Home Chemistry Heterocyclic Building Blocks Dioxolanes (3As,6As)-Tetrahydrofuro[3,4-D][1,3]Dioxole
Oxidation: The molecule may undergo oxidation reactions when exposed to strong oxidizing agents. This could lead to the formation of various oxidation products.
Substitution Reactions: Depending on the functional groups present in the molecule, it may undergo substitution reactions. For instance, if there are halogen substituents on the aromatic rings, they can undergo nucleophilic aromatic substitution reactions.
Reduction: The molecule may be reduced using reducing agents to convert certain functional groups to their respective reduced forms.
Esterification: If there are suitable functional groups (e.g., hydroxyl groups), the compound can undergo esterification reactions with carboxylic acids or acid chlorides.
Acid-Catalyzed Reactions: The presence of oxygen and heteroatoms in the molecule can make it susceptible to various acid-catalyzed reactions, such as acetal formation, ketal formation, or hydrolysis.
Nucleophilic Addition: Depending on the specific functional groups present, nucleophilic addition reactions can occur at various positions within the molecule.
Aromatic Chemistry: If the molecule contains aromatic rings, it can participate in typical aromatic reactions, such as electrophilic aromatic substitution.
Lewis Acid/Base Reactions: The molecule may react with Lewis acids or bases, depending on its functional groups and reactivity.
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Methyl-5-deoxy-2,3-o-isopropylidene-d-ribofuranoside
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Methyl 2,3-O-Isopropylidene-β-D-ribofuranoside
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(3aS,4S,6R,6aR)-6-Methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole-4-carboxylic acid
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(3aS,4S,6R,6aR)-4-(Iodomethyl)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole
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Methyl 2,3-O-isopropylidene-D-ribofuranoside
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