N-Phenyl-1,2,4-triazoline-3,5-dione (PTAD) as a Dienophilic Dinitrogen Equivalent: A Simple Synthesis of 3-Amino-1,2,4-benzotriazines from Arylcarbodiimides-Reference-Cited by-同舟云学术

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N-Phenyl-1,2,4-triazoline-3,5-dione (PTAD) as a Dienophilic Dinitrogen Equivalent: A Simple Synthesis of 3-Amino-1,2,4-benzotriazines from Arylcarbodiimides

Published:2010-02 Issue:4 Volume:2010 Page:694-704
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Alajarin Mateo,Bonillo Baltasar,Marin-Luna Marta,Sanchez-Andrada Pilar,Vidal Angel

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference106 articles.

1. Azodicarbonyl Compounds in Heterocyclic Synthesis

2. 1 2, 4-Triazoline-3,5-Diones

3. For recent examples of using PTAD as an enophile, see:

4. A New Solvent-Dependent Mechanism for a Triazolinedione Ene Reaction

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1. 1,2,4-Triazines and Their Benzo Derivatives;Comprehensive Heterocyclic Chemistry IV;2022

2. 4‐Phenyl‐1,2,4‐Triazoline‐3,5‐Dione;Encyclopedia of Reagents for Organic Synthesis;2021-10-21

3. Cobalt-Catalyzed, Directed Intermolecular C–H Bond Functionalization for Multiheteroatom Heterocycle Synthesis: The Case of Benzotriazine;Organic Letters;2021-07-14

4. Carbodiimide-based synthesis of N-heterocycles: moving from two classical reactive sites to chemical bond breaking/forming reaction;Chemical Society Reviews;2020

5. 3-Substituted Benzo[e][1,2,4]triazines: Synthesis and Electronic Effects of the C(3) Substituent;The Journal of Organic Chemistry;2019-04-19

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