Annulation of imidazolines: A 1,3-dipolar cycloaddition route to pyrroloimidazoles, pyrrolidines and pyrroles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Generation and cycloadditions of tetrahydrofuryl, pyranyl, and oxepanyl-2-imminium methylides
2. New Generation of 1,3-Dipoles from Organosilicon Compounds and Syntheses of Heterocycles
3. Prototropic routes to 1,3- and 1,5-dipoles, and 1,2-ylides: applications to the synthesis of heterocyclic compounds
4. Ylides by the desilylation of .alpha.-silyl onium salts
5. Azomethine Ylids, Azomethine Imines, and Iminophosphoranes in Organic Syntheses
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1. Multi-Ion Bridged Pathway of N-Oxides to 1,3-Dipole Dilithium Oxide Complexes;The Journal of Organic Chemistry;2021-08-11
2. Substituent-directed reduction of cyclic aminals leading to two different heterocycles selectively: syntheses of functionalized nicotines and pyrido[2,3-b]azepines;Tetrahedron;2015-04
3. Selective Reduction and Dehydrogenation of 6-Benzylideneoctahydropyrrolo[1,2-a]Pyrimidines and 5-Benzylidenehexahydropyrrolo[1,2-a]Imidazoles as New Approaches to N-(ω-Aminoalkyl)Pyrrolidines and Bicyclic Amidines;Mendeleev Communications;2013-01
4. 1,3-Dipolar Cycloadditions of Phenanthridinium-Based Azomethine Ylides;Bulletin des Sociétés Chimiques Belges;2010-09-01
5. ChemInform Abstract: Annulation of Imidazolines: A 1,3-Dipolar Cycloaddition Route to Pyrroloimidazoles, Pyrrolidines, and Pyrroles.;ChemInform;2010-08-23
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