Rationalizing the Substituent Effects in Diels–Alder Reactions of Triazolinediones with Anthracene
Author:
Affiliation:
1. Facultad de Ciencias Básicas, Universidad de Medellín, Carrera 87 no. 30-65, 050026 Medellín, Colombia
Funder
Universidad de Medell?n
Fundaci?n para la promoci?n de la investigaci?n y la tecnolog?a
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jpca.2c04970
Reference72 articles.
1. Triazolinediones as Highly Enabling Synthetic Tools
2. Macromolecular engineering in functional polymers via ‘click chemistry’ using triazolinedione derivatives
3. Diels–Alder and ene reactions of singlet oxygen, nitroso compounds and triazolinediones: transition states and mechanisms from contemporary theory
4. 4-Phenyl-1,2,4-triazolin-3,5-dione: a powerful dienophile
5. Diels–Alder reactions of 4-phenyl-1,2,4-triazoline-3,5-dione
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1. Distortion Rules: Diene Ring Size Effects in Diels‐Alder Reactions with Triazolinediones;ChemistrySelect;2024-01-04
2. Toward metal- and catalyst-free Reactions: Deciphering the substituent and external electric field effects on the Diels-Alder reaction between ethylene and nitrosoethylene;Computational and Theoretical Chemistry;2023-11
3. Combined DFT and Machine Learning Study of the Dissociation and Migration of H in Pyrrole Derivatives;The Journal of Physical Chemistry A;2023-08-24
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