162238-25-7

Upstream product

• 162084-97-1 Acetic acid (3aR,4R,4aS,7S,7aR,8aR)-4-iodo-2,2,3a-trimethyl-6-oxo-octahydro-furo[2',3':4,5]benzo[1,2-d][1,3]dioxol-7-ylmethyl ester 
• 162084-98-2 Acetic acid (3aS,4aR,7S,7aR,8aR)-2,2,3a-trimethyl-6-oxo-octahydro-furo[2',3':4,5]benzo[1,2-d][1,3]dioxol-7-ylmethyl ester 
• 162084-93-7 2-((3aR,5S,7aS)-2,2,7a-Trimethyl-3a,4,5,7a-tetrahydro-benzo[1,3]dioxol-5-yl)-propane-1,3-diol 
• 139618-32-9 2-((3aR,5S,7aS)-2,2,7a-Trimethyl-3a,4,5,7a-tetrahydro-benzo[1,3]dioxol-5-yl)-prop-2-en-1-ol 
• 98-88-4 benzoyl chloride 
• 162238-24-6 (3aS,4aR,7S,7aR,8aR)-7-Hydroxymethyl-2,2,3a-trimethyl-hexahydro-furo[2',3':4,5]benzo[1,2-d][1,3]dioxol-6-one 

Downstream Products

• 98751-77-0 (+)-paeonilactone 

Relevant academic research and scientific papers

Enantiospecific Synthesis of (+)-Paeonilactone C and (+)-Paeoniflorigenone from R-(-)-Carvone

The first total syntheses of (+)-paeonilactone C and (+)-paeoniflorigenone, representative monoterpenes of Paeoniae Radix, have been accomplished starting with R-(-)-carvone via lipase catalyzed highly diastereoselective enzymatic acetylation.The latter synthesis also means the first total synthesis of (+)-paeonisuffral, a new monoterpene recently isolated from Moutan Cortex.