Reaction of Aryl Isothiocyanate with Pyridines and Dialkyl Acetylenedicarboxylates to Afford Novel Heterocycles-Reference-Cited by-同舟云学术

Reaction of Aryl Isothiocyanate with Pyridines and Dialkyl Acetylenedicarboxylates to Afford Novel Heterocycles

Published:2013-08 Issue:8 Volume:37 Page:455-457
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Hassanabadi Alireza¹,Zhiani Rahele²

Affiliation:

1. Department of Chemistry, Zahedan Branch, Islamic Azad University, PO Box 98135-978, Zahedan, Iran

2. Department of Chemistry, Neyshabur Branch, Islamic Azad University, Neyshabur, Iran

Abstract

The reactive intermediate produced in the reaction between pyridines and dialkyl acetylenedicarboxylates was trapped by aryl isothiocyanates to afford 2-thioxo-1,9a-dihydro-2 H-pyrido [1,2, a]pyrimidine derivatives in good yields.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/174751913X13726957255037

Reference12 articles.

1. The Application of Multi-Component Reactions in Drug Discovery

2. Multiple-Component Condensation Strategies for Combinatorial Library Synthesis

3. Advances in Indolizine Chemistry

4. Bicyclic 6-6 Systems with One Ring Junction Nitrogen Atom: One Extra Heteroatom 1:0

5. Discovering risperidone: the LSD model of psychopathology

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2. Synthesis of 2-Selanylidene-1,9A-Dihydro-2H-Pyrido[1,2-A]Pyrimidine Derivatives;Journal of Chemical Research;2018-07

3. ChemInform Abstract: Reaction of Aryl Isothiocyanate with Pyridines and Dialkyl Acetylenedicarboxylates to Afford Novel Heterocycles (IV).;ChemInform;2014-01-31