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Spirocarbocycle Synthesis from Chloromethylarenes via Transition-Metal-Catalyzed Allylative Dearomatization and Ring Closure Metathesis.
Hu, Yanzhao; Zhang, Sheng; Yu, Xiaoqiang; Feng, Xiujuan; Yamaguchi, Masahiko; Bao, Ming.
Afiliação
  • Hu Y; State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116024, China.
  • Zhang S; State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116024, China.
  • Yu X; State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116024, China.
  • Feng X; State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116024, China.
  • Yamaguchi M; State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116024, China.
  • Bao M; Department of Organic Chemistry, Graduate School of Pharmaceutical Science, Tohoku University, Sendai 980-8578, Japan.
J Org Chem ; 87(12): 8229-8236, 2022 06 17.
Article em En | MEDLINE | ID: mdl-35658456
A strategy for the synthesis of spirocarbocycles by using chloromethyl arenes as starting materials is described in this paper. The palladium-catalyzed allylative dearomatization and the subsequent ruthenium-catalyzed ring closure metathesis proceeded smoothly under mild conditions to produce the corresponding spirocarbocycle products with moderate to high yields. Benzene-ring-, naphthalene-ring-, and anthracene-ring-containing substrates can be easily transformed into spirocarbocycles by using the proposed method.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paládio / Rutênio Idioma: En Revista: J Org Chem Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paládio / Rutênio Idioma: En Revista: J Org Chem Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos