Design and synthesis of novel pyridinium nitrate-bearing substituted anilines via one-pot tandem reactions-Reference-Cited by-同舟云学术

Design and synthesis of novel pyridinium nitrate-bearing substituted anilines via one-pot tandem reactions

Published:2017-07 Issue:7 Volume:41 Page:384-389
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Huijuan Yang¹,Yujie Ren¹²,Wenqian Xu¹,Ren Li¹

Affiliation:

1. College of Chemical and Environmental Engineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai 201418, P.R. China

2. Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, P.R. China

Abstract

Thirty-two novel 2-amino-1-[3-oxo-3-(substituted-anilino)propyl]pyridinium nitrate derivatives were designed and prepared via one-pot tandem reactions. The structure of the 2-methylanilino derivative was characterised by X-ray crystallographic analysis. In addition, a potential formation mechanism is proposed.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/174751917X14967701766950

Reference15 articles.

1. Thiourea–Quaternary Ammonium Salt Catalyzed Asymmetric 1, 3-Dipolar Cycloaddition of Imino Esters To Construct Spiro[pyrrolidin-3,3′-oxindoles]

2. Quaternary Pyridinium Salts: A Review

3. Design, synthesis, biological evaluation and docking study of 4-isochromanone hybrids bearing N-benzyl pyridinium moiety as dual binding site acetylcholinesterase inhibitors

4. Synthesis and anti-microbial activities of some pyridinium salts with alkoxymethyl hydrophobic group

5. 1,4-dihydropyridines from dithionite reduction of pyridinium salts without electron-withdrawing groups as substituents

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