CsF-Catalyzed Transannulation Reaction of Oxazolones: Diastereoselective Synthesis of Diversified trans-N-(6-Oxo-1,4,5,6-tetrahydropyrimidin-5-yl)benzamides with Arylidene Azlactones and Amidines-Reference-Cited by-同舟云学术

CsF-Catalyzed Transannulation Reaction of Oxazolones: Diastereoselective Synthesis of Diversified trans-N-(6-Oxo-1,4,5,6-tetrahydropyrimidin-5-yl)benzamides with Arylidene Azlactones and Amidines

Published:2018-04-24 Issue:6 Volume:20 Page:358-365
ISSN:2156-8952
Container-title:ACS Combinatorial Science
language:en
Short-container-title:ACS Comb. Sci.

Author:

Parhizkar Golnaz¹,Khosropour Ahmad Reza¹^ORCID,Mohammadpoor-Baltork Iraj¹^ORCID,Parhizkar Elahehnaz²,Amiri Rudbari Hadi¹

Affiliation:

1. Department of Chemistry, University of Isfahan, Isfahan 81746-73441, Iran

2. Department of Pharmaceutics, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz 71468-64685, Iran

Funder

Research Council, University of Isfahan

Center of Excellence of Chemistry

Publisher

American Chemical Society (ACS)

Subject

General Chemistry,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/acscombsci.8b00027

Reference38 articles.

1. Synthesis of substituted 2-amino-5,6-dihydropyrimidin-4-ones using an aza-Wittig reaction

2. Recent applications of multicomponent reactions in medicinal chemistry

3. Synthesis and Evaluation of 1,2,4-Triazolo[1,5-a]pyrimidines as Antibacterial Agents Against Enterococcus faecium

4. Biologically active dihydropyrimidones of the Biginelli-type — a literature survey

5. 1-Sulfopyridinium chloride: Green and expeditious ionic liquid for the one-pot synthesis of fused 3,4-dihydropyrimidin-2(1H)-ones and thiones under solvent-free conditions

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