145471-64-3

Basic information

• Product Name: 4-oxo-3-(phenylsulfonyl)-12-(p-toluenesulfonyl)-1,4,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine
• Synonyms: 4-oxo-3-(phenylsulfonyl)-12-(p-toluenesulfonyl)-1,4,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine
• CAS NO: 145471-64-3
• Molecular Weight: 532.641
• Mol File: 145471-64-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-oxo-3-(phenylsulfonyl)-12-(p-toluenesulfonyl)-1,4,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-oxo-3-(phenylsulfonyl)-12-(p-toluenesulfonyl)-1,4,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine(145471-64-3)
• EPA Substance Registry System: 4-oxo-3-(phenylsulfonyl)-12-(p-toluenesulfonyl)-1,4,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine(145471-64-3)

Safety Data

• Hazardous Substances Data: 145471-64-3(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 4942-85-2 1,2,3,4,6,7,12,12b-octahydroindolo<2,3-a>quinolizine-4-one 
• 882-33-7 diphenyldisulfane 
• 145471-62-1 4-oxo-3,3-bis(phenylthio)-12-(p-toluenesulfonyl)-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine 
• 145471-63-2 4-oxo-3-(phenylsulfinyl)-12-(p-toluenesulfonyl)-1,4,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine 

Downstream Products

• 145471-67-6 C₂₈H₃₀N₂O₅S 
• 145471-66-5 C₃₄H₃₄N₂O₇S₂ 
• 483-29-4 (+/-)-3-epi-allo-yohimbone 
• 145471-65-4 (4aR,13bS,14aR)-4a-Benzenesulfonyl-13-(toluene-4-sulfonyl)-4,4a,7,8,13,13b,14,14a-octahydro-1H,3H-indolo[2',3':3,4]pyrido[1,2-b]isoquinoline-2,5-dione 
• 145471-65-4 (4aR,13bR,14aR)-4a-Benzenesulfonyl-13-(toluene-4-sulfonyl)-4,4a,7,8,13,13b,14,14a-octahydro-1H,3H-indolo[2',3':3,4]pyrido[1,2-b]isoquinoline-2,5-dione 

Relevant articles and documents

Stereocontrolled Annulations of Indolo[2,3-a]quinolizidine-Derived Lactams with a Silylated Nazarov Reagent: Access to Allo and Epiallo Yohimbine-Type Derivatives

The facial selectivity of double Michael addition reactions of the silylated Nazarov reagent 4 to unsaturated indolo[2,3-a]quinolizidine lactams 3 has been studied. Pentacyclic 3-H/15-H trans adducts 5 are generated from Nind-unsubstituted lact