Ugi-Smiles Access to Quinoxaline Derivatives
- 1 January 2007
- journal article
- Published by The Japan Institute of Heterocyclic Chemistry in HETEROCYCLES
- Vol. 73 (1), 503
- https://doi.org/10.3987/com-07-s(u)26
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- CuI/l-histidine catalyzed N-arylation of heterocyclesJournal of Molecular Catalysis A: Chemical, 2007
- Isolation and characterization of 2-alkylaminobenzo[b]furans. Evidence for competing O-arylation in Cu-catalyzed intramolecular amidationTetrahedron Letters, 2007
- Direct Access to Heterocyclic Scaffolds by New Multicomponent Ugi−Smiles CouplingsOrganic Letters, 2006
- Pd-Catalyzed Intermolecular Amidation of Aryl Halides: The Discovery that Xantphos Can Be Trans-Chelating in a Palladium ComplexJournal of the American Chemical Society, 2002
- Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1,2-diaminesTetrahedron Letters, 2002
- A Rapid Access to Biaryl Ether Containing Macrocycles by Pairwise Use of Ugi 4CR and Intramolecular SNAr-Based CycloetherificationOrganic Letters, 2001
- Applications of N-BOC-diamines for the solution phase synthesis of ketopiperazine libraries utilizing a Ugi/De-BOC/Cyclization (UDC) strategyTetrahedron Letters, 1998
- Multiple-Component Condensation Strategies for Combinatorial Library SynthesisAccounts of Chemical Research, 1996
- The mechanism of action of the anti-herpes virus compound 2,3-dimethyl-6(2-dimethylaminoethyl)-6H-indolo-(2,3-b)quinoxalineAntiviral Research, 1991