99682-63-0

Upstream product

• 100954-88-9 (+/?)-trans-4-chloro-3-phenylisochroman-1-one 
• 78317-99-4 rac-(3S,4R)-4-bromo-3,4-dihydro-3-phenylisochromen-1-one 
• 100954-88-9 (+/-)-cis-4-chloro-3-phenyl-isochroman-1-one 
• 78317-99-4 (+/-)-cis-4-bromo-3-phenyl-isochroman-1-one 
• 64283-88-1 (3RS,4RS)-4-hydroxy-3-phenyl-isochroman-1-one 
• 7664-93-9 sulfuric acid 
• 5079-90-3 (E)-2-styrylbenzoic acid 
• 66374-10-5 (Z)-2-(2-phenylethenyl)benzoic acid 
• 64283-88-1 (+/-)-trans-4-hydroxy-3-phenyl-isochroman-1-one 
• 81428-81-1 Methyl (E)-2-(2-phenylethenyl)benzoate 

Downstream Products

• 93322-21-5 (RS)-3-((SR)-α-acetoxy-benzyl)-phthalide 
• 87-41-2 2-benzofuran-1(3H)-one 
• 100-52-7 benzaldehyde 
• 18398-22-6 3-benzoylisobenzofuran-1(3H)-one 
• 100954-90-3 (RS)-3-((RS)-α-chloro-benzyl)-phthalide 
• 20871-38-9 N,N-dimethyl-2-(phenylacetyl)benzamide 
• 125217-05-2 threo (3RS,8SR)-3-isobenzofuran-1(3H)-one 
• 100954-90-3 (RS)-3-((SR)-α-chloro-benzyl)-phthalide 
• 125217-05-2 erythro (3RS,8SR)-3-isobenzofuran-1(3H)-one 

Relevant academic research and scientific papers

Organocatalytic Synthesis of Lactones by the Oxidation of Alkenoic Acids

Along the lines of modern sustainable oxidation, a green and mild organocatalytic synthetic procedure for the synthesis of hydroxylactones from alkenoic acids is described. The reaction includes the activation of H2O2 by an organocat