Circular linkage of intramolecular multi-hydrogen bonding frameworks through nucleophilic substitutions of β-dicarbonyls onto cyanuric chloride and subsequent tautomerisation-Reference-Cited by-同舟云学术

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Circular linkage of intramolecular multi-hydrogen bonding frameworks through nucleophilic substitutions of β-dicarbonyls onto cyanuric chloride and subsequent tautomerisation

Published:2020 Issue:64 Volume:10 Page:39033-39036
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Awatani Ayano¹²³⁴,Suzuki Masaaki¹²³⁴^ORCID

Affiliation:

1. Graduate School of Natural Science and Technology

2. Shimane University

3. Matsue

4. Japan

Abstract

Triply β-dicarbonyl-embedded 1,3,5-triazine derivatives result in formation of circular linkage of resonance-assisted hydrogen bonding interactions, which can be regarded as well-delocalized resonance hybrids.

Funder

Japan Society for the Promotion of Science

Electric Technology Research Foundation of Chugoku

Tokuyama Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/RA/D0RA07677E

Reference37 articles.

1. Intramolecular Hydrogen Bonding in Medicinal Chemistry

2. Special Issue: Intramolecular Hydrogen Bonding 2017

3. Introduction to “Intramolecular Hydrogen Bonding 2018”

4. Intramolecular hydrogen bonding: An opportunity for improved design in medicinal chemistry

5. Facile Synthesis of Largemeso-Pentafluorophenyl-Substituted Expanded Porphyrins

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