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Advances in Oxazole Chemistry

1974
Publisher Summary This chapter discusses advances in oxazole chemistry. A significant interest in the chemistry of oxazole was revived in an effort to synthesize penicillin, when this fascinating antibiotic molecule was thought to contain an oxazole ring.
Ram Lakhan, Bela Ternai
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Pyrroles from oxazoles

Chemistry of Heterocyclic Compounds, 2012
AbstractReview: 51 refs.
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Condensation of oxazoles with dienophiles

Tetrahedron, 1969
Abstract Pyridoxine analogues have been synthesized via a Diels—Alder reaction of 5-ethoxyoxazoles with dimethyl maleate followed by reduction. The products on oxidation with manganese dioxide yielded pyridoxal analogues. Pyridoxamine derivatives were obtained by reduction of the pyridoxal oximes. Phosphorylation of the pyridoxamine analogues and the
K. F. Turchin   +5 more
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Gold-Catalyzed Radical-Involved Intramolecular Cyclization of Internal N-Propargylamides for the Construction of 5-Oxazole Ketones.

Journal of Organic Chemistry, 2018
An expedient strategy for the synthesis of 5-oxazole ketones was developed via homogeneous gold catalysis with 4-MeO-TEMPO as an oxidant. The desired 5-oxazole ketones were achieved in decent yields with an excellent functional group compatibility under ...
Hejun An   +4 more
semanticscholar   +1 more source

Synthesis and Properties of Polyfluorinated Oxazoles.

ChemInform, 2005
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
V. F. Cherstkov   +4 more
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A new synthesis of oxazoles

Tetrahedron Letters, 1980
Oxazoles are prepared from the ketoximes in a single pot sequence.
Bhatt, MV, Reddy, Gaddam Subba
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Oxazole and isoxazole: From one-pot synthesis to medical applications

Tetrahedron, 2022
Ajay Thakur   +3 more
semanticscholar   +1 more source

Oxidative Intramolecular 1,2-Amino-Oxygenation of Alkynes under AuI /AuIII Catalysis: Discovery of a Pyridinium-Oxazole Dyad as an Ionic Fluorophore.

Angewandte Chemie, 2017
Oxidative intramolecular 1,2-amino-oxygenation reactions, combining gold(I)/gold(III) catalysis, is reported. The reaction provides efficient access to a structurally unique ionic pyridinium-oxazole dyad with tunable emission wavelengths. The application
Aslam C. Shaikh   +4 more
semanticscholar   +1 more source

Fischer oxazole synthesis

2009
Oxazoles from the condensation of equimolar amounts of aldehyde cyanohydrins and aromatic aldehydes in dry ether in the presence of dry hydrochloric acid.
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An unusual oxazole formation

Journal of Heterocyclic Chemistry, 1990
AbstractThe reaction of 2‐propargyloxybenzamide with strong base has been shown to lead to formation of an oxazole and not a benzoxazepinone as reported. The structure has been confirmed by synthesis.
Jules Freedman, Edward W. Huber
openaire   +3 more sources

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