Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 54 checked references that resolve
resolves10.1186/1860-5397-2-3EcoScale, a semi-quantitative tool to select an organic preparation based on economical and ecological parameters
resolves10.1021/ar010065mOrigins, Current Status, and Future Challenges of Green Chemistry
resolves10.1039/B711717EGreen chemistry tools to influence a medicinal chemistry and research chemistry based organisation
resolves10.1039/c3cs60241aBio-based solvents: an emerging generation of fluids for the design of eco-efficient processes in catalysis and organic chemistry
resolves10.1016/S0014-827X(99)00010-5Synthesis of 3,6,7-substituted-quinoxalin-2-ones for evaluation of antimicrobial and anticancer activity. Part 2
resolves10.2174/1573406410602060577Synthesis and In Vitro Evaluation of the Anti-Viral Activity of N-[4-(1H(2H)-benzotriazol-1(2)-yl)phenyl]alkylcarboxamides
resolves10.1089/088922200308936Long-Term Exposure of HIV Type 1-Infected Cell Cultures to Combinations of the Novel Quinoxaline GW420867X with Lamivudine, Abacavir, and a Variety of Nonnucleoside Reverse Transcriptase Inhibitors
resolves10.1021/jf504359pDesign, Synthesis, Antifungal, and Antioxidant Activities of (<i>E</i>)-6-((2-Phenylhydrazono)methyl)quinoxaline Derivatives
resolves10.1002/ardp.200700024Synthesis and Antidiabetic Activity of 3,6,7‐Trisubstituted‐2‐(1<i>H</i>‐imidazol‐2‐ylsulfanyl)quinoxalines and Quinoxalin‐2‐yl isothioureas
resolves10.1016/j.ejmech.2016.01.042Synthesis, structure elucidation, DNA-PK and PI3K and anti-cancer activity of 8- and 6-aryl-substituted-1-3-benzoxazines
resolves10.1039/C5OB00791GScreening of quinoline, 1,3-benzoxazine, and 1,3-oxazine-based small molecules against isolated methionyl-tRNA synthetase and A549 and HCT116 cancer cells including an in silico binding mode analysis
resolves10.1124/jpet.110.167007Pharmacological Characterization of Olodaterol, a Novel Inhaled β2-Adrenoceptor Agonist Exerting a 24-Hour-Long Duration of Action in Preclinical Models
resolves10.1248/cpb.c14-003301,4-Benzoxazine-3(4<i>H</i>)-ones as Potent Inhibitors of Platelet Aggregation: Design, Synthesis and Structure–Activity Relations
resolves10.1021/jm00163a0616-Benzoxazinylpyridazin-3-ones: potent, long-acting positive inotrope and peripheral vasodilator agents
resolves10.1021/jm80034483,4-Dihydro-2<i>H</i>-1,4-benzoxazine Derivatives Combining Thrombin Inhibitory and Glycoprotein IIb/IIIa Receptor Antagonistic Activity as a Novel Class of Antithrombotic Compounds with Dual Function
resolves10.1002/adsc.201500774Visible Light‐Induced Radical Cyclization of Ethyl 2‐(<i>N</i>‐Arylcarbamoyl)‐2‐Chloroiminoacetates: Synthesis of Quinoxalin‐2(1<i>H</i>)‐ones
resolves10.1016/j.tet.2011.07.052Designing a sequential Ugi/Ullmann type reaction for the synthesis of indolo[1,2-a]quinoxalinones catalyzed by CuI/l-proline
resolves10.1021/ol101454xPractical Synthesis of Quinoxalinones via Palladium-Catalyzed Intramolecular N-Arylations
resolves10.1002/adsc.201000199Gold(I)‐Catalyzed Cascade for Synthesis of Pyrrolo[1,2‐<i>a</i>:2′,1′‐<i>c</i>]‐/Pyrido[2,1‐<i>c</i>]pyrrolo[1,2‐<i>a</i>]quinoxalinones
resolves10.2298/JSC100410016CAn environmentally benign one-pot synthesis of 1,2-dihydro-1-arylnaphtho[1,2-e][1,3]oxazine-3-one derivatives catalysed by phosphomolybdic acid
resolves10.1007/BF03246067A One-Pot synthesis of 1,2-Dihydro-1-arylnaphtho[1,2-e][1,3]oxazine-3-one Derivatives catalyzed by Perchloric Acid Supported on Silica (HClO4/SiO2) in the absence of solvent
resolves10.3390/molecules17055164Microwave-assisted Solvent-free Synthesis and in Vitro Antibacterial Screening of Quinoxalines and Pyrido[2, 3b]pyrazines
resolves10.1016/j.molcata.2011.08.026Solvent free synthesis of quinoxalines, dipyridophenazines and chalcones under microwave irradiation with sulfated Degussa titania as a novel solid acid catalyst
resolves10.1016/S1872-2067(15)60845-2Efficient solvent-free synthesis of pyridopyrazine and quinoxaline derivatives using copper-DiAmSar complex anchored on SBA-15 as a reusable catalyst
resolves10.1080/00397910903576685Silica-Gel–Catalyzed Efficient Synthesis of Quinoxaline Derivatives Under Solvent-Free Conditions
resolves10.1134/S1070428006110194Simple procedure for preparation of quinoxalin-2(1H)-one 3-[Oxo(cyclo)alkyl(idene)] derivatives
resolves10.1016/j.bmcl.2010.08.076Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: Novel antibacterial agents against Mycobacterium tuberculosis
resolves10.1007/s11178-005-0321-9Chemistry of Acyl(imidoyl)ketenes: IX. Synthesis and Thermolysis of 3-Aroyl-8-chloro-1,2-dihydro-4H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones
resolves10.1039/C6GC90040BGreen chemistry and resource efficiency: towards a green economy
resolves10.1039/B919660ANew one-pot multistep process with multifunctional catalysts: decreasing the E factor in the synthesis of fine chemicals
resolves10.1039/c002721aTowards a greener synthesis of (S)-3-aminobutanoic acid: process development and environmental assessment
resolves10.1039/C6GC00408CSolvent-free synthesis of quaternary α-hydroxy α-trifluoromethyl diazenes: the key step of a nucleophilic formylation strategy
resolves10.1039/C5GC90069G25 years of energy and green chemistry: saving, storing, distributing and using energy responsibly
resolves10.1039/C6DT02257JSynthesis, characterization, biological activity, DNA and BSA binding study: novel copper(
<scp>ii</scp>
) complexes with 2-hydroxy-4-aryl-4-oxo-2-butenoate
resolves10.1107/S0021889895007138<i>PARST</i>95 – an update to <i>PARST</i>: a system of Fortran routines for calculating molecular structure parameters from the results of crystal structure analyses
The 11 references without a DOI — listed, not checked
no DOI — not checkedP. T.
Anastas
and J. C.Warner, Green Chemistry: Theory and Practice, Oxford University Press, 1998
no DOI — not checkedC6GC02893D-(cit5)/*[position()=1]
no DOI — not checkedC6GC02893D-(cit8)/*[position()=1]
no DOI — not checkedC6GC02893D-(cit9)/*[position()=1]
no DOI — not checkedC6GC02893D-(cit13)/*[position()=1]
no DOI — not checkedC6GC02893D-(cit14)/*[position()=1]
no DOI — not checkedC6GC02893D-(cit19)/*[position()=1]
no DOI — not checkedC6GC02893D-(cit20)/*[position()=1]
no DOI — not checkedC6GC02893D-(cit39)/*[position()=1]
no DOI — not checkedC6GC02893D-(cit43)/*[position()=1]
no DOI — not checkedC6GC02893D-(cit58)/*[position()=1]
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