Synthesis of both the enantiomers of lardolure, the aggregation pheromone of the acarid mite, lardoglyphus konoi

Kenji Mori, Shigefumi Kuwahara

研究成果: Article査読

47 被引用数 (Scopus)

抄録

Both the enantiomers of lardolure were synthesized in 100 % optical purity and 99.6 % diastereomeric purity by use of Fráter's diastereoselective alkylation as the key-step. Since (1R,3R,5R,7R)-enantiomer showed the same ORD sign and bioactivity as those shown by the natural pheromone, the structure of lardolure was established unambiguously as (1R,3R,5R,7R)-1,3,5,7-tetramethyldecyl formate.

本文言語English
ページ(範囲)5539-5544
ページ数6
ジャーナルTetrahedron
42
20
DOI
出版ステータスPublished - 1986
外部発表はい

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

フィンガープリント 「Synthesis of both the enantiomers of lardolure, the aggregation pheromone of the acarid mite, lardoglyphus konoi」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