71596-71-9

Upstream product

• 51694-22-5 ortho-nitrophenyl selenocyanate 
• 82096-26-2 decahydro-1,3a,5a-trimethyl-cyclopentapentalene-4-methanol 
• 71583-67-0 4-(3-butenyl)-1,2,4,6,7,7a-hexahydro-4,7a-dimethyl-5H-inden-5-one 
• 71583-68-1 1,2,3,3a,5,6,6a,7-octahydro-1,3a,6a-trimethyl-4H-cyclopentinden-4-one 
• 82096-24-0 1,2,3,3a,5,6,6a,7,8,9-decahydro-1,3a,6a-trimethyl-4H-cyclopentinden-4-one 
• 82096-25-1 1,2,3,3a,5,6,6a,7,8,9-decahydro-5-hydroximino-1,3a,6a-trimethyl-4H-cyclopentinden-4-one 
• 71596-70-8 decahydro-1,3a,5a-trimethyl-cyclopentapentalene-4-carboxylic acid methylester 

Downstream Products

• 65372-78-3 isocomene 
• 71629-00-0 (+/-)-isocomene 

Relevant academic research and scientific papers

A total synthesis of (±)-isocomene and (±) β-isocomene by an intramolecular ene reaction

The racemic sesquiterpenes isocomene I and β-isocomene 22 have been synthesized starting from 1,7-octadien-3-one 10 in a stereoselective manner. In the key step 12 → 13 (Scheme 5) the C-7, C-8-bond was formed by an intramolecular thermal ene reaction. Fur

A TOTAL SYNTHESIS OF (+/-)-ISOCOMENE AND (+/-) β-ISOCOMENE BY AN INTRAMOLECULAR ENE REACTION

The racemic sesquiterpenes isocomene 1 and β-isocomene 22 have been synthesized starting from 1,7-octadiene-3-one 10 in a stereoselective manner.In the key step 12 -> 13 (Scheme 5) the C-7, C-8 bond was formed by an intramolecular thermal ene reaction.Fur

A total synthesis of (±)-isocomene and (±) β-isocomene by an intramolecular ene reaction

The racemic sesquiterpenes isocomene I and β-isocomene 22 have been synthesized starting from l,7-octadien-3-one (0 in a stereoselective manner. In the key step 12 →13 (Scheme 5) the C-7, C-8-bond was formed by an intramolecular thermal ene reaction. Furt