Enantioselective Synthesis of (-)-10-Hydroxyacutuminine.

Grünenfelder, Denise C; Navarro, Raul; Wang, Haoxuan; Fastuca, Nicholas J; Butler, John R; Reisman, Sarah E

Grünenfelder, Denise C; Navarro, Raul; Wang, Haoxuan; Fastuca, Nicholas J; Butler, John R; Reisman, Sarah E.

Afiliação

Grünenfelder DC; The Warren and Katharine Schlinger Laboratory of Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Navarro R; The Warren and Katharine Schlinger Laboratory of Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Wang H; The Warren and Katharine Schlinger Laboratory of Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Fastuca NJ; The Warren and Katharine Schlinger Laboratory of Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Butler JR; The Warren and Katharine Schlinger Laboratory of Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Reisman SE; The Warren and Katharine Schlinger Laboratory of Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.

Angew Chem Int Ed Engl ; 61(16): e202117480, 2022 04 11.

Article em En | MEDLINE | ID: mdl-35112449

Assuntos

Ciclização; Reação de Cicloadição; Estereoisomerismo

Palavras-chave

Acutumine Alkaloids; Deoxychlorination; Dieckmann Cyclization; Total Synthesis; [2+2] Cycloaddition

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ciclização Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

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