(3aS,4R,6S,7S,7aS,Z)-methyl-7a-methyl-9-oxo-3-(1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethylidene)octahydro-4,7-ethanobenzofuran-6-carboxylate | 1448451-38-4

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (3aS,4R,6S,7S,7aS,Z)-methyl-7a-methyl-9-oxo-3-(1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethylidene)octahydro-4,7-ethanobenzofuran-6-carboxylate
• CAS: 1448451-38-4
• 化学式: C₂₁H₃₁BO₆
• 分子量: 390.285
• InChiKey: VDNUCKHRGREUJZ-FVUAKMEWSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.74
• 重原子数：
  28.0
• 可旋转键数：
  2.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.81
• 拓扑面积：
  71.06
• 氢给体数：
  0.0
• 氢受体数：
  6.0

反应信息

• 作为产物：
  描述：

  (3aS,7aS,Z)-7a-methyl-3-(1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethylidene)-2,3,3a,4-tetrahydrobenzofuran-5(7aH)-one 、 丙烯酸甲酯（MA） 在 lithium hexamethyldisilazane 作用下， 以 四氢呋喃 为溶剂， 反应 0.5h， 以46%的产率得到(3aS,4R,6S,7S,7aS,Z)-methyl-7a-methyl-9-oxo-3-(1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethylidene)octahydro-4,7-ethanobenzofuran-6-carboxylate
  参考文献：
  名称：

  Cu-Catalyzed Asymmetric Borylative Cyclization of Cyclohexadienone-Containing 1,6-Enynes

  摘要：

  The first Cu-catalyzed asymmetric borylative cyclization of cyclohexadienone-containing 1,6-enynes is achieved through a tandem process: selective beta-borylation of propargylic ether and subsequent conjugate addition to cyclohexadienone. The reaction proceeds with excellent regioselectivity and enantioselectivity to afford an optically pure cis-hydrobenzofuran framework bearing alkenylboronate and enone substructures. Furthermore, the resulting bicyclic products could be converted to bridged and tricyclic ring structures. This method extends the realm of Cu-catalyzed asymmetric tandem reactions using bis(pinacolato)diboron (B(2)pin(2)).

  DOI：

  10.1021/ja404593c