Highly stereoselective Diels-Alder reactions achieved on some hexopyranosidic templates

T. Nagatsuka, S. Yamaguchi, K. Totani, K. I. Takao, K. I. Tadano

研究成果: Article

18 引用 (Scopus)

抜粋

The Diels-Alder reactions of some carbohydrate derivatives, as chiral acrylic esters, with cyclopentadiene proceed highly diastereoselectively to provide the adducts carrying a norbornene carboxylate. By reductive removal of the carbohydrate templates from the adducts, both 2S and 2R-enriched 5-norbornene-2-methanol are obtained.

元の言語English
ページ(範囲)481-484
ページ数4
ジャーナルSynlett
発行部数4
出版物ステータスPublished - 2001 4 24

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ASJC Scopus subject areas

  • Organic Chemistry

これを引用

Nagatsuka, T., Yamaguchi, S., Totani, K., Takao, K. I., & Tadano, K. I. (2001). Highly stereoselective Diels-Alder reactions achieved on some hexopyranosidic templates. Synlett, (4), 481-484.