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Marie Gizolme

Publications and source records attributed to Marie Gizolme.

2 recordsLinked to original sources

O-arylative Passerini reactions.

The three-component addition of isocyanides to phenol derivatives and aldehydes proceeds easily in methanol to form O-arylated compounds in a new Passerini-type reaction. The key step of the conversion lies in an irreversible Smiles rearrangement of intermediate phenoxyimidate adducts. It represents the first use of a Smiles rearrangement in a Passerini reaction. [reaction: see text]

Journal Article↗

Direct access to heterocyclic scaffolds by new multicomponent Ugi-Smiles couplings.

New heterocyclic scaffolds can be easily prepared by the coupling of heteroaromatic phenols (pyridines, pyrimidines) with carbonyl compounds, amines, and isocyanides. This transformation related to the Ugi reaction probably involves a Smiles rearrangement. The scope of this methodology is further extended by the successful use of heterocyclic thiols to form highly functionalized thioamides.

Journal Article↗