(2R,3R,4S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-4-(((4-methoxybenzyl)oxy)methyl)-2-methylhex-5-en-3-ol | 1352952-96-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 三苯基化合物
• 英文名称: (2R,3R,4S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-4-(((4-methoxybenzyl)oxy)methyl)-2-methylhex-5-en-3-ol
• CAS: 1352952-96-5
• 化学式: C₃₇H₄₂O₆
• 分子量: 582.737
• InChiKey: VSXMSVSOBHJXPZ-ISXZTQCNSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.04
• 重原子数：
  43.0
• 可旋转键数：
  16.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  66.38
• 氢给体数：
  1.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  (2R,3R,4S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-4-(((4-methoxybenzyl)oxy)methyl)-2-methylhex-5-en-3-ol 在 sodium periodate 、 四氧化锇 、 水 、 N-甲基吗啉氧化物 、 N,N-二异丙基乙胺 作用下， 以 二氯甲烷 、 水 、 丙酮 为溶剂， 反应 1.0h， 生成 (2S,3R,4R)-5-[bis(4-methoxyphenyl)-phenylmethoxy]-2-[(4-methoxyphenyl)methoxymethyl]-4-methyl-3-triethylsilyloxypentanal
  参考文献：
  名称：

  Stereoselective synthesis of a fully protected C13–C23 fragment of tedanolide

  摘要：

  The combination of a high-yielding dienyllithium addition and a highly diastereoselective 1,2-reduction allows the preparation of the completely protected C-13-C-23 fragment 3 of the potent cytotoxic agent tedanolide 1. A convergent approach was used, namely a late stage coupling of the dienyllithium 16 with the selectively protected aldehyde 5 followed by oxidation-reduction and final epoxidation to give 3. The dienylstannane 4 was prepared from the dibromide 6 in five steps, the key step being the highly regio-and stereoselective stannylcupration of the alkyne 7. The commercially available hydroxy ester 10 was converted in 11 steps to the aldehyde 5. The compound 3 could potentially be a key intermediate for the synthesis of tedanolide 1. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.10.024
• 作为产物：
  描述：

  [(2R,3R)-3-[(2R)-1-[bis(4-methoxyphenyl)-phenylmethoxy]propan-2-yl]oxiran-2-yl]methanol 在 copper(I) bromide dimethylsulfide complex 、 sodium hydride 作用下， 以 四氢呋喃 、 乙醚 、 mineral oil 为溶剂， 反应 24.5h， 生成 (2R,3R,4S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-4-(((4-methoxybenzyl)oxy)methyl)-2-methylhex-5-en-3-ol
  参考文献：
  名称：

  Stereoselective synthesis of a fully protected C13–C23 fragment of tedanolide

  摘要：

  The combination of a high-yielding dienyllithium addition and a highly diastereoselective 1,2-reduction allows the preparation of the completely protected C-13-C-23 fragment 3 of the potent cytotoxic agent tedanolide 1. A convergent approach was used, namely a late stage coupling of the dienyllithium 16 with the selectively protected aldehyde 5 followed by oxidation-reduction and final epoxidation to give 3. The dienylstannane 4 was prepared from the dibromide 6 in five steps, the key step being the highly regio-and stereoselective stannylcupration of the alkyne 7. The commercially available hydroxy ester 10 was converted in 11 steps to the aldehyde 5. The compound 3 could potentially be a key intermediate for the synthesis of tedanolide 1. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.10.024