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Antiulcer agents. 2. Gastric antisecretory, cytoprotective, and metabolic properties of substituted imidazo[1,2-a]pyridines and analogs

https://doi.org/10.1021/jm00394a018
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inferred← citeshttps://doi.org/10.2139/ssrn.4524815openalex-extracted
inferred← citeshttps://doi.org/10.1002/9780470187265.ch3openalex-snapshot
Biologically Active Thiophene Derivatives Revisited: 1983–1988
inferred← citeshttps://doi.org/10.1002/9781118686263.ch13openalex-snapshot
Bicyclic Pyridines Containing Ring‐Junction Nitrogen
inferred← citeshttps://doi.org/10.1002/9783527630639.ch5openalex-snapshot
The Asymmetric Reduction of Heterocyclic Ketones – A Key Step in the Synthesis of Potassium‐Competitive Acid Blockers (P‐CABs)
inferred← citeshttps://doi.org/10.1002/ejoc.201901124openalex-snapshot
The Groebke‐Blackburn‐Bienaymé Reaction
inferred← citeshttps://doi.org/10.1002/jhet.3902openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jhet.5570270621openalex-snapshot
Synthesis of derivatives of pyrazino[1,2‐a]pyrimidin‐4‐ones
inferred← citeshttps://doi.org/10.1002/jhet.5570300508openalex-snapshot
Synthesis and biological evaluation of nucleosides containing 8‐amino‐imidazo[1,2‐α]pyrazine as an isosteric replacement for adenine
inferred← citeshttps://doi.org/10.1002/jhet.5570340301openalex-snapshot
Nitration in the imidazo[1,2‐a]pyrazine series. Experimental and computational results
inferred← citeshttps://doi.org/10.1002/jhet.5570420717openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/tcr.202100240openalex-snapshot
Ortho C−H Functionalization of 2‐Arylimidazo[1,2‐ a ]pyridines
inferred← citeshttps://doi.org/10.1007/978-3-030-55454-5_10openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s40242-014-3520-5openalex-snapshot
One-pot copper nanoparticle-catalyzed synthesis of imidazo[1,2-a]pyridines under solvent-free conditions
inferred← citeshttps://doi.org/10.1007/s42823-023-00603-2openalex-snapshot
Design, synthesis and biological studies of tetrazole fused imidazopyridines
inferred← citeshttps://doi.org/10.1016/j.bmc.2007.08.065openalex-snapshot
Preparation of tetrahydroimidazo[2,1-a]isoquinolines and their use as inhibitors of gastric acid secretion
inferred← citeshttps://doi.org/10.1016/j.bmc.2007.09.009openalex-snapshot
Novel imidazo[1,2-a]pyrazine derivatives as potent reversible inhibitors of the gastric H+/K+-ATPase
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.10.055openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmcl.2009.07.002openalex-snapshot
Evaluation of basic, heterocyclic ring systems as templates for use as potassium competitive acid blockers (pCABs)
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.06.143openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cdc.2023.101001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cdc.2023.101092openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cdc.2024.101176openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cdc.2026.101253openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.12.045openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jmgm.2017.10.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2018.07.039openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.poly.2014.03.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.12.077openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.07.106openalex-snapshot
Discovery and application of iminotriphenylphosphorane as a formal aromatic primary amine protecting group
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.09.065openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0065-7743(08)60860-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0065-7743(08)61593-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0079-6468(08)00203-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0079-6468(08)70021-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0223-5234(98)80012-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s1386-1425(99)00200-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.7b01714openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02937openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acsomega.9b03127openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo015582xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c3md00278kopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c3ra42046aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c4ob01380hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/np9900700409openalex-snapshot
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inferred← citeshttps://doi.org/10.1070/rc1997v066n03abeh000325openalex-snapshot
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inferred← citeshttps://doi.org/10.1070/rcr4430openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/0968768021000035113openalex-snapshot
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inferred← citeshttps://doi.org/10.1134/s1070428022070119openalex-snapshot
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inferred← citeshttps://doi.org/10.14233/ajchem.2020.22433openalex-snapshot
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inferred← citeshttps://doi.org/10.14233/ajchem.2020.22697openalex-snapshot
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