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Reaction of 3-Oxa-2-oxobicyclo[4.2.0]oct-4-ene-1-carboxylate with Dimethylsulfoxonium Methylide.
Hsieh, Yun-Han; Iwasaki, Hiroki; Iwai, Yumina; Tanabe, Yuki; Taketomo, Rinako; Yamanishi, Suzuna; Tanaka, Yuichiro; Kojima, Naoto; Yamashita, Masayuki.
Afiliação
  • Hsieh YH; Kyoto Pharmaceutical University.
  • Iwasaki H; Kyoto Pharmaceutical University.
  • Iwai Y; Kyoto Pharmaceutical University.
  • Tanabe Y; Kyoto Pharmaceutical University.
  • Taketomo R; Kyoto Pharmaceutical University.
  • Yamanishi S; Kyoto Pharmaceutical University.
  • Tanaka Y; Kyoto Pharmaceutical University.
  • Kojima N; Kyoto Pharmaceutical University.
  • Yamashita M; Kyoto Pharmaceutical University.
Chem Pharm Bull (Tokyo) ; 69(4): 391-399, 2021.
Article em En | MEDLINE | ID: mdl-33790083
We have been interested in the reactivities of small-ring compounds and have reported reactions that proceed through cyclopropane intermediates starting from coumarin derivatives bearing an electron-withdrawing group at the 3-position or 2-oxo-2H-pyran-3-carboxylate derivatives and dimethylsulfoxonium methylide. This time, the reaction between 3-oxa-2-oxobicyclo[4.2.0]oct-4-ene-1-carboxylate and dimethylsulfoxonium methylide has been investigated. 3a,4,5,7a-Tetrahydro-7-hydroxybenzofuran-6-carboxylate and/or 2-hydroxybicyclo[4.1.0]hept-2-ene-3-carboxylate were obtained. The compounds were characterized using various spectral and X-ray crystallographic techniques. A plausible reaction mechanism has been discussed. This reaction was applied to some 3-oxa-2-oxobicyclo[4.2.0]oct-4-ene-1-carboxylate derivatives to clarify the generality.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Compostos de Sulfônio / Compostos Bicíclicos com Pontes / Ácidos Carboxílicos Idioma: En Revista: Chem Pharm Bull (Tokyo) Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Compostos de Sulfônio / Compostos Bicíclicos com Pontes / Ácidos Carboxílicos Idioma: En Revista: Chem Pharm Bull (Tokyo) Ano de publicação: 2021 Tipo de documento: Article