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1.
J Org Chem ; 89(1): 784-792, 2024 Jan 05.
Artigo em Inglês | MEDLINE | ID: mdl-38096498

RESUMO

A novel methodology for the synthesis of indanone derivates has been developed. The palladium-catalyzed annulation reaction of o-bromobenzaldehydes with norbornene derivatives is achieved through extremely concise reaction processes. The indanone skeleton was established directly via C-H activation of the aldehyde group under a mild reaction condition. This method is simple and practical, which simplified the traditional synthesis method for the rapid construction of indanone.

2.
J Org Chem ; 89(14): 9841-9852, 2024 Jul 19.
Artigo em Inglês | MEDLINE | ID: mdl-38917372

RESUMO

A novel methodology for the synthesis of nitrones via palladium-catalyzed redox cross-coupling of nitro compounds and alcohols is established. The protocol is a mild, convenient, ligand-free, and scalable synthesis method that can be compatible with various nitro compounds and alcohols. Nitrone is a significant multifunctional platform synthon which can be synthesized directly and efficiently via this tactic from commercially available and cheap raw materials.

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