Pyrrolo[1,2,3-de]quinoxalines: unexpected products from 1,3-dipolar cycloaddition of dihydroimidazolium ylides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. Annulation of dihydroimidazoles: a 1,3-dipolar cycloaddition route to pyrrolo[1,2-a]imidazoles, pyrrolidines and pyrroles
2. Cycloaddition of homochiral imidazolinium ylides: A route to optically active pyrroloimidazoles
3. An enantioselective route to pyrrolidines: Removal of the chiral template from homochiral pyrroloimidazoles
4. A rapid assembly of homochiral 2,3,4-trisubstituted pyrrolidines
5. See, for example: (a) Richardson, A. J. Org. Chem. 1965, 30, 2589–2593;
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1. Ring-opening reactions of 2-imidazolines and their applications;Advances in Heterocyclic Chemistry;2020
2. ChemInform Abstract: Pyrrolo[1,2,3-de]quinoxalines: Unexpected Products from 1,3-Dipolar Cycloaddition of Dihydroimidazolium Ylides.;ChemInform;2010-05-24
3. The Annulation of 2-Imidazolines;Advances in Heterocyclic Chemistry;2010
4. Construction of Enantiopure Pyrrolidine Ring System via Asymmetric [3+2]-Cycloaddition of Azomethine Ylides;Chemical Reviews;2006-10-25
5. Intramolecular 1,3-dipolar cycloadditions of dihydroimidazolium ylides: synthesis of pyrrolo[1,2,3-de]quinoxalines and imidazo[1,2-a]indoles;Organic & Biomolecular Chemistry;2006
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