Palladium-catalyzed selective synthesis of 3,4-dihydroquinazolines from electron-rich arylamines, electron-poor arylamines and glyoxalates-Reference-Cited by-同舟云学术

Palladium-catalyzed selective synthesis of 3,4-dihydroquinazolines from electron-rich arylamines, electron-poor arylamines and glyoxalates

Published:2018 Issue:27 Volume:16 Page:5050-5054
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wu Chao¹²³⁴⁵,Wang Jie¹²³⁴,Zhang Xing-Yu¹²³⁴,Jia Guo-Kai¹²³⁴,Cao Zhong⁵⁶⁷⁴,Tang Zilong⁸⁹¹⁰⁴,Yu Xianyong⁸⁹¹⁰⁴,Xu Xinhua¹¹¹²⁷⁴^ORCID,He Wei-Min¹²³⁴¹¹^ORCID

Affiliation:

1. Department of Chemistry

2. Hunan University of Science and Engineering

3. Yongzhou 425100

4. China

5. Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation

6. Changsha University of Science and Technology

7. Changsha

8. Key Laboratory of Theoretical Organic Chemistry and Functional Molecule of Ministry of Education

9. Hunan University of Science and Technology

10. Xiangtan 411201

11. State Key Laboratory of Chemo/Biosensing and Chemometrics

12. Hunan University

Abstract

Palladium-catalyzed selective synthesis of various 3,4-dihydroquinazolines from electron-rich arylamines, electron-poor arylamines and glyoxalates was developed.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB01005F

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2. Synthesis of 2-(alkylamino)-5,6- and -6,7-dihydroxy-3,4-dihydroquinazolines and evaluation as potential dopamine agonists

3. 2-Amino-3,4-dihydroquinazolines as Inhibitors of BACE-1 (β-Site APP Cleaving Enzyme): Use of Structure Based Design to Convert a Micromolar Hit into a Nanomolar Lead

4. Cyclic guanidines as dual 5-HT5A/5-HT7 receptor ligands: Optimising brain penetration

5. Synthesis and adrenergic blocking effects of 2-(alkylamino)-3,4-dihydroquinazolines

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