Reaction Mechanism of Vinamidinium Salts and Cyanoacetamide Derivatives-Reference-Cited by-同舟云学术

Reaction Mechanism of Vinamidinium Salts and Cyanoacetamide Derivatives

Published:2015-01 Issue:1 Volume:39 Page:41-43
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Yang Jiabin¹,Su Guoqiang²,Ren Yu²,Chen Yang¹

Affiliation:

1. State Key Laboratory of Bioelectronics, School of Biological Science & Medical Engineering, Southeast University, Nanjing, Jiangsu 210096, P.R. China

2. Nanjing Zhongrui Pharmaceutical Co., Ltd., Nanjing, Jiangsu 211100, P.R. China

Abstract

The mechanism of formation of a pyridin-2(1H)-one synthesised from vinamidinium salts and cyanoacetamide derivatives is illustrated through the preparation and characterisation of a key intermediate.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/174751915X14197029812826

Reference20 articles.

1. An efficient copper-catalyzed coupling reaction of pyridin-2-ones with aryl and heterocyclic halides based on Buchwald's protocol

2. An improved Ullmann–Ukita–Buchwald–Li conditions for CuI-catalyzed coupling reaction of 2-pyridones with aryl halides

3. Divergent synthesis of arylated pyridin-2(1H)-one derivatives via metal-catalysed cross-coupling processes

4. A Practical, Laboratory-Scale Synthesis of Perampanel

5. Discovery of Aryl Aminoquinazoline Pyridones as Potent, Selective, and Orally Efficacious Inhibitors of Receptor Tyrosine Kinase c-Kit

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