124804-06-4

Upstream product

• 2744-05-0 8-oxabicyclo[4.3.0]non-3-en-9-one 
• 124804-04-2 (3aRS,5RS,6SR,7aSR)-5,6-dihydroxy-perhydro-isobenzofuranon 
• 100-52-7 benzaldehyde 

Downstream Products

• 124804-11-1 4a-Trideuteromethyl-2-phenyl-1,3-dioxolo<4,5-f>perhydroisobenzofuran-5-on 
• 139881-98-4 (3aRS,4aSR,7aRS,8aSR)-2-Phenyl-4a-phenylselenyl-1,3-dioxolo<4.5-f>perhydro-isobenzofuran-5-on 
• 139882-01-2 (3aRS,7aSR,8aSR)-2-Phenyl-1,3-dioxolo<4.5-f>-3a,7a,8,8a-tetrahydroisobenzofuran-5-on 
• 139903-64-3 (3aRS,8aSR)-2-Phenyl-1,3-dioxolo<4,5-f>-3a,4,8,8a-tetrahydroisobenzofuran-5-on 
• 124804-10-0 (3aRS,4aSR,7aRS,8aSR)-4a-Methyl-2-phenyl-1,3-dioxolo<4.5-f>perhydro-isobenzofuran-5-on 
• 139881-99-5 (3aRS,4aSR,7aRS,8aSR)-4a-Brom-2-phenyl-1,3-dioxolo<4,5-f>perhydroisobenzofuran-5-on 

Relevant academic research and scientific papers

Synthesis and Determination of Configuration of a Potential Antimicrobial 5,6-Dihydroxyisobenzofuranone

Isobenzofuranone 3 was prepared by KMnO4-oxidation of 2. 3 was reacted to give acetals 4-10, which adopt the boat-conformation. 3 and its acylated derivatives 11-13 on the other hand prefer the chair-conformation.The relative configurations of 3-13 at the