213913-82-7

Upstream product

• 107-30-2 chloromethyl methyl ether 
• 213913-81-6 2-((S)-1-Hydroxymethyl-5-methyl-hex-4-enyl)-5-methyl-phenol 
• 213913-76-9 (S)-9-[3-(1-Methoxy-1-methyl-ethoxy)-propyl]-3,6,6-trimethyl-8,9-dihydro-5,7-dioxa-benzocycloheptene 
• 213913-80-5 (S)-3,6,6-Trimethyl-9-(4-methyl-pent-3-enyl)-8,9-dihydro-5,7-dioxa-benzocycloheptene 
• 213913-79-2 3-((S)-3,6,6-Trimethyl-8,9-dihydro-5,7-dioxa-benzocyclohepten-9-yl)-propionaldehyde 
• 213913-78-1 3-((S)-3,6,6-Trimethyl-8,9-dihydro-5,7-dioxa-benzocyclohepten-9-yl)-propan-1-ol 
• 213913-75-8 (S)-2-(2-Hydroxy-4-methyl-phenyl)-pentane-1,5-diol 

Downstream Products

• 213913-84-9 1-((S)-1,5-Dimethyl-hex-4-enyl)-2-methoxymethoxy-4-methyl-benzene 
• 70878-71-6 (S)-curcuphenol 
• 213913-83-8 Toluene-4-sulfonic acid (S)-2-(2-methoxymethoxy-4-methyl-phenyl)-6-methyl-hept-5-enyl ester 

Relevant academic research and scientific papers

A new stereocontrolled route to (+)-curcuphenol, a phenolic sesquiterpene from the marine sponge Didiscus flavus

Using a synthetic equivalent of chiral 2-cyclopentenol, (+)- curcuphenol, a cytotoxic bisabolane type sesquiterpene isolated from the marine sponge Didiscus flavus, has been synthesized through a concurrent retro-Diels-Alder reaction and Claisen rearrange