Cargando…

2,5-[C(4)+C(2)] Ringtransformation of Pyrylium Salts with α-Sulfinylacetaldehydes

A rapid synthesis of chiral sulfoxide-functionalized meta-terphenyl derivatives by a 2,5-[C(4)+C(2)] ring transformation reaction of pyrylium salts with in situ generated enantiomerically pure α-sulfinylacetaldehydes is described in this paper. This synthetic method demonstrates, for the first time,...

Descripción completa

Detalles Bibliográficos
Autores principales: Bauer, Dominik, Hofmann, Kathrin, Reggelin, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673159/
https://www.ncbi.nlm.nih.gov/pubmed/38005312
http://dx.doi.org/10.3390/molecules28227590
Descripción
Sumario:A rapid synthesis of chiral sulfoxide-functionalized meta-terphenyl derivatives by a 2,5-[C(4)+C(2)] ring transformation reaction of pyrylium salts with in situ generated enantiomerically pure α-sulfinylacetaldehydes is described in this paper. This synthetic method demonstrates, for the first time, the use of α-sulfinylacetaldehydes in a reaction sequence initiated by the nucleophilic attack of pyrylium salts by α-sulfinylcarbanions to generate chiral aromatic systems. The method presented shows a broad applicability starting with various methyl sulfoxides and a number of functionalized pyrylium salts, furnishing meta-terphenyls with complex substitution patterns from readily accessible starting compounds.