Aromatic ring synthesis by -aminopyrrole Diels-Alder reaction. Characterization of the heteroatom fragment
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
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1. Synthesis of highly substituted benzene ring systems through three-component coupling of enyne imines, Fischer carbene complexes, and electron-deficient alkynes;Tetrahedron Letters;2017-04
2. Aminopyrroles;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
3. Chemistry of 7-Azabicyclo[2.2.1]hepta-2,5-dienes, 7-Azabicyclo[2.2.1]hept-2-enes, and 7-Azabicyclo[2.2.1]heptanes;Chemical Reviews;1996-01-01
4. Mild thermal route to phthalimidonitrene and its reaction with activated benzenes to give 2H- and 3H-azepines; X-ray crystal structure analysis of an isolable 2H-azepine;Journal of the Chemical Society, Perkin Transactions 1;1995
5. The utility of the PM3 method for predicting the reactivities of cyanoethenes in diels-alder reactions with pyrrole;Journal of Heterocyclic Chemistry;1994-11
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