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Showing papers on "Benzopyrans published in 2023"



Journal ArticleDOI
TL;DR: In this paper , a new functionalized magnetic nanocatalyst was designed through the reaction between 2-aminomethylpyridine (AMP) and Fe3O4@SiO2@propyl.

Journal ArticleDOI
TL;DR: In this paper , a Pd-catalyzed denitrative intramolecular Mizoroki-Heck reaction of nitroarenes bearing an alkene was developed.
Abstract: A Pd-catalyzed denitrative intramolecular Mizoroki–Heck reaction of nitroarenes with alkenes was developed. Pd/BrettPhos is an effective catalyst for this transformation, producing 5- and 6-membered cyclic products such as indenes and benzopyrans. Since a tethered-alkene group can be introduced onto the nitroarene core through nucleophilic aromatic substitution (SNAr), the present denitrative reaction would provide a convergent synthetic method for benzo-fused cyclic compounds. A Pd-catalyzed denitrative intramolecular Mizoroki–Heck reaction of nitroarenes bearing an alkene was developed. Pd/Brettphos is an effective catalyst, producing 5- and 6-membered cyclic products such as indenes and benzopyrans. Since a tethered-alkene group can be introduced onto the nitroarene core through nucleophilic aromatic substitution (SNAr), the present denitrative reaction would provide a convergent synthetic method of benzo-fused cyclic compounds.

Journal ArticleDOI

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TL;DR: In this article , a new functionalized magnetic nanocatalyst was designed through the reaction between 2-aminomethylpyridine (AMP) and Fe3O4@SiO2@propyl.