86504-35-0

Upstream product

• 201230-82-2 carbon monoxide 
• 6485-40-1 (R)-Carvone 
• 131569-57-8 (E)-3-[(1R,4R)-4-Methyl-3-(tetrahydro-pyran-2-yloxy)-cyclohexyl]-but-2-enoic acid methyl ester 
• 131569-58-9 3-[(1R,4R)-4-Methyl-3-(tetrahydro-pyran-2-yloxy)-cyclohexyl]-butyric acid methyl ester 
• 38049-24-0 1-[(1R,4R)-4-Methyl-3-(tetrahydro-pyran-2-yloxy)-cyclohexyl]-ethanone 
• 38049-25-1 2-((2R,5R)-5-Isopropenyl-2-methyl-cyclohexyloxy)-tetrahydro-pyran 
• 131569-59-0 3-[(1R,4R)-4-Methyl-3-(tetrahydro-pyran-2-yloxy)-cyclohexyl]-butan-1-ol 
• 5524-05-0 (2R,5R)-5-isopropenyl-2-methylcyclohexanone 
• 3792-53-8 2-methyl-5-(prop-1-en-2-yl)cyclohexanone 
• 5524-05-0 (+)-dihydrocarvone 

Relevant academic research and scientific papers

Rh-catalyzed selective synthesis of 1,5-dimethylhexahydro-1H-inden-4(2H)-one via hydroformylation of (R)-carvone

This work reports domino hydroformylation, hydrogenation and intramolecular keto-aldol condensation reactions for the selective synthesis of 1,5-dimethylhexahydro-1H-inden-4(2H)-one obtained from (R)-carvone and dihydrocarvone under homogeneous hydroformy

Studies on the Liverwort Sesquiterpene Alcohol Tamariscol. Synthesis and Absolute Configuration

The relative configuration of the liverwort sesquiterpene alcohol (-)-tamariscol 1 has been confirmed by total synthesis and the absolute configuration has been established from the CD spectrum of the hydrindanone degradation product from (-)-1.

Hydroformylation of chiral terpenes with PtCl(SnCl3)-(bis-phosphine) as catalyst

(+)-R-Limonene and (-)-R-carvone undergo hydroformylation in the presence of catalytic Pt-bisphosphine-SnCl2 systems to yield exclusively the linear products.The internal double bond and the carbonyl group remain intact in both substrates during the react

Absolute Configuration and Synthesis of the Liverwort Sesquiterpene Alcohol Tamariscol

The relative configuration of the liverwort sesquiterpene alcohol (-)-tamariscol (1) has been confirmed by total synthesis and its absolute configuration has been established from the CD spectrum of the hydrindanone degraded from (-)-(1).

Cyclic keto-butyraldehydes a process for their preparation, and their use in the preparation of cyclic diisocyanates

New cyclic keto-butyraldehydes of the formula STR1 in which R1 and R2 are either identical or different and denote hydrogen or lower alkyl and in which the cycloaliphatic ring may contain a double bond, can be prepared from the corre