921201-39-0

Basic information

• Product Name: tert-butyl (S)-1-(ethoxycarbonyl)-3-(benzyloxy)-3-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-enyl carbamate
• Synonyms: tert-butyl (S)-1-(ethoxycarbonyl)-3-(benzyloxy)-3-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-enyl carbamate
• CAS NO: 921201-39-0
• Molecular Weight: 435.518
• Mol File: 921201-39-0.mol

Chemical Properties

• CAS DataBase Reference: tert-butyl (S)-1-(ethoxycarbonyl)-3-(benzyloxy)-3-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-enyl carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (S)-1-(ethoxycarbonyl)-3-(benzyloxy)-3-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-enyl carbamate(921201-39-0)
• EPA Substance Registry System: tert-butyl (S)-1-(ethoxycarbonyl)-3-(benzyloxy)-3-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-enyl carbamate(921201-39-0)

Safety Data

• Hazardous Substances Data: 921201-39-0(Hazardous Substances Data)

Upstream product

• 100906-42-1 2-O-benzyl-3,4-O-isopropylidene-L-threose 

Downstream Products

• 921201-53-8 tert-butyl-(1R,3S,4S)-1-(ethoxycarbonyl)-3-(benzyloxy)-4-hydroxy-5-(tert-butyl dimethyl silyloxy)-pentyl carbamate 
• 921201-43-6 tert-butyl-(1S,3S,4S)-1-(ethoxycarbonyl)-3-(benzyloxy)-4-hydroxy-5-(tert-butyl dimethyl silyloxy)-pentyl carbamate 
• 921201-51-6 tert-butyl-(1R,3S,4S)-1-(ethoxycarbonyl)-3-(benzyloxy)-4,5-dihydroxy pentyl carbamate 
• 921201-41-4 tert-butyl-(1S,3S,4S)-1-(ethoxycarbonyl)-3-(benzyloxy)-4,5-dihydroxy pentyl carbamate 
• 921201-54-9 (2R,4S,5R)-ethyl-4-(benzyloxy)-5-(tert-butyl dimethyl silyloxy methyl)pyrrolidine-2-carboxylate 
• 921201-45-8 (2S,4S,5R)-ethyl-4-(benzyloxy)-5-(tert-butyl dimethyl silyloxy methyl)pyrrolidine-2-carboxylate 
• 921201-40-3 tert-butyl-(1S,3S)-1-(ethoxycarbonyl)-3-(benzyloxy)-3-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]propyl carbamate 
• 921201-50-5 tert-butyl-(1R,3S)-1-(ethoxycarbonyl)-3-(benzyloxy)-3-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]propyl carbamate 

Relevant articles and documents

Stereoselective synthesis of (-)-bulgecinine hydrochloride and its C-2 epimer from l-ascorbic acid

An efficient strategy for the stereocontrolled synthesis of (-)-bulgecinine hydrochloride 1 was accomplished by utilizing a Wittig Horner olefination, stereoselective reduction of the double bond and intramolecular N-alkylation to furnish the target.