Home Chemistry Heterocyclic Building Blocks Tetrahydrofurans (2R,3S)-2-((Benzoyloxy)Methyl)Tetrahydrofuran-3-Yl Benzoate
Hydrolysis: The ester groups can be hydrolyzed under acidic or basic conditions to produce the corresponding carboxylic acids and alcohols.
Esterification: The compound can undergo esterification reactions with various alcohols and acids to form different ester derivatives.
Cleavage reactions: The compound can be subjected to cleavage reactions, such as ozonolysis or cleavage by specific reagents, to break the molecule into smaller fragments.
Reduction: The carbonyl groups in the esters or the aromatic rings can be reduced to alcohols or saturated hydrocarbons using reducing agents like lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4).
Substitution reactions: The aromatic rings can undergo electrophilic aromatic substitution reactions if appropriate reagents and conditions are used.
Rearrangement reactions: Depending on the reaction conditions and reagents, the molecule may undergo rearrangement reactions, especially if it contains a tetrahydrofuran ring.
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((2R,3R)-3-(Benzoyloxy)-4,4-difluoro-5-hydroxytetrahydrofuran-2-yl)methyl benzoate
                                    
                                
                                        
                                        
                                        
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2-Deoxy-2-fluoro-alpha-D-arabinofuranosyl bromide 3,5-dibenzoate
                                    
                                
                                        
                                        
                                        
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(2R,3S,5R)-5-Chloro-2-(((4-methylbenzoyl)oxy)methyl)tetrahydrofuran-3-yl 4-methylbenzoate
                                    
                                
                                        
                                        
                                        
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(2R,3S)-5-Chloro-2-(((4-methylbenzoyl)oxy)methyl)tetrahydrofuran-3-yl 4-methylbenzoate
                                    
                                
                                        
                                        
                                        
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(2R,3S,5R)-5-Chloro-2-(((4-chlorobenzoyl)oxy)methyl)tetrahydrofuran-3-yl 4-chlorobenzoate
                                    
                                
                                        
                                        
                                        
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1-Chloro-3,5-di(4-chlorbenzoyl)-2-deoxy-D-ribose
                                        
                                        
                                        
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((2R,3R)-3-(Benzoyloxy)-4,4-difluoro-5-((methylsulfonyl)oxy)tetrahydrofuran-2-yl)methyl benzoate
                                    
                                
                                        
                                        
                                        
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((2R,3R,5R)-3-(Benzoyloxy)-4,4-difluoro-5-((methylsulfonyl)oxy)tetrahydrofuran-2-yl)methyl benzoate
                                    
                                
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