Synthetic Strategies Towards the Total Synthesis of Phyllanthocin and Breynolide. Application of Stereochemically Linear and Convergent Strategies.

スポンサーリンク

概要

• 論文の詳細を見る

• Phyllanthoside and breynin A are structurally related spiroketal glycoside natural products with potent, interesting and diverse biological activities. Due to their therapeutic potential and novel architecture, the respective aglycones, phyllanthocin and breynolide have attracted significant effort from the synthetic community. This review highlights the synthetic approaches to these targets with an emphasis on the strategy for incorporating the requisite stereogenic centers.

• 社団法人日本薬学会の論文
• 1999-12-15

著者

• Smith Amos

  Department Of Chemistry Monell Chemical Senses Center And Laboratory For Research On The Structure O

• Smith Amos

  Department Of Chemistry The Laboratory For Research On The Structure Of Matter And The Monell Chemic

• EMPFIELD James

  (Current Address)AstraZeneca, A Business Unit of Zeneca Inc.,

• Empfield James

  (current Address)astrazeneca A Business Unit Of Zeneca Inc.

• Smith 3

  Department of Chemistry, The Laboratory for Research on the Structure of Matter and The Monell Chemical Senses Center, University of Pennsylvania

関連論文

• Synthetic Strategies Towards the Total Synthesis of Phyllanthocin and Breynolide. Application of Stereochemically Linear and Convergent Strategies.
• PL-7 EVOLUTION OF THE PETASIS-FERRIER UNION/REARRANGEMENT TACTIC IN TOTAL SYNTHESIS

スポンサーリンク