77614-30-3

Upstream product

• 50-00-0 formaldehyd 
• 75-09-2 dichloromethane 
• 5989-27-5 D-limonene 
• 7637-07-2 boron trifluoride 
• 7646-78-8 tin(IV) chloride 
• 38142-43-7 (+)-(R)-3-(4-Methyl-3-cyclohexen-1-yl)-3-butensaeuremethylester 

Downstream Products

• 100315-01-3 [3-((R)-4-methyl-cyclohex-3-enyl)-but-3-enyloxy]-methanol 
• 100314-38-3 4-methoxy-2-((R)-4-methyl-cyclohex-3-enyl)-but-1-ene 
• 101170-16-5 4-ethoxy-2-((R)-4-methyl-cyclohex-3-enyl)-but-1-ene 
• 100963-71-1 4-allyloxy-2-((R)-4-methyl-cyclohex-3-enyl)-but-1-ene 
• 6556-48-5 6-((R)-4-methyl-cyclohex-3-enyl)-hepta-3ξ,5ξ-dien-2-one 
• 101891-74-1 benzyl-[3-((R)-4-methyl-cyclohex-3-enyl)-but-3-enyl]-ether 
• 110491-77-5 phthalic acid mono-[3-((R)-4-methyl-cyclohex-3-enyl)-but-3-enyl ester] 
• 16430-77-6 4-(3,5-dinitro-benzoyloxy)-2-((R)-4-methyl-cyclohex-3-enyl)-but-1-ene 
• 77614-31-4 (R)-3-(4-methyl-cyclohex-3-enyl)-but-3-enal 
• 102709-84-2 2-((R)-4-methyl-cyclohex-3-enyl)-4-octanoyloxy-but-1-ene 
• 101447-82-9 4-isovaleryloxy-2-((R)-4-methyl-cyclohex-3-enyl)-but-1-ene 
• 101863-82-5 2-((R)-4-methyl-cyclohex-3-enyl)-4-phenylacetoxy-but-1-ene 
• 103099-34-9 2-((R)-4-methyl-cyclohex-3-enyl)-4-palmitoyloxy-but-1-ene 
• 77647-35-9 (1'R)-(2Z)-3-methyl-3-(4'-methylcyclohexene-3'-yl)-propen-2-al-1 

Relevant academic research and scientific papers

Homolimonenol synthesis over Sn supported mesoporous materials

The synthesis of homolimonenol by Prins condensation of limonene and paraformaldehyde over heterogeneous tin-based catalysts is reported for the first time. The tin supported MCM-41, SBA-15, and KIT-6 materials were prepared by incipient wetness impregnat

First total synthesis of heterocurvistone

The sesquiterpene ketone (±)-heterocurvistone was synthesized in eight steps and 12% overall yield from known methyl R-(+)-3-(4-methyl-3-cyclohexen-1-yl)-3-butenoate, readily available from R-(+)-limonene. The key synthetic step is an oxymercuration-induced cyclization.

INSECT GROWTH REGULATORS-VIII. SYNTHESIS OF A CYCLIC ANALOG OF JUVENILE HORMONE-II

The "true" cyclic analog of JH-II was obtained in a six step synthesis from natural (+)-limonene as starting material.