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References from Synthesis of Heteroannulated Indolopyrazines through Domino N–H Palladium-Catalyzed/Metal-Free Oxidative C–H Bond Activation. Local targets link to admitted publications; unresolved targets remain external evidence.
Pharmacological screening of novel indolo[2,3-b]quinoxaline derivatives
2010 · External reference
Microwave assisted synthesis of new indophenazine 1,3,5-trisubstruted pyrazoline derivatives of benzofuran and their antimicrobial activity
10.1016/j.bmcl.2009.03.161 · 2009 · External reference
Side Chain-Dependent Binding of Antitumor Indoloquinoxaline Derivatives to DNA: Comparative Spectroscopic and Viscometric Measurements
10.1248/cpb.49.44 · 2001 · External reference
Synthesis and Antitumor Properties of N-[2-(Dimethylamino)ethyl]carboxamide Derivatives of Fused Tetracyclic Quinolines and Quinoxalines: A New Class of Putative Topoisomerase Inhibitors
10.1021/jm970044r · 1997 · External reference
Synthesis and cytotoxicity of novel 6H-indolo[2,3-b]quinoxaline derivatives
10.1007/s00044-012-0373-7 · 2013 · External reference
Antiherpesvirus activity and mechanism of action of indolo-(2,3-b)quinoxaline and analogs
10.1128/aac.32.11.1720 · 1988 · External reference
The mechanism of action of the anti-herpes virus compound 2,3-dimethyl-6(2-dimethylaminoethyl)-6H-indolo-(2,3-b)quinoxaline
10.1016/0166-3542(91)90066-z · 1991 · External reference
Highly efficient deep-red organic electrophosphorescent devices with excellent operational stability using bis(indoloquinoxalinyl) derivatives as the host materials
10.1039/c3tc30823e · 2013 · External reference
Solution Processable Indoloquinoxaline Derivatives Containing Bulky Polyaromatic Hydrocarbons: Synthesis, Optical Spectra, and Electroluminescence
10.1021/jo2004764 · 2011 · External reference
Host and Dopant Materials for Idealized Deep-Red Organic Electrophosphorescence Devices
10.1002/adma.201100610 · 2011 · External reference
Synthesis, Spectra, and Theoretical Investigations of the Triarylamines Based on 6H-Indolo[2,3-b]quinoxaline
10.1021/jo1016663 · 2010 · External reference
Synthesis, characterization and charge storage properties of π-biindolo[2,3-b]quinoxaline for solution-processing organic transistor memory
10.1016/j.dyepig.2018.07.011 · 2019 · External reference
Cu doped CdS nanoparticles: A versatile and recoverable catalyst for chemoselective synthesis of indolo[2,3-b]quinoxaline derivatives under microwave irradiation
10.1016/j.molcata.2014.07.022 · 2014 · External reference
Cerium oxide nanoparticle-catalyzed three-component protocol for the synthesis of highly substituted novel quinoxalin-2-amine derivatives and 3,4-dihydroquinoxalin-2-amines in water
10.1039/c4ra00717d · 2014 · External reference
Synthesis of a Masked 2,3-Diaminoindole
10.1021/acs.joc.6b02318 · 2016 · External reference
Palladium-Catalyzed Direct Arylation-Based Domino Synthesis of Annulated N-Heterocycles Using Alkenyl or (Hetero)Aryl 1,2-Dihalides
10.1055/s-0029-1216977 · 2009 · External reference
Domino N-H/C-H bond activation: palladium-catalyzed synthesis of annulated heterocycles using dichloro(hetero)arenes
10.1002/anie.200603833 · 2007 · External reference
Palladium catalyzed synthesis and physical properties of indolo[2,3-b]quinoxalines
10.1039/c4ob00841c · 2014 · External reference
Efficient synthesis of thieno[3,2-b:4,5-b′]diindoles and benzothieno[3,2-b]indoles by Pd-catalyzed site-selective C–C and C–N coupling reactions
10.1039/c2ob26489g · 2012 · External reference
The atom economy--a search for synthetic efficiency
10.1126/science.1962206 · 1991 · External reference
Atom Economy─A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way
10.1002/anie.199502591 · 1995 · External reference
Regioselective Synthesis of Indolopyrazines through a Sequential Rhodium-Catalyzed Formal [3+3] Cycloaddition and Aromatization Reaction of Diazoindolinimines with Azirines
10.1021/acs.joc.8b00115 · 2018 · External reference
Unresolved reference
1994 · External reference
SNH methodology and new approaches to condensed heterocyclic systems
10.1351/pac200476091621 · 2004 · External reference
Nucleophilic aromatic substitution of hydrogen and related reactions
10.1016/j.mencom.2007.09.001 · 2007 · External reference
Nucleophilic Substitution of Hydrogen in Heterocyclic Chemistry
10.1021/cr020086+ · 2004 · External reference
Nucleophilic substitution of hydrogen in electron-deficient arenes, a general process of great practical value
10.1039/b822559c · 2010 · External reference
Unresolved reference
2013 · External reference
Unresolved reference
2013 · External reference
Recent Advances in Direct C–H Functionalization of Pyrimidines
10.1055/s-0036-1589520 · 2018 · External reference
Advances in the chemistry of furazano[3,4-b]pyrazines and their analogues
10.1070/rc2003v072n01abeh000776 · 2003 · External reference
A facile, metal-free, oxidative coupling of new 6-(hetero)aryl-[1,2,5]oxadiazolo[3,4-b]pyrazines with pyrroles, indoles and carbazoles
10.3998/ark.5550190.p009.828 · 2016 · External reference
Reactions of pyrazinium salts with phenols:from σH-adducts to SNH products and transformations into benzo[b]furans
10.1007/s11172-011-0144-5 · 2011 · External reference
9-Ethyl-3-{6-(het)aryl-[1,2,5]oxadiazolo[3,4-b]pyrazin-5-yl}-9H-carbazoles: synthesis and study of sensitivity to nitroaromatic compounds
10.1007/s11172-018-2183-7 · 2018 · External reference
Direct C-C-coupling of ferrocenyl- and cymantrenyllithium with 5-(het)aryl-1,2,5-oxadiazolo[3,4-b]pyrazines
10.1007/s11172-011-0389-z · 2011 · External reference
Direct arylalkenylation of furazano[3,4-b]pyrazines via a new C–H functionalization protocol
10.1016/j.tetlet.2015.02.091 · 2015 · External reference
Arylglyoxal oximes as putative C-nucleophiles in eliminative nucleophilic substitution process
10.1016/j.mencom.2019.05.018 · 2019 · External reference
Discovery of Selective Small-Molecule Inhibitors for the β-Catenin/T-Cell Factor Protein–Protein Interaction through the Optimization of the Acyl Hydrazone Moiety
10.1021/acs.jmedchem.5b00223 · 2015 · External reference
Combination of the Suzuki–Miyaura cross-coupling and nucleophilic aromatic substitution of hydrogen (SNH) reactions as a versatile route to pyrimidines bearing thiophene fragments
10.1016/j.tet.2012.04.095 · 2012 · External reference
Synthesis of fused quinoxalines
10.1070/mc2002v012n02abeh001560 · 2002 · External reference
TsNBr2 Mediated Synthesis of 2-Acylbenzothiazoles and Quinoxalines from Aryl Methyl Ketones under Metal Free Condition
10.1002/slct.201900713 · 2019 · External reference
