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Formation of Thioamide Derivatives from Reactions of Isothiocyanates with Oxazol-2-amines
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inferred← citeshttps://doi.org/10.1002/chin.198532171openalex-snapshot
ChemInform Abstract: Formation of Thioamide Derivatives from Reactions of Isothiocyanates with Oxazol‐2‐amines.
inferred← citeshttps://doi.org/10.1002/jhet.5570290617openalex-snapshot
Electrophilic substitution of diazonium salts in 2‐amino‐4‐(alkyl or aryl)oxazoles
inferred← citeshttps://doi.org/10.1002/jhet.5570340237openalex-snapshot
Friedel‐crafts reactions of 2‐amino‐4‐(alkyl or aryl)oxazoles with acid chlorides and acid anhydrides: Synthesis of 5‐acyl‐2‐amino‐4‐alkyloxazoles
inferred← citeshttps://doi.org/10.1002/jhet.5570340241openalex-snapshot
A new and facile synthesis of imidazo[2,1‐b]oxazoles
inferred← citeshttps://doi.org/10.1002/jhet.5570450529openalex-snapshot
Phenacyl esters of acetic acid derivatives and their application for the synthesis of 2‐oxo‐4‐phenyl‐5‐(phenylhydrazono)‐2,5‐dihydro‐furan‐3‐derivatives
inferred← citeshttps://doi.org/10.1002/recl.19941130504openalex-snapshot
Synthesis of 4‐imidazolin‐2‐ones from α‐bromo ketimines
inferred← citeshttps://doi.org/10.1007/bf00962046openalex-snapshot
Br2-B(OMe)3-MeOH system for the ?-monobromination of ketones
inferred← citeshttps://doi.org/10.1007/bf00962154openalex-snapshot
Br2-CO(NH2)2-AcOH system for the highly selective ?-monobromination of ketones
inferred← citeshttps://doi.org/10.1007/bf02251618openalex-snapshot
Cyclization of α- and β-amino ketones. (Review)
inferred← citeshttps://doi.org/10.1016/0022-328x(94)80086-3openalex-snapshot
A novel product pattern in the palladium(II)-catalyzed decomposition of a (1-diazo-2-oxoalkyl)silane
inferred← citeshttps://doi.org/10.1016/0969-8043(96)00019-xopenalex-snapshot
Synthesis of [11C]cyanamide, a versatile synthon for the production of 11C-labelled radiopharmaceuticals
inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/00186-2openalex-snapshot
Thionoamides and Their Selenium and Tellurium Analogues
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.08.048openalex-snapshot
Structure–activity relationships of 2-aminothiazoles effective against Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1016/j.bmcl.2014.09.067openalex-snapshot
ΔF508-CFTR correctors: Synthesis and evaluation of thiazole-tethered imidazolones, oxazoles, oxadiazoles, and thiadiazoles
inferred← citeshttps://doi.org/10.1016/j.tet.2022.132836openalex-snapshot
Multicomponent synthesis of allomaltol containing 2-aminooxazoles and acid-catalyzed recyclization into substituted furo[3,2-b]pyrans
inferred← citeshttps://doi.org/10.1021/jm020044dopenalex-snapshot
Novel p53 Inactivators with Neuroprotective Action: Syntheses and Pharmacological Evaluation of 2-Imino-2,3,4,5,6,7-hexahydrobenzothiazole and 2-Imino-2,3,4,5,6,7-hexahydrobenzoxazole Derivatives
inferred← citeshttps://doi.org/10.1023/a:1010477022450openalex-snapshot
Synthesis of 2-Aminothiazole Derivatives
inferred← citeshttps://doi.org/10.1080/10426500008042074openalex-snapshot
RING TRANSFORMATION OF 3-(2-OXOPROPYL)-2(3H)-BENZOTHIAZOLONE IN REACTION WITH PRIMARY AMINE
inferred← citeshttps://doi.org/10.1080/17415990701753407openalex-snapshot
Reactions of thianthrene cation radical tetrafluoroborate with aldehydes: formation of α-(5-thianthreniumyl)aldehyde tetrafluoroborates – a facile synthesis of α-ketols through Lobry de Bruyn–van Ekenstein rearrangement
inferred← citeshttps://doi.org/10.3390/81100793openalex-snapshot
The Chemistry of α-Haloketones and Their Utility in Heterocyclic Synthesis
inferred← citeshttps://doi.org/10.3987/com-18-s(f)22openalex-snapshot
Palladium-Catalyzed Arylation of N-Aminoimidazol-2-ones towards Synthesis of Constrained Phenylalanine Dipeptide Mimics
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