Aniline assisted dimerization of phenylalanines: convenient synthesis of 2-aroyl-3-arylquinoline in an I2-DMSO system

Author:

Ma Jin-Tian1,Chen Ting1,Chen Xiang-Long1,Zhou You1,Yu Zhi-Cheng1,Zhuang Shi-Yi1,Wu Yan-Dong1,Xiang Jia-Chen2ORCID,Wu An-Xin1ORCID

Affiliation:

1. Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079, P. R. China

2. School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, China

Abstract

I2-mediated catabolism and reconstruction of amino acids emerges again to furnish 2-aroyl-3-arylquinolines in a convenient way.

Funder

Fundamental Research Funds for the Central Universities

Higher Education Discipline Innovation Project

Natural Science Foundation of Jiangsu Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference60 articles.

1. V. A. Soloshonok and K. Izawa (ed.), Asymmetric Synthesis and Application of α-Amino Acids , American Chemical Society , Washington, DC , 2009 , p. 1009

2. P.Lloyd-Williams , F.Albericio and E.Giralt , Chemical Approaches to the Synthesis of Peptides and Proteins , CRC Press , 1997 , vol. 10 , pp. 1–304

3. Solid Phase Peptide Synthesis. I. The Synthesis of a Tetrapeptide

4. Liquid Phase Synthesis of Peptides

5. The Copper-Catalyzed Decarboxylative Coupling of the sp3-Hybridized Carbon Atoms of α-Amino Acids

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