42510-59-8

Basic information

• Product Name: 1-phenylhexahydro-3H-oxazolo[3,4-a]pyridin-3-one
• CAS NO: 42510-59-8
• Molecular Weight: 217.268
• Mol File: 42510-59-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-phenylhexahydro-3H-oxazolo[3,4-a]pyridin-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenylhexahydro-3H-oxazolo[3,4-a]pyridin-3-one(42510-59-8)
• EPA Substance Registry System: 1-phenylhexahydro-3H-oxazolo[3,4-a]pyridin-3-one(42510-59-8)

Safety Data

• Hazardous Substances Data: 42510-59-8(Hazardous Substances Data)

Upstream product

• 120153-69-7 2-Benzoyl-piperidine-1-carboxylic acid phenyl ester 
• 30964-00-2 hept-6-ynoic acid 
• 151978-58-4 tert-butyl hex-5-yn-1-ylcarbamate 
• 729553-31-5 (1-Benzyl-piperidin-2-yl)-phenyl-methanone 
• 75844-69-8 t-butyl piperidinecarboxylate 
• 120153-68-6 N-benzylpiperidine-2-carbonitrile 
• 100-52-7 benzaldehyde 

Downstream Products

• 5583-31-3 threo-α-phenyl-2-piperidinemethanol 

Relevant articles and documents

Photocatalytic Oxyamination of Alkenes: Copper(II) Salts as Terminal Oxidants in Photoredox Catalysis

A photocatalytic method for the oxyamination of alkenes using simple nucleophilic nitrogen atom sources in place of prefunctionalized electrophilic nitrogen atom donors is reported. Copper(II) is an inexpensive, practical, and uniquely effective terminal oxidant for this process. In contrast to oxygen, peroxides, and similar oxidants commonly utilized in non-photochemical oxidative methods, the use of copper(II) as a terminal oxidant in photoredox reactions avoids the formation of reactive heteroatom-centered radical intermediates that can be incompatible with electron-rich functional groups. As a demonstration of the generality of this concept, it has been shown that diamination and deoxygenation reactions can also be accomplished using similar photooxidative conditions.

A NEW AND DIASTEREOSELECTIVE SYNTHESIS OF THREO-ARYL-2-PIPERIDYLMETHANOL DERIVATIVES

A diastereoselective synthesis of threo-aryl-2-piperidyl- and aryl-1,2,3,6-tetrahydro-2-pyridylmethanol derivatives is described.The stereochemestry is controlled by intramolecularly assisted NaBH4 reduction of the intermediate carbamates 3.