The origin of experimental regioselectivity in ring-closing reaction of pyrido[1,2-<i>e</i>]purine systems and comparison of the aromaticity character of probable products: a mechanistic study based on DFT insights-Reference-Cited by-同舟云学术

The origin of experimental regioselectivity in ring-closing reaction of pyrido[1,2-e]purine systems and comparison of the aromaticity character of probable products: a mechanistic study based on DFT insights

Published:2023 Issue:23 Volume:47 Page:11123-11133
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Moghimi Parvin¹^ORCID,Bolourian Shadi²,Shiri Ali¹^ORCID,Eshghi Hossein¹^ORCID,Hosseini Fereshteh²,Sabet-Sarvestani Hossein²^ORCID

Affiliation:

1. Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad, Mashhad, Iran

2. Department of Food Additives, Food Science and Technology Research Institute, Research Center for Iranian Academic Center for Education, Culture and Research (ACECR), Khorasan Razavi Branch, Mashhad, Iran

Abstract

Investigation of the regioselectivity, mechanistic aspects and aromaticity character of hydrazine derivatives of pyrido[1,2-e]purine in a ring-closing reaction is the main purpose of this study.

Funder

Academic Center for Education, Culture and Research

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/NJ/D3NJ01276J

Reference68 articles.

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2. J.Cornelisse , Aromaticity and Antiaromaticity. Electronic and Structural Aspects V.I. Minkin, M.N. Glukhovtsev and B.Ya. Simkin John Wiley & Sons, Inc., New York, 1994 313 pp., £66.00 ISBN 0-471-59382-6, 1995

3. Unusual reactivity of small cyclophanes: nucleophilic attack on 11-chloro- and 8,11-dichloro[5]metacyclophane

4. What is aromaticity?

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