Home Chemistry Heterocyclic Building Blocks Pyridines 4-(Tert-Butyl)-2-(Pyridin-2-Yl)-4,5-Dihydrooxazole
Aromatic substitution: The pyridine ring can undergo electrophilic aromatic substitution reactions, such as nitration, halogenation, or Friedel-Crafts reactions.
Nucleophilic substitution: The pyridine ring can also undergo nucleophilic aromatic substitution reactions, where it can act as a nucleophile to replace a leaving group.
Ring-opening reactions: The oxazole ring can undergo ring-opening reactions with appropriate reagents.
Alkylation and acylation: The compound may participate in alkylation or acylation reactions, especially at sites where the tert-butyl group does not hinder the reaction.
Oxidation or reduction reactions: The oxazole ring may be susceptible to oxidation or reduction under certain conditions.
Heterocyclic chemistry: The compound may participate in various reactions typical of heterocyclic compounds, such as cyclization, rearrangements, or condensations.
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(R)-2-(5-Bromopyridin-2-yl)-4-(tert-butyl)-4,5-dihydrooxazole
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(S)-4-(tert-Butyl)-2-(5-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
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(S)-4-(tert-Butyl)-2-(4-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
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(S)-4-tert-Butyl-2-(2-pyridyl)oxazoline
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(R)-4-(tert-Butyl)-2-(4-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
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(S)-2-(5-Bromopyridin-2-yl)-4-(tert-butyl)-4,5-dihydrooxazole
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(R)-4-(tert-Butyl)-2-(5-chloropyridin-2-yl)-4,5-dihydrooxazole
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(S)-4-(tert-Butyl)-2-(5-chloropyridin-2-yl)-4,5-dihydrooxazole
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(R)-4-(tert-Butyl)-2-(5-fluoropyridin-2-yl)-4,5-dihydrooxazole
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(R)-4-(tert-Butyl)-2-(4-methoxy-6-methylpyridin-2-yl)-4,5-dihydrooxazole
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(R)-4-(tert-Butyl)-2-(5-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
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(S)-4-(tert-Butyl)-2-(6-methylpyridin-2-yl)-4,5-dihydrooxazole
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(R)-4-(tert-Butyl)-2-(6-methylpyridin-2-yl)-4,5-dihydrooxazole
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