Home Chemistry Heterocyclic Building Blocks Oxazolines (R)-4-Benzyl-2-(Pyridin-2-Yl)-4,5-Dihydrooxazole
Substitution Reactions: Depending on the reagents and conditions, the pyridin-2-yl group or the benzyl group can undergo substitution reactions, where another group replaces one of these groups.
Oxidation/Reduction Reactions: The oxazole ring can be subject to oxidation or reduction, leading to changes in the oxidation state of the compound.
Ring-Opening Reactions: Oxazoles can be opened under acidic or basic conditions, yielding products with an open chain structure.
Cross-Coupling Reactions: The benzyl group can participate in cross-coupling reactions with other organic compounds, such as Suzuki, Heck, or Sonogashira reactions, to form new C-C bonds.
Acylation/Alkylation Reactions: Functional groups like the pyridine ring or the oxazole can be subjected to acylation or alkylation reactions to introduce new substituents.
Cyclization Reactions: Depending on the conditions, the compound may undergo intramolecular cyclization reactions, forming new rings or functional groups.
Hydrogenation Reactions: The compound can be hydrogenated to saturate some or all of the double bonds in the molecule.
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(R)-4-Benzyl-2-(5-bromopyridin-2-yl)-4,5-dihydrooxazole
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(R)-4-Benzyl-2-(5-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
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(R)-4-Benzyl-2-(5-fluoropyridin-2-yl)-4,5-dihydrooxazole
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2-[(4R)-4,5-Dihydro-4-(phenylmethyl)-2-oxazolyl]pyridine
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(R)-4-Benzyl-2-(4-methoxy-6-methylpyridin-2-yl)-4,5-dihydrooxazole
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(R)-4-Benzyl-2-(6-methylpyridin-2-yl)-4,5-dihydrooxazole
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(R)-4-Benzyl-2-(4-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
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