Unmasking the elusive 1,4-diazabutatrienes: the stabilizing role of the N-substituents
Author:
Affiliation:
1. Departamento de Química Orgánica
2. Facultad de Química
3. Regional Campus of International Excellence “Campus Mare Nostrum”
4. Universidad de Murcia
5. E-30100 Murcia
Abstract
Challenging 1,4-diazabutatrienes are computed to be more stabilized by substituents with either good π-donor or σ-acceptor capability.
Funder
Fundación Séneca
Ministerio de Economía y Competitividad
Publisher
Royal Society of Chemistry (RSC)
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://pubs.rsc.org/en/content/articlepdf/2021/CP/D1CP00274K
Reference24 articles.
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3. Recent Highlights in Ketenimine Chemistry
4. Tandem 1,5-Hydride Shift/6π Electrocyclization of Ketenimines and Carbodiimides Substituted with Cyclic Acetal and Dithioacetal Functions: Experiments and Computations
5. Tandem 1,5-Hydride Shift/1,5-S,N-Cyclization with Ethylene Extrusion of 1,3-Oxathiolane-Substituted Ketenimines and Carbodiimides. An Experimental and Computational Study
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