Home Chemistry Organic Building Blocks Ketones (R)-5-Thia-1-Azabicyclo[4.2.0]Oct-2-En-8-One
Nucleophilic Addition: The double bond in the enone moiety of the compound can undergo nucleophilic addition reactions with various nucleophiles, such as amines, alcohols, or thiols. This can result in the formation of new carbon-carbon or carbon-heteroatom bonds.
Reductive Reactions: The ketone group in the molecule can be reduced to the corresponding alcohol using reducing agents like sodium borohydride or lithium aluminum hydride.
Oxidation: The compound can be oxidized to form various products, depending on the oxidizing agent used. For example, it can be oxidized to form a sulfoxide or sulfone by treatment with appropriate oxidants.
Cyclization Reactions: The compound's structure may allow for intramolecular cyclization reactions under specific conditions, leading to the formation of cyclic products.
Reaction with Electrophiles: The compound can react with electrophilic reagents or species, such as alkylating agents or acylating agents, resulting in the addition of these groups to the molecule.
Rearrangements: Intramolecular rearrangement reactions may take place under certain conditions, leading to the formation of isomeric compounds.
Acid-Catalyzed Reactions: In the presence of acid catalysts, various acid-catalyzed reactions can occur, including acylation or hydrolysis reactions.
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(6R,7R)-7-Amino-3-(methoxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
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(6R,7R)-7-Amino-8-oxo-3-vinyl-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
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