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Enantioselective Total Syntheses of Preussomerins: Control of Spiroacetal Stereogenicity by Photochemical Reaction of a Naphthoquinone through 1,6‐Hydrogen Atom Transfer

We report the enantioselective total syntheses of preussomerins EG(1), EG(2), and EG(3). The key transformation is a stereospecific photochemical reaction involving 1,6‐hydrogen atom transfer to achieve retentive replacement of a C−H with a C−O bond, enabling otherwise‐difficult control of the spiro...

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Detalles Bibliográficos
Autores principales:	Ando, Yoshio, Ogawa, Daichi, Ohmori, Ken, Suzuki, Keisuke
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Research Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107447/ https://www.ncbi.nlm.nih.gov/pubmed/36446739 http://dx.doi.org/10.1002/anie.202213682

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