447408-34-6

Basic information

• Product Name: 8a-allyl-4-(tert-butyl-diphenyl-silanyloxy)-2-(toluene-4-sulfonyl)-3,4,4a,8a-tetrahydro-2H,5H-isoquinoline-1,6-dione
• Synonyms: 8a-allyl-4-(tert-butyl-diphenyl-silanyloxy)-2-(toluene-4-sulfonyl)-3,4,4a,8a-tetrahydro-2H,5H-isoquinoline-1,6-dione
• CAS NO: 447408-34-6
• Molecular Weight: 613.85
• Mol File: 447408-34-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 8a-allyl-4-(tert-butyl-diphenyl-silanyloxy)-2-(toluene-4-sulfonyl)-3,4,4a,8a-tetrahydro-2H,5H-isoquinoline-1,6-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 8a-allyl-4-(tert-butyl-diphenyl-silanyloxy)-2-(toluene-4-sulfonyl)-3,4,4a,8a-tetrahydro-2H,5H-isoquinoline-1,6-dione(447408-34-6)
• EPA Substance Registry System: 8a-allyl-4-(tert-butyl-diphenyl-silanyloxy)-2-(toluene-4-sulfonyl)-3,4,4a,8a-tetrahydro-2H,5H-isoquinoline-1,6-dione(447408-34-6)

Safety Data

• Hazardous Substances Data: 447408-34-6(Hazardous Substances Data)

Upstream product

• 447408-46-0 5-(tert-butyl-diphenyl-silanyloxy)-3-phenylselanyl-1-(toluene-4-sulfonyl)-piperidin-2-one 
• 447408-30-2 3-allyl-5-(tert-butyl-diphenyl-silanyloxy)-1-(toluene-4-sulfonyl)-5,6-dihydro-1H-pyridin-2-one 
• 447408-47-1 5-(tert-butyl-diphenyl-silanyloxy)-3-iodo-1-(toluene-4-sulfonyl)-5,6-dihydro-1H-pyridin-2-one 
• 447408-27-7 5-(tert-butyl-diphenyl-silanyloxy)-1-(toluene-4-sulfonyl)-piperidin-2-one 
• 447408-28-8 5-(tert-butyl-diphenyl-silanyloxy)-1-(toluene-4-sulfonyl)-5,6-dihydro-1H-pyridin-2-one 
• 102774-92-5 (R)-(+)-5-Hydroxy-2-oxopiperidine 
• 447408-45-9 5-tert-Butyldimethylsiloxy-2-piperidone 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 98-59-9 p-toluenesulfonyl chloride 

Relevant articles and documents

Evaluation of diene hierarchies for Diels-Alder reactions en route to xestocyclamine A: Elaboration of an ansa bridge by B-alkyl Suzuki macrocyclization

A double Michael addition of amine 2 to 1 was a key reaction in the synthesis of the isoquinuclidine core 4 of xestocyclamine A, a protein kinase C inhibitor. The first ansa bridge was formed efficiently by a B-alkyl Suzuki coupling in 3. TBDPS = tert-but