Home Chemistry Heterocyclic Building Blocks Pyrans (S)-2-Phenylchroman-4-One
Aldol Reaction: (S)-2-phenylchroman-4-one can undergo aldol reactions with appropriate reactants and conditions, forming new carbon-carbon bonds between the carbonyl group and an enolate ion. The chirality of the starting compound can be preserved in the product under certain conditions.
Grignard Reaction: (S)-2-phenylchroman-4-one can react with a Grignard reagent (e.g., phenylmagnesium bromide) to form a new carbon-carbon bond at the carbonyl carbon, leading to the formation of a tertiary alcohol.
Acylation: (S)-2-phenylchroman-4-one can undergo acylation reactions with acyl chlorides or anhydrides to form amides or esters, respectively.
Enzymatic Reactions: Depending on the specific functional groups in the molecule, enzymatic reactions may also be possible. Enzymes such as lipases and proteases can catalyze reactions on chiral compounds like (S)-2-phenylchroman-4-one.
Heterocycle Formation: If appropriate reagents are used, (S)-2-phenylchroman-4-one can participate in heterocyclic ring formation reactions.
Nucleophilic Substitution: Depending on the reaction conditions and the nature of the substituents, nucleophilic substitutions may also occur at various positions on the molecule.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :