Highly stereoselective Lewis acid mediated conjugate radical additions to methyl α-D-glucopyranoside derivatives tethering an unsaturated ester moiety at C-4

Ryosuke Munakata, Kiichiro Totani, Ken Ichi Takao, Kin Ichi Tadano

研究成果: Article査読

22 被引用数 (Scopus)

抄録

The Lewis acid mediated conjugate additions of alkyl radicals to some 4- crotonyl derivatives of methyl α-D-glucopyranoside proceeded with a high level of diastereochemical induction to provide the adducts carrying a β- chiral butanoic ester.

本文言語English
ページ(範囲)979-982
ページ数4
ジャーナルSynlett
7
出版ステータスPublished - 2000 8月 9

ASJC Scopus subject areas

  • 有機化学

フィンガープリント

「Highly stereoselective Lewis acid mediated conjugate radical additions to methyl α-D-glucopyranoside derivatives tethering an unsaturated ester moiety at C-4」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。

引用スタイル