1414851-96-9

Basic information

• Product Name: diphenyl (3R,4R)-1-(benzyloxycarbonyl)-4-(4-methoxypicolinamido)pyrrolidin-3-ylphosphonate
• Synonyms: diphenyl (3R,4R)-1-(benzyloxycarbonyl)-4-(4-methoxypicolinamido)pyrrolidin-3-ylphosphonate
• CAS NO: 1414851-96-9
• Molecular Weight: 587.569
• Mol File: 1414851-96-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: diphenyl (3R,4R)-1-(benzyloxycarbonyl)-4-(4-methoxypicolinamido)pyrrolidin-3-ylphosphonate(CAS DataBase Reference)
• NIST Chemistry Reference: diphenyl (3R,4R)-1-(benzyloxycarbonyl)-4-(4-methoxypicolinamido)pyrrolidin-3-ylphosphonate(1414851-96-9)
• EPA Substance Registry System: diphenyl (3R,4R)-1-(benzyloxycarbonyl)-4-(4-methoxypicolinamido)pyrrolidin-3-ylphosphonate(1414851-96-9)

Safety Data

• Hazardous Substances Data: 1414851-96-9(Hazardous Substances Data)

Upstream product

• 1124-33-0 4-nitraminopyridine N-oxide 
• 29082-91-5 4-methoxypyridine-2-carboxylic acid 
• 4712-55-4 diphenyl hydrogen phosphite 
• 1414851-50-5 3-carbobenzyloxy-6-(4-methoxypicolinoyl)-3,6-diazabicyclo[3.1.0]hexane 
• 19235-88-2 2-cyano-4-nitro-pyridine 

Relevant articles and documents

Cinchona alkaloid amides/dialkylzinc catalyzed enantioselective desymmetrization of aziridines with phosphites

The first highly enantioselective desymmetrization of aziridines with phosphites has been developed. Excellent yields and enantioselectivities were observed for the reaction with various aziridines using a new class of readily accessible chiral catalysts derived from 9-amino-9-deoxy-epi-cinchona alkaloids. In studies probing the reaction mechanism, we observed some complexes for the cinchona alkaloid amide-Zn(II) by ESI-MS analysis.