Synthesis of Pyrimido[1,2-<i>a</i>]indolediones and Pyrimidinediones via [4+2] Annulation of 2<i>H</i>-Azirine-2-carbaldehydes-Reference-Cited by-同舟云学术

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Synthesis of Pyrimido[1,2-a]indolediones and Pyrimidinediones via [4+2] Annulation of 2H-Azirine-2-carbaldehydes

Published:2024-04-25 Issue:10 Volume:89 Page:7339-7346
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Li Lesong¹,Shi Zhenyu¹,Li Congyang¹,Zhang Xiaoli¹,Zhang Yichi¹,Ren Weiwu¹²^ORCID

Affiliation:

1. Molecular Synthesis Center & Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, 5 Yushan Road, Qingdao 266003, China

2. Laboratory for Marine Drugs and Bioproducts, Laoshan Laboratory, Qingdao 266237, China

Funder

Taishan Scholar Project of Shandong Province

Fundamental Research Funds for the Central Universities

National Natural Science Foundation of China

Qingdao Marine Science and Technology Center

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00654

Reference35 articles.

1. Synthesis of Optically Active Vasicinone Based on Intramolecular Aza-Wittig Reaction and Asymmetric Oxidation1

2. Antiviral Action of Tryptanthrin Isolated from Strobilanthes cusia Leaf against Human Coronavirus NL63

3. Structure Revision of Anti-Inflammatory Indole Alkaloids with a 1,2-Benzisoxazole Ring

4. Luotonin A. A Naturally Occurring Human DNA Topoisomerase I Poison

5. Pyrimidine-2,4-dione targets STAT3 signaling pathway to induce cytotoxicity in hepatocellular carcinoma cells

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