1058705-71-7

Basic information

• Product Name: [6S,7S,9(1S)]-7-benzyl-9-[1-(dibenzylamino)-2-phenylethyl]bicyclo[4.3.0]non-1⁽⁹⁾-en-8-one
• Synonyms: [6S,7S,9(1S)]-7-benzyl-9-[1-(dibenzylamino)-2-phenylethyl]bicyclo[4.3.0]non-1⁽⁹⁾-en-8-one
• CAS NO: 1058705-71-7
• Molecular Weight: 525.734
• Mol File: 1058705-71-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [6S,7S,9(1S)]-7-benzyl-9-[1-(dibenzylamino)-2-phenylethyl]bicyclo[4.3.0]non-1⁽⁹⁾-en-8-one(CAS DataBase Reference)
• NIST Chemistry Reference: [6S,7S,9(1S)]-7-benzyl-9-[1-(dibenzylamino)-2-phenylethyl]bicyclo[4.3.0]non-1⁽⁹⁾-en-8-one(1058705-71-7)
• EPA Substance Registry System: [6S,7S,9(1S)]-7-benzyl-9-[1-(dibenzylamino)-2-phenylethyl]bicyclo[4.3.0]non-1⁽⁹⁾-en-8-one(1058705-71-7)

Safety Data

• Hazardous Substances Data: 1058705-71-7(Hazardous Substances Data)

Upstream product

• 1058705-44-4 (S)-1-cyclohex-1-en-1-yl-2-(dibenzylamino)-3-phenylpropan-1-one 
• 678150-52-2 (Z)-3-phenyl-1-propenyl N,n-diisopropylcarbamate 

Relevant articles and documents

Asymmetric synthesis of 3,4-annulated cyclopentenones from cycloalkenyl ketones and vinyl carbamates by diastereoselective carbonyl addition/conrotatory 4π ring closure

1-Lithiated O-vinyl carbamates add with high induced diastereoselectivity onto enantiomerically pure cycloalk-1-enyl (1-dibenzylamino)alkyl ketones. Subsequent O-carbamoyl migration, followed by a torquoselective, antarafacial 4π ring closure, leads to ho