Literature DB >> 30475518

The Use of the Comins-Meyers Amide in Synthetic Chemistry: an Overview.

Serena Monticelli, Giovanna Parisi, Marta Rui, Karen de la Vega-Hernández, Irene Murgia, Raffaele Senatore, Wolfgang Holzer, Ernst Urban, Thierry Langer, Vittorio Pace.   

Abstract

Formylation reactions are fundamental operations in synthetic chemistry allowing the incorporation into a given structure formyl groups amenable to further deiivatization. Conceptually, the introduction of such groups through the reaction between an electrophilic donor and a nucleophilic acceptor (i.e. organometallic reagent) constitutes a reliable technique with widespread applications. In this Highlight, we summarize the effectiveness of the so called Comnins-Meyers amide - [2-(N-methyl-N-formylamino]pyridine - in such a chemistry with vistas to the synthesis of natural products and biologically active substrates.

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Year:  2016        PMID: 30475518

Source DB:  PubMed          Journal:  Nat Prod Commun        ISSN: 1555-9475            Impact factor:   0.986


  1 in total

1.  Synthesis of MAPA Reagents and 2-Alkyl(aryl)aminopyridines from 2-Bromopyridine Using the Goldberg Reaction.

Authors:  Daniel L Comins
Journal:  Molecules       Date:  2022-03-11       Impact factor: 4.411

  1 in total

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