90581-54-7

Upstream product

• 56535-98-9 2,5-diphenyl-[1,3]dioxolan-4-one 
• 100-52-7 benzaldehyde 
• 611-71-2 MANDELIC ACID 

Downstream Products

• 90507-56-5 (R)-((R)-2,2-Dimethyl-3-oxo-1-phenyl-propoxy)-phenyl-acetic acid 
• 90507-55-4 (R)-((S)-2,2-Dimethyl-3-oxo-1-phenyl-propoxy)-phenyl-acetic acid 
• 90507-58-7 (R)-Phenyl-((R)-1-phenyl-but-3-enyloxy)-acetic acid 
• 90507-57-6 (R)-Phenyl-((S)-1-phenyl-but-3-enyloxy)-acetic acid 
• 42052-51-7 (S)-3-hydroxy-1,3-diphenyl-propan-1-one 
• 90507-71-4 (R)-(-)-3-phenyl-3-hydroxy-2,2-dimethylpropanal 
• 52178-66-2 (S)-(+)-1-phenyl-2,2-dimethyl-1,3-propanediol 
• 90507-54-3 (R)-((R)-3-Oxo-1,3-diphenyl-propoxy)-phenyl-acetic acid 
• 90507-53-2 (R)-((S)-3-Oxo-1,3-diphenyl-propoxy)-phenyl-acetic acid 

Relevant academic research and scientific papers

Convenient synthesis of O-functionalized mandelic acids via Lewis acid mediated transformation of 1,3-dioxolan-4-ones

An efficient method for the synthesis of O-substituted mandelic acids containing alkenyl, alkynyl, methoxycarbonyl, or phenacyl fragments via the Lewis acid-catalyzed reaction of 1,3-dioxolan-4-ones with different C-nucleophiles is proposed.

Flash Vacuum Thermolysis of 1,3-Dioxolan-4-ones

Flash vacuum thermolysis of 1,3-dioxolane-4-ones yields aldehydes and ketones as the major products as the result of apparent decarboxylation of α lactones formed by collapse of a 1,3 dipole.When phenyl substituents are present, epoxides are also formed via the intermediacy of a carbonyl ylide.