Home Chemistry Heterocyclic Building Blocks Oxazolines (S)-4-Benzyl-2-(Pyridin-2-Yl)-4,5-Dihydrooxazole
Substitution Reactions: The benzyl group can undergo substitution reactions, such as electrophilic aromatic substitution or nucleophilic aromatic substitution.
Acylation and Alkylation: The oxazole ring can undergo acylation or alkylation reactions, where an acyl or alkyl group is added to the ring.
Ring-Opening Reactions: Oxazole rings can be opened under certain conditions, leading to the formation of open-chain compounds.
Amidation and Esterification: The compound contains a nitrogen atom in the pyridine ring and oxygen in the oxazole ring, which can participate in amidation and esterification reactions, respectively.
Grignard Reactions: Depending on the functional groups and reaction conditions, Grignard reagents can be used to modify the compound.
Cyclization Reactions: Depending on the reaction conditions and reagents used, the compound can undergo cyclization reactions to form different ring structures.
Chiral Chemistry: Since the compound is chiral due to the (S)-configuration, it can participate in enantioselective reactions and asymmetric synthesis.
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(S)-4-Benzyl-2-(5-bromopyridin-2-yl)-4,5-dihydrooxazole
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(S)-4-Benzyl-2-(5-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
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(S)-4-Benzyl-2-(4-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
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(S)-4-Benzyl-2-(5-fluoropyridin-2-yl)-4,5-dihydrooxazole
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(S)-4-Benzyl-2-(pyridin-2-yl)-4,5-dihydrooxazole
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(S)-4-Benzyl-2-(4-methoxy-6-methylpyridin-2-yl)-4,5-dihydrooxazole
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(S)-4-Benzyl-2-(6-methylpyridin-2-yl)-4,5-dihydrooxazole
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(S)-4-Benzyl-2-(5-chloropyridin-2-yl)-4,5-dihydrooxazole
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