ent-(1¹¹S,5R)-1¹β,1²β-diacetoxy-1⁹β-(2-acetoxy-2-methyl-propionyloxy)-1^5,11-epoxy-1⁴,1⁶α-dihydroxy-1⁸β-(4-hydroxy-3,5-dimethoxy-benzoyloxy)-5r,6t-dimethyl-1¹⁴-(4-methyl-nicotinoyloxy)-(1³βH,1⁷βH)-2,8-dioxa-1(12,3)-eudesmana-4(3,2)-pyridina-cyclooctaphane-3,7-dione | 73257-61-1

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 大环内酯类和类似物
• 英文名称: ent-(1¹¹S,5R)-1¹β,1²β-diacetoxy-1⁹β-(2-acetoxy-2-methyl-propionyloxy)-1^5,11-epoxy-1⁴,1⁶α-dihydroxy-1⁸β-(4-hydroxy-3,5-dimethoxy-benzoyloxy)-5r,6t-dimethyl-1¹⁴-(4-methyl-nicotinoyloxy)-(1³βH,1⁷βH)-2,8-dioxa-1(12,3)-eudesmana-4(3,2)-pyridina-cyclooctaphane-3,7-dione
• 英文别名: O⁹-(2-acetoxy-2-methyl-propionyl)-8α-(4-hydroxy-3,5-dimethoxy-benzoyloxy)-O¹⁵-(4-methyl-nicotinoyl)-O⁶,O⁹,O¹⁵-trideacetyl-8-deoxo-evonine
• CAS: 73257-61-1
• 化学式: C₅₂H₆₀N₂O₂₂
• 分子量: 1065.05
• InChiKey: GWJFZXLNNWQPIT-SLQKACAWSA-N

反应信息

• 作为产物：
  描述：

  Cathedulin E4 在 镍 作用下， 以 乙醇 为溶剂， 生成 ent-(1¹¹S,5R)-1¹β,1²β-diacetoxy-1⁹β-(2-acetoxy-2-methyl-propionyloxy)-1^5,11-epoxy-1⁴,1⁶α-dihydroxy-1⁸β-(4-hydroxy-3,5-dimethoxy-benzoyloxy)-5r,6t-dimethyl-1¹⁴-(4-methyl-nicotinoyloxy)-(1³βH,1⁷βH)-2,8-dioxa-1(12,3)-eudesmana-4(3,2)-pyridina-cyclooctaphane-3,7-dione
  参考文献：
  名称：

  Baxter,R.L. et al., Journal of the Chemical Society. Perkin transactions I, 1979, p. 2982 - 2989

  摘要：

  DOI：