P. R. China

Funder

Natural Science Foundation of Shandong Province

National Natural Science Foundation of China

Talents of High Level Scientific Research Foundation

Support Plan on Science and Technology for Youth Innovation of Universities in Shandong Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c03986

Reference54 articles.

1. Rings in Drugs

2. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals

3. U.S. FDA Approved Drugs from 2015–June 2020: A Perspective

4. N-Aryl-6-methoxy-1,2,3,4-tetrahydroquinolines: A novel class of antitumor agents targeting the colchicine site on tubulin

5. Synthesis of (−)-PNU-286607 by Asymmetric Cyclization of Alkylidene Barbiturates

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