The Chemo-selective Reaction of 2-Amino-N′ -arylbenzohydrazide and Ketonic Acid Catalyzed by Iodine for the Synthesis of Quinazoline Derivatives-Reference-Cited by-同舟云学术

The Chemo-selective Reaction of 2-Amino-N′ -arylbenzohydrazide and Ketonic Acid Catalyzed by Iodine for the Synthesis of Quinazoline Derivatives

Published:2018-06-20 Issue:8 Volume:55 Page:1906-1916
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:J. Heterocyclic Chem.

Author:

Liu Jian-Quan¹,Zhang Wen-Ting¹,Wang Xiang-Shan¹^ORCID

Affiliation:

1. School of Chemistry and Materials Science, Jiangsu Key Laboratory of Green Synthesis for Functional Materials; Jiangsu Normal University; Xuzhou Jiangsu 221116 China

Funder

TAPP

Priority Academic Program Development of Jiangsu Higher education Institutions

NSF of Jiangsu Province

National Natural Science Foundation of China

Publisher

Wiley

Subject

Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.3228/fullpdf

Reference50 articles.

1. 4-Oxo-1,2,3,4-tetrahydroquinazolines. I. Syntheses and pharmacological properties of 2-methyl-3-aryl-4-oxo-1,2,3,4-tetrahydroquinazolines and their 1-acyl derivatives

2. 6-Alkylamino- and 2,3-Dihydro-3‘-methoxy-2-phenyl-4-quinazolinones and Related Compounds: Their Synthesis, Cytotoxicity, and Inhibition of Tubulin Polymerization

3. Novel 7-methoxy-6-oxazol-5-yl-2,3-dihydro-1H-quinazolin-4-ones as IMPDH inhibitors

4. QUINAZOLINONE SULFONAMIDES AS DIURETIC AGENTS

5. The synthesis of 2,3-dihydro-4(1H)-quinazolinone angiotensin II receptor antagonists

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1. Proton‐ and halogen‐induced cyclizations of 2‐(3‐butenyl)quinazolin‐4( 3 H)‐ones in the synthesis of pyrrolo[2,1‐ b ]‐ and pyrrolo[1,2‐ а ]quinazolinone derivatives;Journal of Heterocyclic Chemistry;2022-11-20

2. The PIFA-initiated oxidative cyclization of 2-(3-butenyl)quinazolin-4(3H)-ones – an efficient approach to 1-(hydroxymethyl)-2,3-dihydropyrrolo[1,2-a]quinazolin-5(1H)-ones;Beilstein Journal of Organic Chemistry;2021-11-25