8-Fluoro-4,9,12,15,15-pentamethyl-19-(trimethylsilyl)-4(E),8(Z),12(Z)-nonadecatrien-17-ynal | 155016-92-5

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 8-Fluoro-4,9,12,15,15-pentamethyl-19-(trimethylsilyl)-4(E),8(Z),12(Z)-nonadecatrien-17-ynal
• 英文别名: (4E,8Z,12Z)-8-fluoro-4,9,12,15,15-pentamethyl-19-trimethylsilylnonadeca-4,8,12-trien-17-ynal
• CAS: 155016-92-5
• 化学式: C₂₇H₄₅FOSi
• 分子量: 432.738
• InChiKey: YHMRASYMJHPZHQ-UJZQJGEWSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.81
• 重原子数：
  30
• 可旋转键数：
  13
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  8-Fluoro-4,9,12,15,15-pentamethyl-19-(trimethylsilyl)-4(E),8(Z),12(Z)-nonadecatrien-17-ynal 在 六甲基磷酰三胺 、 magnesium bromide 、 lithium diisopropyl amide 作用下， 以 四氢呋喃 、 乙醚 为溶剂， 反应 76.1h， 生成
  参考文献：
  名称：

  作为环氧化物的替代物的四甲基烯丙基阳离子起仿生多烯五环化的引发剂的作用。槐糖二醇的全合成

  摘要：

  四甲基烯丙基阳离子已被证明是环氧化物的有效替代品，可作为仿生多烯环化反应的引发剂。该方法学应用于五环三萜类槐糖二醇（1）的全合成，其中该策略的关键步骤涉及质子酸催化的四甲基烯丙醇9的五环化反应，该产物以31％的收率提供了氟五环11作为主要产物。路易斯酸催化的9的环化反应以50％的收率得到了脱氟化氢的五环化合物12。

  DOI：

  10.1016/s0040-4039(00)76734-7
• 作为产物：
  描述：

  8-Fluoro-4,9,12,15,15-pentamethyl-19-(trimethylsilyl)-4(E),8(Z),12(Z)-nonadecatrien-17-ynenitrile 在 二异丁基氢化铝 作用下， 以93%的产率得到8-Fluoro-4,9,12,15,15-pentamethyl-19-(trimethylsilyl)-4(E),8(Z),12(Z)-nonadecatrien-17-ynal
  参考文献：
  名称：

  Epoxide-initiated cationic polyene cyclisations

  摘要：

  The Lewis acid (2-propoxy)titanium trichloride is an efficient reagent for epoxide-initiated polyene cyclisations. Thus, 4 underwent tricyclisation to yield tricyclic products 5-7 in 73 % yield. The tetraene epoxide 1 gave pentacycle 15 in 21 % yield. The latter is the first example of a cationic pentacarbocyclisalion.

  DOI：

  10.1016/s0040-4039(00)61492-2

文献信息

• Epoxide-initiated cationic polyene cyclisations
  作者：Paul V. Fish、Anantha R. Sudhakar、William S. Johnson

  DOI：10.1016/s0040-4039(00)61492-2

  日期：1993.12

  The Lewis acid (2-propoxy)titanium trichloride is an efficient reagent for epoxide-initiated polyene cyclisations. Thus, 4 underwent tricyclisation to yield tricyclic products 5-7 in 73 % yield. The tetraene epoxide 1 gave pentacycle 15 in 21 % yield. The latter is the first example of a cationic pentacarbocyclisalion.
• The First Examples of Nonenzymic, Biomimetic Polyene Pentacyclizations. Total Synthesis of the Pentacyclic Triterpenoid Sophoradiol
  作者：Paul V. Fish、William S. Johnson

  DOI：10.1021/jo00088a011

  日期：1994.5

  The first examples of nonenzymic, biomimetic, polyene pentacyclizations are reported. A series of closely related (E,E,Z,Z)-polyenes 10-13 with the same tetraene carbon backbone but with differing initiator groups were synthesized and cyclized. The polyenes 10-12 were all synthesized from the known bromo triene 14 using established protocol, Polyene 13 was prepared from aldehyde 16 by reaction of 16 with (l-methyl-l-cyclopropyl)magnesium bromide to give cyclopropylcarbinol 21. Rearrangement of 21 with MgBr2 to bromide 22 and then alkylation of the lithium enolate of ethyl 3,3-dimethylacrylate with 22 furnished 23. Isomerization of the double bond into conjugation with the ester and dimethylation of enoate 24 gave 13. Polyene acetal 10 was cyclized with SnCl4 to pentacycles 26 (4 beta:4 alpha, 5.5:1) in 51% isolated yield accompanied by regiospecific in situ dehydrofluorination. Polyene 11, with the aldehyde initiator, was cyclized with SnCl4 to yield alcohols 27 (4 beta:4 alpha, 5.4:1) in 49% yield, again with loss of HF. Cyclization of the epoxide 12 using the preferred conditions of (i-PrO)TiCl3 as the Lewis acid gave pentacycle 28 as a major product (GC yield, 21%; 10% isolated) along with the bicyclic ether 29 (13%) and backbone-rearranged bicyclic triene 30 (24%). The protic acid-catalyzed cyclization of tetramethylallyl alcohol 13 furnished fluoropentacycle 33 as the major product in 31% yield. In contrast, the Lewis acid-catalyzed cyclization of 13 gave the dehydrofluorinated pentacycle 32 in 50% yield. Fluoropentacycle 33 was converted to sophoradiol (3), a biologically active pentacyclic triterpenoid of the oleanane series, by oxidative cleavage of the C3 isopropylidene and C22 vinylidene groups, regiospecific dehydrofluorination to introduce the C12-13 alkene, and finally stereoselective reduction of diketone 35. The conversion of 13 --> 33 --> 3 has demonstrated that the tetramethylallylic alchol group is an effective substitute for the epoxide (cf. 12 --> 28) as an initiator of biomimetic polyene cyclizations.
• The tetramethylallyl cation as a surrogate for the epoxide function as an initiator of biomimetic polyene pentacyclizations. Total synthesis of sophoradiol
  作者：Paul V Fish、William S Johnson

  DOI：10.1016/s0040-4039(00)76734-7

  日期：1994.3

  The tetramethylallyl cation has proven to be an effective substitute for the epoxide as an initiator for biomimetic polyene cyclizations. This methodology was applied to the total synthesis of the pentacyclic triterpenoid sophoradiol (1) whereby the key step of the strategy involved the protic acid-catalyzed pentacyclization of tetramethylallyl alcohol 9 which furnished fluoropentacycle 11 as the major

  四甲基烯丙基阳离子已被证明是环氧化物的有效替代品，可作为仿生多烯环化反应的引发剂。该方法学应用于五环三萜类槐糖二醇（1）的全合成，其中该策略的关键步骤涉及质子酸催化的四甲基烯丙醇9的五环化反应，该产物以31％的收率提供了氟五环11作为主要产物。路易斯酸催化的9的环化反应以50％的收率得到了脱氟化氢的五环化合物12。