Stockmann, Vegar published the artcileStudies on reactive pyridylketones formed by Weinreb transformations, Application of N-Methoxy-N-methylisonicotinamide, the publication is Journal of Heterocyclic Chemistry (2012), 49(3), 613-620, database is CAplus.
A method was developed to allow the preparation of reactive pure vinyl pyridyl ketones and activated vinyl ketones, in general, to be used in further reactions, such as cycloadditions The process is based on the Weinreb’s amide transformation and includes a quaternary ammonium intermediate and subsequent elimination. Addnl., based on the authors’ previous results on the malonate alkylation of 3-nitropyridines and subsequent synthetic applications, they present studies on the transformation of Me 4-(methoxycarbonyl)-3-pyridineacetate via the corresponding Weinreb amide and reactive methylpyridyl- and allyl pyridyl ketones into isoquinoline derivatives
Journal of Heterocyclic Chemistry published new progress about 100377-32-0. 100377-32-0 belongs to amides-buliding-blocks, auxiliary class Pyridine,Amine,Amide, name is N-Methoxy-N-methylisonicotinamide, and the molecular formula is C6H3ClFNO2, Application of N-Methoxy-N-methylisonicotinamide.
Referemce:
https://en.wikipedia.org/wiki/Amide,
Amide – an overview | ScienceDirect Topics