[(1R,4R,5R,8S)-7-(hydroxymethyl)-1-methyl-4-(methylethyl)bicyclo[3.2.1]oct-6-en-8-yl]methan-1-ol | 405157-84-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: [(1R,4R,5R,8S)-7-(hydroxymethyl)-1-methyl-4-(methylethyl)bicyclo[3.2.1]oct-6-en-8-yl]methan-1-ol
• 英文别名: drechslerine A；drechslerin A；[(1R,4R,5R,8S)-7-(hydroxymethyl)-1-methyl-4-propan-2-yl-8-bicyclo[3.2.1]oct-6-enyl]methanol
• CAS: 405157-84-8
• 化学式: C₁₄H₂₄O₂
• 分子量: 224.343
• InChiKey: WCRQEYCIOPEQST-RFGFWPKPSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.86
• 拓扑面积：
  40.5
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  methyl (1S,2R,5R)-8-(methoxymethylene)-5-methyl-2-(methylethyl)-7-[(trifluoromethyl)sulfonyloxy]bicyclo[3.2.1]oct-6-ene-6-carboxylate 在 吗啉 、 甲酸 、 高氯酸 、 三正丁胺 、 palladium diacetate 、 二异丁基氢化铝 、 对甲苯磺酸 、 三苯基膦 作用下， 以 乙醚 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 甲苯 、 乙腈 为溶剂， 反应 26.5h， 生成 [(1R,4R,5R,8S)-7-(hydroxymethyl)-1-methyl-4-(methylethyl)bicyclo[3.2.1]oct-6-en-8-yl]methan-1-ol
  参考文献：
  名称：

  First total syntheses of bicyclic marine sesquiterpenoids drechslerines A and B

  摘要：

  The first total syntheses of the bicyclic sesquiterpenoids drechslerines A (1) and B (2), which were isolated from the algicolous fungus Drechslera dematioidea in the marine red alga Liagora viscida, has been accomplished starting from (S)-carvone (13) via three palladium-catalyzed reactions, namely, diastereoselective allylation, conjugate reduction, and carbon monoxide insertion, as the key reactions. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.04.007

文献信息

• First total syntheses of bicyclic marine sesquiterpenoids drechslerines A and B
  作者：Hisahiro Hagiwara、Masakazu Fukushima、Kimihiko Kinugawa、Takuya Matsui、Takashi Hoshi、Toshio Suzuki

  DOI：10.1016/j.tet.2011.04.007

  日期：2011.6

  The first total syntheses of the bicyclic sesquiterpenoids drechslerines A (1) and B (2), which were isolated from the algicolous fungus Drechslera dematioidea in the marine red alga Liagora viscida, has been accomplished starting from (S)-carvone (13) via three palladium-catalyzed reactions, namely, diastereoselective allylation, conjugate reduction, and carbon monoxide insertion, as the key reactions. (C) 2011 Elsevier Ltd. All rights reserved.