288395-79-9

Basic information

• Product Name: C₃₀H₂₉NO₇
• Synonyms: C₃₀H₂₉NO₇
• CAS NO: 288395-79-9
• Molecular Weight: 515.563
• Mol File: 288395-79-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₀H₂₉NO₇(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₀H₂₉NO₇(288395-79-9)
• EPA Substance Registry System: C₃₀H₂₉NO₇(288395-79-9)

Safety Data

• Hazardous Substances Data: 288395-79-9(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 288395-76-6 C₂₉H₃₇NO₇Si 
• 288395-77-7 C₂₃H₂₃NO₇ 
• 288395-78-8 C₂₃H₂₁NO₇ 
• 288395-85-7 4-(1-Ethoxy-ethoxy)-benzo[1,3]dioxole-5-carboxylic acid [(1R,5S,6R)-5-(tert-butyl-dimethyl-silanyloxy)-7-oxa-bicyclo[4.1.0]hept-3-en-3-yl]-(4-methoxy-benzyl)-amide 
• 200182-34-9 C₂₈H₃₅NO₇Si 
• 200182-33-8 4-Hydroxy-benzo[1,3]dioxole-5-carboxylic acid [(1R,5S,6R)-5-(tert-butyl-dimethyl-silanyloxy)-7-oxa-bicyclo[4.1.0]hept-3-en-3-yl]-(4-methoxy-benzyl)-amide 
• 200182-32-7 4-(1-Ethoxy-ethoxy)-benzo[1,3]dioxole-5-carboxylic acid [(1R,5S,6R)-5-(tert-butyl-dimethyl-silanyloxy)-7-oxa-bicyclo[4.1.0]hept-3-en-3-yl]-amide 
• 288395-75-5 (+)-5-(tert-butyl-dimethylsilanyloxy)-7-oxa-bicyclo[4.1.0]hept-3-ene-3-carboxylic acid methyl ester 
• 200182-31-6 (+)-5-(tert-butyldimethylsilanyloxy)-7-oxa-bicyclo[4.1.0]hept-3-ene-3-carboxylic acid 
• 1028277-29-3 tert-Butyl-((1R,2S,6R)-4-isocyanato-7-oxa-bicyclo[4.1.0]hept-3-en-2-yloxy)-dimethyl-silane 
• 288395-83-5 5-butyryloxy-7-oxa-bicyclo[4.1.0]hept-3-ene-3-carboxylic acid methyl ester 
• 192210-65-4 5-bromo-4-(1-ethoxyethoxy)-2H-benzo[d]1,3-dioxolane 
• 106861-61-4 (+)-methyl (1β,2α,6β)-2-hydroxy-7-oxabicyclo<4,1,0>hept-3-ene-4-carboxylate 

Downstream Products

• 96203-70-2 pancratistatin 
• 288395-80-2 (1R,2R,4aS,11bR)-1-Benzyloxy-2-hydroxy-7-methoxy-5-(4-methoxy-benzyl)-1,4a,5,11b-tetrahydro-2H-[1,3]dioxolo[4,5-j]phenanthridin-6-one 
• 288395-81-3 (1R,2R,3S,4S,4aR,11bR)-1-benzyloxy-5-(4-methoxy-benzyl)-2,3,4-trihydroxy-7-methoxy-1,3,4,4a,5,11b-hexahydro-2H-[1,3]dioxolo[4,5-j]phenanthridin-6-one 

Relevant articles and documents

Studies on the narciclasine alkaloids: Total synthesis of (+)- narciclasine and (+)-pancratistatin

Enantioselective total syntheses of the antimmor alkaloids, (+)- narciclasine and (+)-pancratistatin, are reported. These syntheses feature a stereo- and regiocontrolled aryl enamide photocyclization to construct a common, advanced intermediate possessing a transfused BC substructure. Differential functional group interchange in the C-ring of this phenanthridone core structure allows for the production of the two target natural products in enantiomerically pure form.