Home Chemistry Heterocyclic Building Blocks Epoxides 7-Oxabicyclo[4.1.0]Heptane
Ring Opening Reactions: Due to the strained nature of the bicyclic structure, 7-oxabicyclo[4.1.0]heptane can undergo ring-opening reactions to form different compounds. For example, it can react with nucleophiles or electrophiles at the three-membered ring, leading to the formation of open-chain compounds.
Oxidation Reactions: The oxygen atom in the seven-membered ring is susceptible to oxidation. Oxidizing agents such as peracids or permanganate can react with 7-oxabicyclo[4.1.0]heptane to introduce oxygen-containing functional groups.
Reduction Reactions: Conversely, 7-oxabicyclo[4.1.0]heptane can undergo reduction reactions, especially if the oxygen atom is targeted. Reduction with hydride reagents like lithium aluminum hydride (LiAlH4) can lead to the formation of a saturated compound.
Substitution Reactions: The three-membered ring can undergo substitution reactions, where one of its substituents is replaced with another group. This can occur through nucleophilic or electrophilic substitution reactions, depending on the conditions and reagents used.
Acid-Catalyzed Reactions: In the presence of an acid catalyst, 7-oxabicyclo[4.1.0]heptane can undergo various transformations. For instance, it can undergo acid-catalyzed hydration to form an alcohol or be involved in rearrangement reactions.
Photochemical Reactions: Exposure to ultraviolet (UV) light can induce photochemical reactions in organic compounds. 7-Oxabicyclo[4.1.0]heptane may undergo photoreactions that lead to the formation of photoproducts with unique structures.
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1-Methyl-4-(prop-1-en-2-yl)-7-oxabicyclo[4.1.0]heptane
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(2-(7-Oxabicyclo[4.1.0]heptan-3-yl)ethyl)triethoxysilane
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Trimethoxy[2-(7-oxabicyclo[4.1.0]hept-3-yl)ethyl]silane
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7-Oxabicyclo[4.1.0]heptan-3-ylmethyl acrylate
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7-Oxabicyclo[4.1.0]heptan-3-ylmethyl methacrylate
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