Chemistry Heterocyclic Building Blocks Oxazolines 2,2'-(1,3-Diphenylpropane-2,2-Diyl)Bis(4,5-Dihydrooxazole)

2,2'-(1,3-Diphenylpropane-2,2-Diyl)Bis(4,5-Dihydrooxazole)

Oxidation: The oxazole rings in the compound can potentially undergo oxidation reactions. For example, they can be oxidized to oxazoles or other oxidation products under the influence of strong oxidizing agents like potassium permanganate (KMnO4) or hydrogen peroxide (H2O2). Reduction: Conversely, the oxazole rings can be reduced to dihydrooxazoles or other reduction products using reducing agents like sodium borohydride (NaBH4). Arylation: The phenyl groups in the compound can undergo various arylation reactions, such as the Suzuki coupling or Heck reaction, to introduce different aryl groups onto the molecule. Substitution Reactions: The phenyl groups can also undergo substitution reactions, including electrophilic aromatic substitution or nucleophilic aromatic substitution, depending on the reaction conditions and the reagents used. Hydrolysis: Under acidic or basic conditions, the compound may undergo hydrolysis, breaking the oxazole rings and potentially leading to the formation of carboxylic acids or other hydrolysis products. Metalation Reactions: The compound can react with various organometallic reagents, such as Grignard reagents or organolithium compounds, to form new C-C or C-metal bonds. Cyclization Reactions: Depending on the reaction conditions, the compound may undergo cyclization reactions to form fused or spirocyclic compounds. Cross-Coupling Reactions: If appropriate functional groups are present, the compound can participate in cross-coupling reactions, such as Suzuki-Miyaura, Stille, or Buchwald-Hartwig reactions, to form new carbon-carbon bonds.

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(3Ar,8As)-2-(Pyridin-2-Yl)-3A,8A-Dihydro-8H-Indeno[1,2-D]Oxazole (3As,8Ar)-2-(Pyridin-2-Yl)-3A,8A-Dihydro-8H-Indeno[1,2-D]Oxazole (4R,5S)-4,5-Diphenyl-2-(Pyridin-2-Yl)-4,5-Dihydrooxazole (R)-4-Benzyl-2-(Pyridin-2-Yl)-4,5-Dihydrooxazole (R)-4-Phenyl-2-(Pyridin-2-Yl)-4,5-Dihydrooxazole (S)-4-(Tert-Butyl)-2-(Pyridin-2-Yl)-4,5-Dihydrooxazole (S)-4-Benzyl-2-(Pyridin-2-Yl)-4,5-Dihydrooxazole (S)-4-Isopropyl-2-(Pyridin-2-Yl)-4,5-Dihydrooxazole (S)-4-Phenyl-2-(Pyridin-2-Yl)-4,5-Dihydrooxazole 1,3-Bis(4,5-Dihydrooxazol-2-Yl)Benzene 2,2'-(1,3-Diphenylpropane-2,2-Diyl)Bis(4,5-Dihydrooxazole) 2,2'-(2-Phenylethane-1,1-Diyl)Bis(4,5-Dihydrooxazole) 2,3-Dihydropyrazolo[5,1-B]Oxazole 2,6-Bis(4,5-Dihydrooxazol-2-Yl)Pyridine 2-(6-Benzhydrylpyridin-2-Yl)-4,5-Dihydrooxazole 2-(6-Cyclopropylpyridin-2-Yl)-4,5-Dihydrooxazole 2-(Benzo[B]Thiophen-2-Yl)-4,5-Dihydrooxazole 2-(Pyridin-2-Ylmethyl)-4,5-Dihydrooxazole 2-(Quinolin-2-Yl)-4,5-Dihydrooxazole 2-Phenyl-4,5-Dihydrooxazole 4,4',5,5'-Tetrahydro-2,2'-Bioxazole 4-(Tert-Butyl)-2-(Pyridin-2-Yl)-4,5-Dihydrooxazole 4-Isopropyl-2-(Pyridin-2-Yl)-4,5-Dihydrooxazole Bis((3Ar,8As)-3A,8A-Dihydro-8H-Indeno[1,2-D]Oxazol-2-Yl)Methane Bis((3As,8Ar)-3A,8A-Dihydro-8H-Indeno[1,2-D]Oxazol-2-Yl)Methane Bis(4,5-Dihydrooxazol-2-Yl)Methane

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    (4R,4'R)-2,2'-(1,3-Diphenylpropane-2,2-diyl)bis(4-methyl-4,5-dihydrooxazole)

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    (4R,4'R)-2,2'-(1,3-Diphenylpropane-2,2-diyl)bis(4-methyl-4,5-dihydrooxazole)

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    (S)-4-(tert-Butyl)-2-(2-((R)-4-(tert-butyl)-4,5-dihydrooxazol-2-yl)-1,3-diphenylpropan-2-yl)-4,5-dihydrooxazole

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    A13519682634687-78-697%

    (S)-4-(tert-Butyl)-2-(2-((R)-4-(tert-butyl)-4,5-dihydrooxazol-2-yl)-1,3-diphenylpropan-2-yl)-4,5-dihydrooxazole

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    (4R,4'R)-2,2'-(1,3-Diphenylpropane-2,2-diyl)bis(4-(tert-butyl)-4,5-dihydrooxazole)

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    (4R,4'R)-2,2'-(1,3-Diphenylpropane-2,2-diyl)bis(4-(tert-butyl)-4,5-dihydrooxazole)

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    (4S,4'S)-2,2'-(1,3-Diphenylpropane-2,2-diyl)bis(4-(tert-butyl)-4,5-dihydrooxazole)

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    (4S,4'S)-2,2'-(1,3-Diphenylpropane-2,2-diyl)bis(4-(tert-butyl)-4,5-dihydrooxazole)

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    (4S,4'S)-2,2'-[2-Phenyl-1-(phenylmethyl)ethylidene]bis[4-(1-methylethyl)-4,5-dihydrooxazole

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    (4S,4'S)-2,2'-[2-Phenyl-1-(phenylmethyl)ethylidene]bis[4-(1-methylethyl)-4,5-dihydrooxazole

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