(3S,6R)-6-acetoxy-3-(N-1-naphthyl)carbamoyloxy-2,6-dimethylocta-1,7-diene | 252857-35-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: (3S,6R)-6-acetoxy-3-(N-1-naphthyl)carbamoyloxy-2,6-dimethylocta-1,7-diene
• CAS: 252857-35-5
• 化学式: C₂₃H₂₇NO₄
• 分子量: 381.472
• InChiKey: ALKXOPSMTFXVQS-GMAHTHKFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.62
• 重原子数：
  28.0
• 可旋转键数：
  8.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  64.63
• 氢给体数：
  1.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  (3S,6R)-6-acetoxy-3-(N-1-naphthyl)carbamoyloxy-2,6-dimethylocta-1,7-diene 在 甲醇 、 三苯基氢化锡 、 sodium methylate 、 4-甲基苯磺酸吡啶 作用下， 以 二氯甲烷 、 甲苯 为溶剂， 反应 58.0h， 生成 2H-吡喃-3-醇,6-乙烯基四氢-2,2,6-三甲基-,(3S,6R)-
  参考文献：
  名称：

  Enantioselective synthesis of each stereoisomer of the pyranoid linalool oxides: the linalool route

  摘要：

  Each of the four enantiomerically pure tetrahydropyran linalool oxides was prepared by separate enantioselective Sharpless dihydroxylation of (R)- or (S)-linalyl acetate with AD-mix-alpha or AD-mix-beta, followed by a completely stereoselective N-phenylselenophthalimide cyclization of an intermediate allylic alcohol. (C) 1999 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0957-4166(99)00359-6
• 作为产物：
  描述：

  (3S/R,6R)-6-acetoxy-2,6-dimethyloct-7-en-2,3-diol 在 吡啶 、 三氯氧磷 作用下， 以 二氯甲烷 为溶剂， 反应 4.0h， 生成 (3S,6R)-6-acetoxy-3-(N-1-naphthyl)carbamoyloxy-2,6-dimethylocta-1,7-diene
  参考文献：
  名称：

  Enantioselective synthesis of each stereoisomer of the pyranoid linalool oxides: the linalool route

  摘要：

  Each of the four enantiomerically pure tetrahydropyran linalool oxides was prepared by separate enantioselective Sharpless dihydroxylation of (R)- or (S)-linalyl acetate with AD-mix-alpha or AD-mix-beta, followed by a completely stereoselective N-phenylselenophthalimide cyclization of an intermediate allylic alcohol. (C) 1999 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0957-4166(99)00359-6

文献信息

• Enantioselective synthesis of each stereoisomer of the pyranoid linalool oxides: the linalool route
  作者：Giovanni Vidari、Anna Di Rosa、Giuseppe Zanoni、Carlo Bicchi

  DOI：10.1016/s0957-4166(99)00359-6

  日期：1999.9

  Each of the four enantiomerically pure tetrahydropyran linalool oxides was prepared by separate enantioselective Sharpless dihydroxylation of (R)- or (S)-linalyl acetate with AD-mix-alpha or AD-mix-beta, followed by a completely stereoselective N-phenylselenophthalimide cyclization of an intermediate allylic alcohol. (C) 1999 Elsevier Science Ltd. All rights reserved.