A Novel Pseudo-Three-Component Synthetic Strategy for the Synthesis of 1,6-Dihydroazaazulenes via Cyclization of Pyrrolyl-enones
Author:
Affiliation:
1. Laboratorio de Diseño Molecular, Instituto de Investigaciones Químico-Biológicas, Universidad Michoacana de San Nicolás de Hidalgo
2. Universidad de Guanajuato, Campus Guanajuato, Division de Ciencias Naturales y Exactas, Departamento de Química
Abstract
Funder
Consejo Nacional de Ciencia y Tecnología
Coordinación de la Investigación Científica
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/a-1535-6085.pdf
Reference6 articles.
1. Radical cascade cyclization of 1,n-enynes and diynes for the synthesis of carbocycles and heterocycles
2. Total eclipses and the heart Figuring Maria Popova Pantheon, 2019. 592 pp.
3. New Approach to the Synthesis of Non-benzenoid Aromatic Compounds, Functionalized 1-Azaazulene Derivatives: Cyclization Reactions of 2-Substituted Tropones with N-Silylenamine and Enamine
4. Gold-Catalyzed Cascade Reaction of Skipped Diynes for the Construction of a Cyclohepta[b]pyrrole Scaffold
5. Pyrrole: An emerging scaffold for construction of valuable therapeutic agents
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Derivates of 1,6-dihyadroazaazulenes as inhibitors of tyrosine kinases BCR-ABL1 wild type and mutant T315I: a molecular dynamics approach;Journal of Biomolecular Structure and Dynamics;2023-11-08
2. Pseudo-multicomponent reactions;RSC Advances;2023
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