1617519-65-9

Basic information

• Product Name: (2S,3S)-2-(2-((tert-butyldimethylsilyl)oxy)ethyl)-N-methoxy-N-methyl-4-oxo-1-tritylazetidine-3-carboxamide
• Synonyms: (2S,3S)-2-(2-((tert-butyldimethylsilyl)oxy)ethyl)-N-methoxy-N-methyl-4-oxo-1-tritylazetidine-3-carboxamide
• CAS NO: 1617519-65-9
• Molecular Weight: 558.793
• Mol File: 1617519-65-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2S,3S)-2-(2-((tert-butyldimethylsilyl)oxy)ethyl)-N-methoxy-N-methyl-4-oxo-1-tritylazetidine-3-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S)-2-(2-((tert-butyldimethylsilyl)oxy)ethyl)-N-methoxy-N-methyl-4-oxo-1-tritylazetidine-3-carboxamide(1617519-65-9)
• EPA Substance Registry System: (2S,3S)-2-(2-((tert-butyldimethylsilyl)oxy)ethyl)-N-methoxy-N-methyl-4-oxo-1-tritylazetidine-3-carboxamide(1617519-65-9)

Safety Data

• Hazardous Substances Data: 1617519-65-9(Hazardous Substances Data)

Upstream product

• 1617519-64-8 (S)-6-((tert-butyldimethylsilyl)oxy)-2-diazo-N-methoxy-N-methyl-3-oxo-4-(tritylamino)hexanamide 
• 1617519-63-7 (S)-6-((tert-butyldimethylsilyl)oxy)-N-methoxy-N-methyl-3-oxo-4-(tritylamino)hexanamide 
• 1617519-62-6 2-((3S)-2-hydroxy-3-(tritylamino)tetrahydrofuran-2-yl)-N-methoxy-N-methylacetamide 
• 83427-81-0 (S)-N-tritylhomoserine lactone 

Downstream Products

• 1617519-61-5 (2S,3S)-2-(2-hydroxyethyl)-N-methoxy-N-methyl-4-oxo-1-tritylazetidine-3-carboxamide 
• 1617519-66-0 2-((2S,3S)-3-(methoxy(methyl)carbamoyl)-4-oxo-1-tritylazetidin-2-yl)acetic acid 
• 1617519-67-1 (2S,3S)-2-(2-(benzylamino)-2-oxoethyl)-N-methoxy-N-methyl-4-oxo-1-tritylazetidine-3-carboxamide 
• 1617519-60-4 (1R,5S)-2-benzyl-N-methoxy-N-methyl-3,7-dioxo-6-trityl-2,6-diazabicyclo[3.2.0]heptane-1-carboxamide 

Relevant articles and documents

Preparation of fused β-lactams through Weinreb amide α-anions

Enantiomerically pure β-lactams bearing a Weinreb amide functionality at the C3 position have been shown to be excellent substrates for α-alkylation reactions, generating C3 quaternary centers with predictable absolute stereochemistry. In addition, oxidative coupling of C3/C4 dianions affords entry to fused β,γ-bislactam systems.