Name: 3-Pyridinecarboxaldehyde. Recently I am researching about FRIEDEL-CRAFTS REACTION; GENERATED IN-SITU; BETA-SUBSTITUTED TRYPTOPHANS; FORMED AZAOXYALLYL CATIONS; ENANTIOSELECTIVE SYNTHESIS; CYCLOADDITION REACTIONS; MICHAEL ADDITION; BISINDOLE ALKALOIDS; INDOLE; ALDEHYDES, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21672172]; project of Youth Science and Technology Innovation Team of Sichuan Province, China [2017TD0008]; Education Department of Sichuan Province [15CZ0016]. Published in GEORG THIEME VERLAG KG in STUTTGART ,Authors: Chen, Y; Guo, XQ; Zhou, C; Chen, LM; Kang, TR. The CAS is 500-22-1. Through research, I have a further understanding and discovery of 3-Pyridinecarboxaldehyde
A catalyst-free, base-mediated N- sec -alkylation of amides by reaction of sulfonylindoles and -halohydroxamates has been developed. The N- sec -alkylation of amides reaction is based on an intermolecular nucleophilic addition of vinylogous imine with N -(benzyloxy)meth-acrylamide/azaoxyallyl cations formed in situ and represents a simple way to give polyfunctionalized 3-indolyl methanamines in good to excellent yields.
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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem