930598-04-2

Upstream product

• 67-56-1 methanol 
• 930597-99-2 1-(2,6-dimethoxy-4-pentylphenyl)prop-2-en-1-ol 
• 930598-00-8 3-(2,6-dimethoxy-4-pentyl-phenyl)-pent-4-enoic acid methyl ester 
• 930598-01-9 2-[1-(2,6-dimethoxy-4-pentylphenyl)allyl]-5-methyl-5-hexenoic acid methyl ester 
• 930597-96-9 dimethyl [1-(2,6-dimethoxy-4-pentylphenyl)allyl]malonate 

Downstream Products

• 43009-38-7 (6aS,10aR)-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-ol 
• 488787-51-5 (3R,4R)-3-[(2-hydroxy-6-methoxy-4-pentyl)phenyl]-1-methyl-4-[(1-methyl-1-triethylsilyloxy)ethyl]-1-cyclohexene 
• 36403-68-6 D1,2-Tetrahydrocannabinol methyl ether 
• 1972-08-3 dronabinol 
• 930598-05-3 2-[2-(2,6-dimethoxy-4-pentylphenyl)-4-methyl-cyclohex-3-enyl]-2-propanol 
• 930597-95-8 methyl (1R,2R)-2',6'-dimethoxy-5-methyl-4'-pentyl-1,2,3,4-tetrahydro-[1,1'-biphenyl]-2-carboxylate 

Relevant academic research and scientific papers

Stereodivergent total synthesis of Δ9-tetrahydrocannabinols

All four stereoisomers of Δ9-tetrahydrocannabinol (Δ9-THC) were synthesized in concise fashion using stereodivergent dual catalysis. Thus, following identical synthetic sequences and applying identical reaction conditions to the same

Synthesis of (-)-Δ9-trans-tetrahydrocannabinol: Stereocontrol via mo-catalyzed asymmetric allylic alkylation reaction

(Chemical Equation Presented) Δ9-THC is synthesized in enantiomericaly pure form, where all of the stereochemistry is derived from the molybdenum-catalyzed asymmetric alkylation reaction of the extremely sterically congested bis-ortho-substitut