134133-76-9

Upstream product

• 34837-55-3 Phenylselenyl bromide 
• 134233-57-1 (1R,5R,9R,2''R)-5,9-dimethyl-2'-<(tert-butyldimethylsilyl)oxy>-2-(5''-oxotetrahydrofurfuryl)-6,7-benzomorphan 
• 134233-50-4 (1R,5R,9R,2''S)-5,9-dimethyl-2'-<(tert-butyldimethylsilyl)oxy>-2-(5''-oxotetrahydrofurfuryl)-6,7-benzomorphan 
• 134233-49-1 (1R,5R,9R,2''S)-5,9-dimethyl-2'-hydroxy-2-(5''-oxotetrahydrofurfuryl)-6,7-benzomorphan 
• 52079-30-8 (+/-)-normetazocine 
• 58879-36-0 (S)-(+)-γ-iodometil-γ-butirrolattone 
• 134233-55-9 (1R,5R,9R,2''R)-5,9-dimethyl-2'-hydroxy-2-(5''-oxotetrahydrofurfuryl)-6,7-benzomorphan 
• 58879-35-9 (5R)-(iodomethyl)-γ-butyrolactone 

Downstream Products

• 134133-77-0 (S)-5-((2R,6S,11R)-8-Hydroxy-6,11-dimethyl-1,2,5,6-tetrahydro-4H-2,6-methano-benzo[d]azocin-3-ylmethyl)-3-phenylselanyl-dihydro-furan-2-one 
• 134133-77-0 (R)-5-((2R,6S,11R)-8-Hydroxy-6,11-dimethyl-1,2,5,6-tetrahydro-4H-2,6-methano-benzo[d]azocin-3-ylmethyl)-3-phenylselanyl-dihydro-furan-2-one 

Relevant academic research and scientific papers

Electrophilic γ-Lactone κ-Opioid Receptor Probes. Analogues of 2'-Hydroxy-2-tetrahydrofurfuryl-5,9-dimethyl-6,7-benzomorphan Diastereomers

Benzomorphans with an electrophilic group in the nitrogen substituent were prepared as potentially irreversible ligands for the κ-opioid receptor.These were synthesized from products of the reaction of normetazocine with the enantiomers of 5-(iodomethyl)-