(E,2S,3R,4S)-2-[(4S,5S)-5-[(4-methoxyphenyl)methoxymethyl]-2,2-dimethyl-1,3-dioxan-4-yl]-4,6-dimethyl-8-phenylmethoxyoct-6-en-3-ol | 753016-65-8

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: (E,2S,3R,4S)-2-[(4S,5S)-5-[(4-methoxyphenyl)methoxymethyl]-2,2-dimethyl-1,3-dioxan-4-yl]-4,6-dimethyl-8-phenylmethoxyoct-6-en-3-ol
• CAS: 753016-65-8
• 化学式: C₃₂H₄₆O₆
• 分子量: 526.714
• InChiKey: GUVLAVOCYITKGP-SDYJUGQNSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.8
• 重原子数：
  38
• 可旋转键数：
  14
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  66.4
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  (E,2S,3R,4S)-2-[(4S,5S)-5-[(4-methoxyphenyl)methoxymethyl]-2,2-dimethyl-1,3-dioxan-4-yl]-4,6-dimethyl-8-phenylmethoxyoct-6-en-3-ol 在 2,6-二甲基吡啶 、 2,3-二氯-5,6-二氰基-1,4-苯醌 作用下， 生成 (4R,5S)-4-[(E,2R,3R,4S)-3-[tert-butyl(dimethyl)silyl]oxy-4,6-dimethyl-8-phenylmethoxyoct-6-en-2-yl]-2,2-dimethyl-1,3-dioxane-5-carbaldehyde
  参考文献：
  名称：

  A practical synthesis of (−)-kazusamycin A (revised)

  摘要：

  We describe herein a stereo-controlled and practical synthesis of three key building blocks, namely Segment AB', Segment D, and Segment E' needed for the total synthesis of (-)-kazusamycin A. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2005.07.029
• 作为产物：
  描述：

  2-hydroxymethyl-1-(4-methoxybenzyloxy)-3-pentanone 在 咪唑 、 sodium tetrahydroborate 、 tin(II) trifluoromethanesulfonate 、 乙酸乙烯酯 、 lipase AK 、 二乙基甲氧基硼烷 、 四丁基氟化铵 、 4-甲基苯磺酸吡啶 、 三乙胺 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 生成 (E,2S,3R,4S)-2-[(4S,5S)-5-[(4-methoxyphenyl)methoxymethyl]-2,2-dimethyl-1,3-dioxan-4-yl]-4,6-dimethyl-8-phenylmethoxyoct-6-en-3-ol
  参考文献：
  名称：

  A practical synthesis of (−)-kazusamycin A (revised)

  摘要：

  We describe herein a stereo-controlled and practical synthesis of three key building blocks, namely Segment AB', Segment D, and Segment E' needed for the total synthesis of (-)-kazusamycin A. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2005.07.029

文献信息

• First Total Synthesis of the Antitumor Compound (−)-Kazusamycin A and Absolute Structure Determination
  作者：Noriyoshi Arai、Noriko Chikaraishi、Satoshi Omura、Isao Kuwajima

  DOI：10.1021/ol049219z

  日期：2004.8.1

  The first total synthesis of kazusamycin A, a potent antitumor compound from an actinomycete, has been achieved, and its absolute structure was determined. Paterson's stereoselective aldol reaction was successfully applied to construct the contiguous chiral centers by using an originally designed optically active 2-acyl-1,3-propanediol derivative.
• A practical synthesis of (−)-kazusamycin A (revised)
  作者：Shengfeng Zhou、Huaxiang Chen、Wensheng Liao、Shu-Hui Chen、Ge Li、Ryoichi Ando、Isao Kuwajima

  DOI：10.1016/j.tetlet.2005.07.029

  日期：2005.9

  We describe herein a stereo-controlled and practical synthesis of three key building blocks, namely Segment AB', Segment D, and Segment E' needed for the total synthesis of (-)-kazusamycin A. (c) 2005 Elsevier Ltd. All rights reserved.