262847-01-8

Basic information

• Product Name: 3-Furancarboxylic acid, 4-[3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]propyl]-4-ethyltetrahydro-2-oxo -, methyl ester, (4S)-
• CAS NO: 262847-01-8
• Molecular Formula: C27H36O5Si
• Molecular Weight: 468.665
• Mol File: 262847-01-8.mol

Chemical Properties

• CAS DataBase Reference: 3-Furancarboxylic acid, 4-[3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]propyl]-4-ethyltetrahydro-2-oxo -, methyl ester, (4S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Furancarboxylic acid, 4-[3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]propyl]-4-ethyltetrahydro-2-oxo -, methyl ester, (4S)-(262847-01-8)
• EPA Substance Registry System: 3-Furancarboxylic acid, 4-[3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]propyl]-4-ethyltetrahydro-2-oxo -, methyl ester, (4S)-(262847-01-8)

Safety Data

• Hazardous Substances Data: 262847-01-8(Hazardous Substances Data)

Upstream product

• 262846-97-9 (2S)-[5-(tert-butyldiphenylsilyloxy)-2-ethylpentyl]-α-diazo-α-(methoxycarbonyl)acetate 
• 262847-00-7 (2S)-[5-(t-butyldiphenylsilyloxy)-2-ethylpentyl]-α-(methoxycarbonyl)acetate 
• 393563-12-7 (2S)-(2-ethyl-5-hydroxypentyl)-α-(methoxycarbonyl)acetate 
• 393563-11-6 methyl (S)-(2-ethyl-4-pentenyl)malonate 
• 121074-21-3 (2S)-2-ethyl-4-penten-1-ol 
• 96930-18-6 (4R,5S)-4-methyl-3-pent-4-enoyl-5-phenyloxazolidin-2-one 
• 393563-10-5 (S)-2-ethylpent-4-enoic acid 
• 393563-09-2 (4R,5S)-3-[(2R)-2((1R*)-1-(phenoxythiocarbonyloxy)ethyl)-1-oxo-4-pentenyl]-4-methyl-5-phenyl-2-oxazolidinone 
• 393563-08-1 (4R,5S)-3[(2R)-2-((1R*)-1-hydroxyethyl)-1-oxo-4-pentenyl]-4-methyl-5-phenyl-2-oxazolidinone 
• 121074-25-7 (4R,5S)-3-[(2S)-1-oxo-2-ethyl-4-pentenyl]-4-methyl-5-phenyl-2-oxazolidinone 

Downstream Products

• 262847-09-6 (4S)-4-[3-(tert-butyldiphenylsilyloxypropyl)]-4-ethyldihydro-2(3H)-furanone 
• 393563-22-9 (1S,12bR)-1-ethyl-1-(2-tert-butyldiphenylsilyloxyethyl)-4-oxo-2,3,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizine 
• 393563-18-3 (1S,12bS)-1-ethyl-1-(2-tert-butyldiphenylsilyloxyethyl)-4-oxo-2,3,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizine 
• 262847-04-1 (5S)-N-[2-(3-indolyl)ethyl]-5-ethyl-5-(2-tert-butyldiphenylsiloxyethyl)-6-hydroxy-δ-lactam 
• 262847-03-0 (4S)-N-[2-(3-indolyl)-ethyl]-4-ethyl-4-hydroxymethyl-6-tert-butyldiphenylsiloxyhexamide 
• 393563-17-2 (4S)-N-[2-(3-indolyl)ethyl]-4-ethyl-4-(2-tert-butyldiphenylsiloxyethyl)-5-oxopentamide 
• 4880-88-0 vinburnine 

Relevant articles and documents

Asymmetric synthesis of (-)-eburnamonine and (+)-epi-eburnamonine from (4s)-4-ethyl-4-[2-(hydroxycarbonyl)ethyl]-2-butyrolactone

The key chiral nonracemic 4,4-disubstituted 2-butyrolactone carboxylic acid, (S)-4, is readily accessible via an efficient and stereospecific dirhodium(II) tetraacetate catalyzed tertiary C-H insertion reaction of the diazomalonate (S)-5. The coupling of the acid (S)-4 with tryptamine produces the amide (S)-3, which is then transformed into the aldehyde 23 and hydroxy-lactam 24. Acid-mediated Pictet-Spengler cyclization of 23 and 24 produces the tetracyclic indole lactams (1S,-12bS)-25a and (1S,12bR)-25b. Compounds 25a and 25b are converted, via the lactam alcohols 30a and 30b, to (-)-eburnamonine (1a) and (+)-epi-eburnamonine (1b).

Total synthesis of (-)-eburnamonine and (+)-epi-eburnamonine from a chiral non-racemic 4,4-disubstituted γ-lactone

The total synthesis of (-)-eburnamonine and (+)-epi-eburnamonine was successfully achieved using a key chiral non-racemic 4,4-disubstituted γ- lactone 4 that was prepared via the Rh(II) carbenoid mediated tertiary C-H insertion reaction of a chiral non-racemic diazomalonate 5. (C) 2000 Elsevier Science Ltd.