(S,E)-7-methoxytetradec-4-en-1-ol | 142088-55-9

• 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: (S,E)-7-methoxytetradec-4-en-1-ol
• 英文别名: (E,7S)-7-methoxytetradec-4-en-1-ol
• CAS: 142088-55-9
• 化学式: C₁₅H₃₀O₂
• 分子量: 242.402
• InChiKey: KFRIZIICEJZEAP-VSGCLNPGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  17
• 可旋转键数：
  12
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.87
• 拓扑面积：
  29.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (S,E)-7-methoxytetradec-4-en-1-ol 在 Jones reagent 、 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 以 二氯甲烷 、 丙酮 为溶剂， 反应 12.0h， 生成 (E,7S)-7-methoxy-N-(2-methylpropyl)tetradec-4-enamide
  参考文献：
  名称：

  Novel malyngamide structural analogs: synthesis and biological evaluation

  摘要：

  In the course of our search for new anticancer agents, a series of novel malyngamide derivatives were synthesized by sharpless asymmetric epoxidation, followed by Julia-Kocinski olefination reactions as key reaction sequence. Anticancer activities of all these derivatives were screened against IMR-32, SF-295, SKNSH, HeLa, Colon-502713, SW-620, and Hop-62 cell lines for the first time.

  DOI：

  10.1007/s00044-013-0466-y
• 作为产物：
  描述：

  (S,E)-2-(7-methoxytetradec-4-enyloxy)-tetrahydro-2H-pyran 在 4-甲基苯磺酸吡啶 乙醇 作用下， 生成 (S,E)-7-methoxytetradec-4-en-1-ol
  参考文献：
  名称：

  （4E）-7-甲氧基十四烷基-4-烯酸的合成：一种来自天竺葵的新型脂肪酸

  摘要：

  描述了（4E）-7-甲氧基十四烷基-4-烯酸的合成。在蓝绿色藻类中发现了这种新的脂肪酸。并作为酰胺掺入几种含氮代谢产物中，包括鱼类拒食化合物麦芽酰胺A。

  DOI：

  10.1016/s0040-4039(00)74202-x

文献信息

• Synthesis of (4E)-7-methoxytetradec-4-enoic acid: a novel fatty acid from lyngbya majuscula
  作者：Craig B. Fryhle、Paul G. Williard、Rybak Carol M.

  DOI：10.1016/s0040-4039(00)74202-x

  日期：1992.4

  The synthesis of (4E)-7-methoxytetradec-4-enoic acid is described. This novel fatty acid is found in the blue-green algae . and is incorporated as the amide in several nitrogeneous metabolites, including the fish antifeedant compound malyngamide A.

  描述了（4E）-7-甲氧基十四烷基-4-烯酸的合成。在蓝绿色藻类中发现了这种新的脂肪酸。并作为酰胺掺入几种含氮代谢产物中，包括鱼类拒食化合物麦芽酰胺A。
• Total synthesis of malyngamide M and isomalyngamide M
  作者：Jie Chen、Zi-Fa Shi、Ling Zhou、An-Le Xie、Xiao-Ping Cao

  DOI：10.1016/j.tet.2010.03.004

  日期：2010.5

  The stereoselective synthesis of malyngamide M (1) was accomplished in nine steps from o-cresol in 12% overall yield. The key steps involved the Wittig reaction of an α-NHBoc aryl ketone 4 for the introduction of vinyl chloride functionality, an amidation of lyngbic acid 3 with a secondary amine 2 for the framework of target molecule, and an isomerization of a (Z)-vinyl chloride to the (E)-configuration

  麦芽酰胺M（1）的立体选择性合成是从邻甲酚开始的9个步骤，总产率为12％。关键步骤包括用于引入氯乙烯官能团的α- NHBoc芳基酮4的Wittig反应，针对目标分子框架的lyngbic acid 3与仲胺2的酰胺化以及（Z）-的异构化使用二苯甲酮作为光敏剂将氯乙烯制成（E）-构型。还合成了异麦芽酰胺M（Z - 1）。
• Convenient synthesis of (±)- and (S)-antipode of (4E,7S)-7-methoxytetradec-4-enoic acid, the antimicrobial principle of marine cyanophyte
  作者：S. Sankaranarayanan、Anubha Sharma、Subrata Chattopadhyay

  DOI：10.1016/0957-4166(96)00339-4

  日期：1996.9

  The (+/-)- and S-isomers of title compound I were prepared via a short and efficient route. The key features of the synthesis were the use of easily accessible materials, operationally simple reaction protocol and highly enantioselective lipase catalyzed esterification for the generation of the required chiron. Copyright (C) 1996 Published by Elsevier Science Ltd
• Total synthesis of malyngamide X and its 7′S-epi isomer
  作者：Suchada Suntornchashwej、Khanit Suwanborirux、Minoru Isobe

  DOI：10.1016/j.tet.2007.01.035

  日期：2007.4

  Stereoselective syntheses of malyngamide X (1) and its 7'(S)-epimer are described. A Lewis acid (Et2AlCl) mediated anti-aldol reaction was employed to generate the stereocenters C-7 and C-8. The route is convergent and provides a convenient access to the synthesis of structural variants of malyngamide X. Stereochemistry at C-7' in the molecules of natural and synthetic 1, and 7'(S)-epi 1 was confirmed by NMR chiral solvation experiments. (c) 2007 Elsevier Ltd. All rights reserved.
• A concise total synthesis of lyngbic acid, hermitamides A and B
  作者：S. Satyanarayana、B.V. Subba Reddy、R. Narender

  DOI：10.1016/j.tetlet.2014.08.125

  日期：2014.10

  A concise total syntheses of lyngbic acid, hermitamides A and B have been accomplished in a highly enantioselective manner involving CBS asymmetric reduction, hydroboration, and stereospecific Julia-Lythgoe olefination. (C) 2014 Published by Elsevier Ltd.