90719-41-8

Upstream product

• 910247-16-4 (4S)-3-((Z)-7-bromo-5-methylhept-5-enoyl)-4-benzyl-2-oxazolidinone 
• 90719-27-0 (S)-3-acryloyl-4-benzyloxazolidin-2-one 
• 78-79-5 isoprene 
• 90719-32-7 (S)-4-Benzyl-2-oxazolidinone 

Downstream Products

• 141484-13-1 (+)-(1R)-N,4-dimethyl-N-(4-methyl-3-pentenyl)-3-cyclohexenamine 
• 141484-12-0 (+)-(1R)-N,4-dimethyl-N-(4-methyl-3-cyclohexenyl)-3-pentenamide 
• 141484-10-8 (-)-(1R)-N,4-dimethyl-3-cyclohexenamine 
• 121424-36-0 (+)-(1R)-4-methyl-cyclohex-3-enecarboxylic acid 
• 7785-53-7 4R-α-terpineol 
• 90719-47-4 phenylmethyl-(4R)-1-methylcyclohexene-4-carboxylate 

Relevant academic research and scientific papers

Silent catalytic promiscuity in the high-fidelity terpene cyclase δ-cadinene synthase

δ-Cadinene synthase (DCS) is a high-fidelity sesquiterpene synthase that generates δ-cadinene as the sole detectable organic product from its natural substrate (E,E)-FDP. Previous work with this enzyme using substrate analogues revealed the ability of DCS

Enantioselective synthesis of α-terpineol and nephthenol by intramolecular acyloxazolidinone enolate alkylations

Enolate anions generated from norterpenyl bromides bearing oxazolidinone chiral auxiliaries at the chain termini underwent efficient, stereo-biased cyclizations to form 6- and 14-membered rings in novel synthetic routes to α-terpineol and nephthenol enantiomers. The Royal Society of Chemistry 2006.