Synthesis of pyrrolo[1,3]diazepines by a dipolar cycloaddition—retro-Mannich domino reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. Privileged Structures as Leads in Medicinal Chemistry
2. Synthesis of 1,3-dioxo-hexahydropyrido[1,2-c][1,3]diazepine carboxylates, a new bicyclic skeleton formed by ring expansion–RCM methodology
3. A Unique Ring-Expanded Acyclic Nucleoside Analogue that Inhibits Both Adenosine Deaminase (ADA) and Guanine Deaminase (GDA; Guanase): Synthesis and Enzyme Inhibition Studies of 4,6-Diamino-8H-1-hydroxyethoxymethyl-8-iminoimidazo[4,5-e][1,3]diazepine
4. Possible ligand-receptor interactions for NK1 antagonists as observed in their crystal structures
5. Synthesis of a new pyrrolo[1,3]diazepine: 4H-pyrrolo[1,2-a]thieno[2,3-e][1,3]diazepine
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1. 1,3-Diazepines;Comprehensive Heterocyclic Chemistry IV;2022
2. 1,3‐Diazepine Derivatives: Strategies for Synthesis;European Journal of Organic Chemistry;2021-06-26
3. Microwave-mediated Synthesis of Medium Ring-sized Heterocyclic Compounds;Current Microwave Chemistry;2020-08-06
4. Microwave-Assisted Syntheses of Bioactive Seven-Membered, Macro-Sized Heterocycles and Their Fused Derivatives;Molecules;2016-08-09
5. Progress in 1,3-dipolar cycloadditions in the recent decade: an update to strategic development towards the arsenal of organic synthesis;Tetrahedron;2016-03
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