Synthetic studies on thiostrepton family of peptide antibiotics: Synthesis of the cyclic core portion containing the dehydropiperidine, dihydroquinoline, L-valine, and masked dehydroalanine segments

Tomonori Mori, Hiraku Tohmiya, Yukiko Satouchi, Shuhei Higashibayashi, Kimiko Hashimoto, Masaya Nakata

研究成果: Article査読

16 被引用数 (Scopus)

抄録

The cyclic core portion containing the dehydropiperidine, dihydroquinoline, L-valine, and masked dehydroalanine (i.e., β-phenylselenoalanine) segments of the thiostrepton family of peptide antibiotics was synthesized via the consecutive coupling of these four segments followed by cyclization at the amide bond between the dehydropiperidine and masked dehydroalanine segments.

本文言語English
ページ(範囲)6423-6427
ページ数5
ジャーナルTetrahedron Letters
46
38
DOI
出版ステータスPublished - 2005 9月 19

ASJC Scopus subject areas

  • 生化学
  • 創薬
  • 有機化学

フィンガープリント

「Synthetic studies on thiostrepton family of peptide antibiotics: Synthesis of the cyclic core portion containing the dehydropiperidine, dihydroquinoline, L-valine, and masked dehydroalanine segments」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