(2aα,5β,6aβ,7aβ,7bα,7cα)-(+/-)-6-ethenyl-2a,3,4,5,6a,7a,7b,7c-octahydro-5-<<(methylsulfonyl)oxy>methyl>-2a-methyl-2H-oxireno<2,3>naphtho<1,8-bc>furan-2-one | 143495-24-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 内酯类
• 英文名称: (2aα,5β,6aβ,7aβ,7bα,7cα)-(+/-)-6-ethenyl-2a,3,4,5,6a,7a,7b,7c-octahydro-5-<<(methylsulfonyl)oxy>methyl>-2a-methyl-2H-oxireno<2,3>naphtho<1,8-bc>furan-2-one
• 英文别名: [(1S,4S,7R,10S,12R,13R)-9-ethenyl-4-methyl-3-oxo-2,11-dioxatetracyclo[6.4.1.04,13.010,12]tridec-8-en-7-yl]methyl methanesulfonate
• CAS: 143495-24-3
• 化学式: C₁₆H₂₀O₆S
• 分子量: 340.397
• InChiKey: YWKSIGOTOCVJDL-HPWNFOQCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.69
• 拓扑面积：
  90.6
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  (2aα,5β,6aβ,7aβ,7bα,7cα)-(+/-)-6-ethenyl-2a,3,4,5,6a,7a,7b,7c-octahydro-5-<<(methylsulfonyl)oxy>methyl>-2a-methyl-2H-oxireno<2,3>naphtho<1,8-bc>furan-2-one 在 (trimethylstannyl)lithium 、 4-二甲氨基吡啶 、 sodium hydroxide 、 重铬酸吡啶 、 偶氮二异丁腈 、 碘苯二乙酸 、 Celite 、 双氧水 、 碘 、 三正丁基氢锡 、 二异丁基氢化铝 、 戴斯-马丁氧化剂 、 N,N'-二环己基碳二亚胺 作用下， 以 四氢呋喃 、 甲醇 、 乙醚 、 二氯甲烷 、 环己烷 、 甲苯 、 苯 为溶剂， 反应 20.75h， 生成 (2aα,4aα,5aR*,7α,9aR*,9bR*,9cα,10aα)-(+/-)-7-ethenyldecahydro-2a,7-dimethyl-5a,9a-epoxy-3H-cyclopropa<4,4a>phenanthro<10,1-bc>furan-3,5(1H)-dione
  参考文献：
  名称：

  Total Synthesis of (.+-.)-Myrocin C

  摘要：

  A stereoselective total synthesis of racemic myrocin C (1) has been achieved. Initial investigations produced cyclopropane-containing AB sector 22 via intramolecular ester-tethered Diels-Alder reaction of quinone 14 followed by internal alkylation of bromide 19. Although the natural product was not to be obtained through this route, the information garnered from this impetus provided the basis for a strategically improved and ultimately successful synthesis of 1. Thus, intermolecular Diels-Alder reaction of p-benzoquinone with cyclic diene 39 gave endo cycloadduct 41 which could be elaborated to cyclopropane precursors 52 and 99. While a plethora of intramolecular alkylation reactions of derivatives of 52 failed to afford cyclopropane-containing products, a novel organolithium-induced cyclization reaction of 99 did indeed provide key compound 96 via postulated intermediate 100. The resultant functionality in 96 paved the way for a directed intramolecular Diels-Alder annulation of the C-ring and concomitant introduction of the remote quaternary C13 stereocenter (cf. 96 --> 107 --> 108). The tertiary hydroxyl group at C9 was then introduced via epoxidation of 119 followed by overall eliminative ring-opening (123 --> 125 --> 5). The incorporation of the C6 tertiary hydroxyl group was accomplished via oxidation of the enolate derived from 6-desoxymyrocin C (5), yielding racemic 1. Studies on the bioactivation process of 5 and 1 led to support for a hypothesis which emphasized the importance of the C6 hydroxyl group in facilitating cyclopropane-ring-opening possibly through the intermediacy of quinone homomethide 134.

  DOI：

  10.1021/ja00104a002
• 作为产物：
  描述：

  (2aα,5β,6aβ,7aβ,7bα,7cα)-(+/-)-5-<<(tert-butyldimethylsilyl)oxy>methyl>-2a,3,4,5,6a,7a,7b,7c-octahydro-2a-methyl-2-oxo-2H-oxireno<2,3>naphtho<1,8-bc>furan-6-yl trifluoromethanesulfonate 在 4-二甲氨基吡啶 、 bis-triphenylphosphine-palladium(II) chloride 、 四丁基氟化铵 、 三乙胺 、 lithium chloride 作用下， 以 四氢呋喃 、 二氯甲烷 、 溶剂黄146 为溶剂， 生成 (2aα,5β,6aβ,7aβ,7bα,7cα)-(+/-)-6-ethenyl-2a,3,4,5,6a,7a,7b,7c-octahydro-5-<<(methylsulfonyl)oxy>methyl>-2a-methyl-2H-oxireno<2,3>naphtho<1,8-bc>furan-2-one
  参考文献：
  名称：

  A remarkable cyclopropanation: the total synthesis of myrocin C

  摘要：

  DOI：

  10.1021/ja00047a079

文献信息

• A remarkable cyclopropanation: the total synthesis of myrocin C
  作者：Margaret Y. Chu-Moyer、Samuel J. Danishefsky

  DOI：10.1021/ja00047a079

  日期：1992.10
• Total Synthesis of (.+-.)-Myrocin C
  作者：Margaret Y. Chu-Moyer、Samuel J. Danishefsky、Gayle K. Schulte

  DOI：10.1021/ja00104a002

  日期：1994.12

  A stereoselective total synthesis of racemic myrocin C (1) has been achieved. Initial investigations produced cyclopropane-containing AB sector 22 via intramolecular ester-tethered Diels-Alder reaction of quinone 14 followed by internal alkylation of bromide 19. Although the natural product was not to be obtained through this route, the information garnered from this impetus provided the basis for a strategically improved and ultimately successful synthesis of 1. Thus, intermolecular Diels-Alder reaction of p-benzoquinone with cyclic diene 39 gave endo cycloadduct 41 which could be elaborated to cyclopropane precursors 52 and 99. While a plethora of intramolecular alkylation reactions of derivatives of 52 failed to afford cyclopropane-containing products, a novel organolithium-induced cyclization reaction of 99 did indeed provide key compound 96 via postulated intermediate 100. The resultant functionality in 96 paved the way for a directed intramolecular Diels-Alder annulation of the C-ring and concomitant introduction of the remote quaternary C13 stereocenter (cf. 96 --> 107 --> 108). The tertiary hydroxyl group at C9 was then introduced via epoxidation of 119 followed by overall eliminative ring-opening (123 --> 125 --> 5). The incorporation of the C6 tertiary hydroxyl group was accomplished via oxidation of the enolate derived from 6-desoxymyrocin C (5), yielding racemic 1. Studies on the bioactivation process of 5 and 1 led to support for a hypothesis which emphasized the importance of the C6 hydroxyl group in facilitating cyclopropane-ring-opening possibly through the intermediacy of quinone homomethide 134.