Unprecedented nucleophile-promoted 1,7-S or Se shift reactions under Pummerer reaction conditions of 4-alkenyl-3-sulfinylmethylpyrroles.

Go, Takashi; Morimatsu, Akane; Wasada, Hiroaki; Tanabe, Genzoh; Muraoka, Osamu; Sawada, Yoshiharu; Yoshimatsu, Mitsuhiro

Go, Takashi; Morimatsu, Akane; Wasada, Hiroaki; Tanabe, Genzoh; Muraoka, Osamu; Sawada, Yoshiharu; Yoshimatsu, Mitsuhiro.

Afiliación

Go T; Department of Chemistry, Faculty of Education, Gifu University, Yanagido 1-1, Gifu 501-1193, Japan.
Morimatsu A; Department of Chemistry, Faculty of Education, Gifu University, Yanagido 1-1, Gifu 501-1193, Japan.
Wasada H; Department of Chemistry, Faculty of Regional Study, Gifu University, Yanagido 1-1, Gifu 501-1193, Japan.
Tanabe G; School of Pharmacy, Kindai University, 3-4-1 Kowakae, Higashi-osaka, Osaka 577-8502, Japan.
Muraoka O; School of Pharmacy, Kindai University, 3-4-1 Kowakae, Higashi-osaka, Osaka 577-8502, Japan.
Sawada Y; Life Science Research Center, Gifu University, Yanagido 1-1, Gifu 501-1193, Japan.
Yoshimatsu M; Department of Chemistry, Faculty of Education, Gifu University, Yanagido 1-1, Gifu 501-1193, Japan.

Beilstein J Org Chem ; 14: 2722-2729, 2018.

Article en En | MEDLINE | ID: mdl-30498522

Palabras clave

1,7-sulfur shift; Pummerer reaction; hydroamination; pyrrole; pyrroloazepine

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Beilstein J Org Chem Año: 2018 Tipo del documento: Article País de afiliación: Japón

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