| Literature DB >> 30475518 |
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.Entities:
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Year: 2016 PMID: 30475518
Source DB: PubMed Journal: Nat Prod Commun ISSN: 1555-9475 Impact factor: 0.986