Dialkylamino and trialkylammonium groups in close proximity: intra- and intermolecular ways of formation, structural consequences, and properties. A case of metal-free directed <i>ortho</i> alkylation-Reference-Cited by-同舟云学术

Dialkylamino and trialkylammonium groups in close proximity: intra- and intermolecular ways of formation, structural consequences, and properties. A case of metal-free directed ortho alkylation

Published:2022 Issue:36 Volume:46 Page:17140-17144
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Kolupaeva Ekaterina V.¹^ORCID,Ozeryanskii Valery A.¹^ORCID

Affiliation:

1. Department of Organic Chemistry, Southern Federal University, Zorge str. 7, 344090 Rostov-on-Don, Russian Federation

Abstract

All principal approaches to get to quaternised 1,8-bis(dialkylamino)naphthalenes along with their unusual properties are reported for the first time.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ02653H

Reference37 articles.

1. peri Interaction in Naphthalene Derivatives

2. Attractive and repulsive effects in the interactions between electron-rich and electron-deficient groups in peri-substituted naphthalenes

3. Naphthalene derivatives peri-substituted by Group 13 elements

4. Structural studies of peri-interactions and bond formation between electron-rich atomic centres and N-phenylcarboxamides or nitroalkenyl groups

5. Substituent effects on through-space fluorine-19-fluorine-19 coupling in the 1,8-difluoronaphthalene system

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