trans-acetonide controlled endo-selective intramolecular nitrone-alkene cycloaddition of hept-6-enoses: A facile entry to calystegines, tropanes, and hydroxylated aminocycloheptanes

Tony K.M. Shing, Wai F. Wong, Taketo Ikeno, Tohru Yamada

研究成果: Article査読

41 被引用数 (Scopus)

抄録

(Chemical Equation Presented) High-yielding endo-selective intramolecular nitrone-alkene cycloaddition (INAC) reactions of hept-6-enoses controlled by a trans-acetonide to give bridged bicyclo[4.2.1]isoxazolidines exclusively are realized for the first time. The cycloadducts were readily transformed into calystegine, tropane, and hydroxylated aminocycloheptane frameworks.

本文言語English
ページ(範囲)207-209
ページ数3
ジャーナルOrganic Letters
9
2
DOI
出版ステータスPublished - 2007 1 18

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

フィンガープリント 「trans-acetonide controlled endo-selective intramolecular nitrone-alkene cycloaddition of hept-6-enoses: A facile entry to calystegines, tropanes, and hydroxylated aminocycloheptanes」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

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