Synthetic studies on biologically active alkaloids starting from lactam-type chiral building blocks

Naoki Toyooka*, Hideo Nemoto

*この論文の責任著者

研究成果: 書籍の章/レポート/会議録査読

25 被引用数 (Scopus)

抄録

This review describes synthetic studies on biologically active alkaloids starting from three lactams. A stereodivergent process for the synthesis of 3-piperidinol alkaloids and the total synthesis of cytotoxic marine alkaloids, clavepictines A, B, pictamine, and lepadin B, were achieved starting from our original lactam-type chiral building block1. The synthesis of the proposed structure for dart-poison frog alkaloid223A and a stereodivergent process for the synthesis of decahydroquinoline-type dart-poison frog alkaloids were achieved from lactam31. Finally, synthesis of the revised structure for the above alkaloid223A and dart-poison frog alkaloid2071 was also achieved starting from lactam68.

本文言語英語
ホスト出版物のタイトルStudies in Natural Products Chemistry
出版社Elsevier
ページ419-448
ページ数30
PART J
DOI
出版ステータス出版済み - 2003

出版物シリーズ

名前Studies in Natural Products Chemistry
番号PART J
29
ISSN(印刷版)1572-5995

ASJC Scopus 主題領域

  • 創薬
  • 有機化学

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