184867-89-8

Basic information

• Product Name: (S)-1-Furan-2-yl-3-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-2-(4-methyl-pent-4-enyl)-propane-1,3-dione
• CAS NO: 184867-89-8
• Molecular Weight: 395.455
• Mol File: 184867-89-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-1-Furan-2-yl-3-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-2-(4-methyl-pent-4-enyl)-propane-1,3-dione(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-Furan-2-yl-3-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-2-(4-methyl-pent-4-enyl)-propane-1,3-dione(184867-89-8)
• EPA Substance Registry System: (S)-1-Furan-2-yl-3-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-2-(4-methyl-pent-4-enyl)-propane-1,3-dione(184867-89-8)

Safety Data

• Hazardous Substances Data: 184867-89-8(Hazardous Substances Data)

Upstream product

• 39764-81-3 6-methyl-6-heptenoic acid chloride 
• 166533-72-8 ethyl 6-methyl-6-heptenoate 
• 5212-67-9 6-methyl-hept-6-enoic acid 
• 527-69-5 2-furancarbonyl chloride 
• 184867-88-7 (+)-N-(1-oxo-6-methylhept-6-ene)-2-methyl-3-phenyl-4-oxazolidin-5-one 

Downstream Products

• 184867-90-1 (R)-1-Furan-2-yl-6-methyl-2-trityloxymethyl-hept-6-en-1-ol 

Relevant articles and documents

New strategy for the synthesis of the taxane diterpenes: Formation of the BC-rings of taxol via a [5+2]-pyrylium ylide-alkene cyclization, ring expansion strategy

The BC-rings of taxol can be synthesized using an intramolecular [5+2]- pyrylium ylide-alkene cyclization, followed by gem-methylcyclopropanation and reductive cleavage of the internal cyclopropane bond.