139259-03-3

Basic information

• Product Name: N-<(S)-2-carboxymethyl-2-(indol-3-yl)ethyl>-(6R)-2,3-didehydro-4-oxo-6- piperidine
• Synonyms: N-<(S)-2-carboxymethyl-2-(indol-3-yl)ethyl>-(6R)-2,3-didehydro-4-oxo-6- piperidine
• CAS NO: 139259-03-3
• Molecular Weight: 419.437
• Mol File: 139259-03-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-<(S)-2-carboxymethyl-2-(indol-3-yl)ethyl>-(6R)-2,3-didehydro-4-oxo-6- piperidine(CAS DataBase Reference)
• NIST Chemistry Reference: N-<(S)-2-carboxymethyl-2-(indol-3-yl)ethyl>-(6R)-2,3-didehydro-4-oxo-6- piperidine(139259-03-3)
• EPA Substance Registry System: N-<(S)-2-carboxymethyl-2-(indol-3-yl)ethyl>-(6R)-2,3-didehydro-4-oxo-6- piperidine(139259-03-3)

Safety Data

• Hazardous Substances Data: 139259-03-3(Hazardous Substances Data)

Upstream product

• 4299-70-1 L-tryptophan methyl ester 
• 555-16-8 4-nitrobenzaldehdye 
• 54125-02-9 danishefsky's diene 
• 177217-36-6 (S)-3-(1H-Indol-3-yl)-2-{[1-(4-nitro-phenyl)-meth-(E)-ylidene]-amino}-propionic acid methyl ester 

Downstream Products

• 139259-15-7 1,2,3,4,6,7,12,12b-octahydro-2-oxoindolo<2,3-a>-(4R,6S,12bR)-6-carboxymethyl-4- quinolizine 

Relevant articles and documents

Asymmetric Synthesis of Indoloquinolizidin-2-ones Congeners to Yohimbine-Type Alkaloids

Schiff bases derived from tryptophan methyl ester and tryptamine react with Danishefkys diene in the presence of ZnCl2 to give enaminones which are subsequently transformed into indoloquinolizidin-2-ones by acid-catalyzed cyclization.These tetracyc