Synthetic Studies of Polycyclic Terpenoids Using the Intramolecular Aldol-Type Cyclization Reaction

DOI Web Site Web Site 被引用文献1件 参考文献59件
  • 小林 豊晴
    School of Life Sciences, Tokyo University of Pharmacy and Life Sciences
  • 阿部 秀樹
    Department of Chemical and Biological Sciences, Faculty of Science, Japan Women’s University
  • 伊藤 久央
    School of Life Sciences, Tokyo University of Pharmacy and Life Sciences

この論文をさがす

抄録

<p>Our four recent synthetic studies of polycyclic terpenoids using the intramolecular aldol type cyclization reaction are described. (i) Asymmetric total synthesis of tricyclic diterpenoid spirocurcasone using an intramolecular aldol condensation to construct the bicyclic ring system. (ii) Total synthesis of tricyclic sesquiterpenoid albaflavenone using sequential intramolecular aldol condensations to construct its tricyclic framework. (iii) Total synthesis of paralemnolide A using an intramolecular Reformatsky-Honda reaction to construct the tricyclic framework. (iv) Synthetic study of marine diterpenoid aberrarone using a repeated 1,4-addition followed by intramolecular aldol reaction protocol to construct the tetracyclic framework.</p>

収録刊行物

被引用文献 (1)*注記

もっと見る

参考文献 (59)*注記

もっと見る

キーワード

詳細情報 詳細情報について

問題の指摘

ページトップへ