Home Chemistry Heterocyclic Building Blocks Isoxazoles N-((5R,6R)-7-Oxo-4-Thia-1-Azabicyclo[3.2.0]Heptan-6-Yl)-3-Phenylisoxazole-4-Carboxamide
Amide Hydrolysis: The amide bond in the molecule can undergo hydrolysis when treated with strong acids or bases to yield the corresponding carboxylic acid and amine.
Reduction: The carbonyl groups in the molecule can be reduced to alcohols or hydrocarbons using reducing agents such as lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4).
Nucleophilic Substitution: The molecule contains several potentially electrophilic carbonyl groups that can undergo nucleophilic substitution reactions with various nucleophiles, including amines, alcohols, and hydrazines.
Cycloaddition Reactions: Depending on the conditions and reagents, the molecule may participate in cycloaddition reactions like Diels-Alder reactions or other [3+2] or [4+2] cycloadditions.
Functional Group Transformations: Various functional group transformations such as acylation, alkylation, and halogenation can be performed on this molecule to introduce or modify specific functional groups.
Oxidation Reactions: The sulfur atom in the thia ring can potentially undergo oxidation reactions to convert it to a sulfoxide or sulfone.
Cross-Coupling Reactions: If the molecule contains suitable leaving groups or can be modified to have them, it may undergo cross-coupling reactions such as Suzuki-Miyaura, Heck, or Sonogashira reactions.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :