Your browser doesn't support javascript.
loading
Synthesis of 2,2-Dialkyl Chromanes by Intramolecular Ullmann C-O Coupling Reactions toward the Total Synthesis of D-α-Tocopherol.
Tsubogo, Tetsu; Aoyama, Saki; Takeda, Rika; Uchiro, Hiromi.
Afiliação
  • Tsubogo T; Faculty of Pharmaceutical Sciences, Tokyo University of Science.
  • Aoyama S; Division of Fusion of Regenerative Medicine with DDS, Research Institute for Science and Technology (RIST), Tokyo University of Science.
  • Takeda R; Faculty of Pharmaceutical Sciences, Tokyo University of Science.
  • Uchiro H; Faculty of Pharmaceutical Sciences, Tokyo University of Science.
Chem Pharm Bull (Tokyo) ; 66(9): 843-846, 2018.
Article em En | MEDLINE | ID: mdl-30175739
ABSTRACT
The complete synthesis of D-α-tocopherol was achieved using our developed-Ullmann C-O coupling reaction as a key reaction. The synthesis of the core structure of D-α-tocopherol, which is a chiral chromane, has never been reported using intramolecular Ullmann C-O coupling reactions owing to the low reactivity of electron-rich iodoarenes with tertiary alcohols. Because the developed intramolecular C-O coupling reactions prefer electron-rich iodoarenes with tertiary alcohols, we successfully synthesized the chiral chromane core and achieved the total synthesis of D-α-tocopherol.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromanos / Alfa-Tocoferol Idioma: En Revista: Chem Pharm Bull (Tokyo) Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromanos / Alfa-Tocoferol Idioma: En Revista: Chem Pharm Bull (Tokyo) Ano de publicação: 2018 Tipo de documento: Article