9a-methyl-1,2,3,4,4a,9a-hexahydro-fluoren-9-one | 13970-34-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 芴
• 英文名称: 9a-methyl-1,2,3,4,4a,9a-hexahydro-fluoren-9-one
• 英文别名: 9a-Methyl-1,2,3,4,4a,9a-hexahydro-fluoren-9-on；9a-methyl-2,3,4,4a-tetrahydro-1H-fluoren-9-one
• CAS: 13970-34-8
• 化学式: C₁₄H₁₆O
• 分子量: 200.28
• InChiKey: FMUSCFPAFAGORZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  15
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  9a-methyl-1,2,3,4,4a,9a-hexahydro-fluoren-9-one 在 N-氯代丁二酰亚胺 、 正丁基锂 作用下， 以 四氢呋喃 、 正己烷 、 二氯甲烷 、 水 为溶剂， 反应 4.5h， 生成 10a-methyl-2,3,4,4a-tetrahydro-1H-phenanthrene-9,10-dione
  参考文献：
  名称：

  A New Redundant Rearrangement of Aromatic Ring Fused Cyclic α-Hydroxydithiane Derivatives. Synthesis of Aromatic Ring Fused Cyclic 1,2-Diketones with One-Carbon Ring Expansion

  摘要：

  A new reaction involving rearrangement of aromatic ring fused cyclic dithiane alcohol by N-chlorosuccinimide in CH2Cl2-H2O to the corresponding one-carbon ring expanded 1,2-diketone has been developed. A wide range of structurally varied dithiane alcohols have been found to undergo this rearrangement in high yields. The general criteria and reaction mechanism for this rearrangement have also been worked out.

  DOI：

  10.1021/jo990634s
• 作为产物：
  描述：

  alkaline earth salt of/the/ methylsulfuric acid 在 氯化亚砜 、 四氯化锡 、 苯 作用下， 生成 9a-methyl-1,2,3,4,4a,9a-hexahydro-fluoren-9-one
  参考文献：
  名称：

  Protiva; Novak, Collection of Czechoslovak Chemical Communications, 1954, vol. 19, p. 541,543

  摘要：

  DOI：

文献信息

• Cyclizations by carbon monoxide in Friedel-Crafts reactions. Facile synthesis of .beta.-disubstituted .alpha.-indanones
  作者：Herman A. Bruson、Howard L. Plant

  DOI：10.1021/jo01286a018

  日期：1967.11
• SCHULTZ, ARTHUR G.;MACIELAG, MARK;PODHOREZ, DAVID E.;SUHADOLNIK, JOSEPH C+, J. ORG. CHEM., 53,(1988) N 11, 2456-2464
  作者：SCHULTZ, ARTHUR G.、MACIELAG, MARK、PODHOREZ, DAVID E.、SUHADOLNIK, JOSEPH C+

  DOI：——

  日期：——
• A New Redundant Rearrangement of Aromatic Ring Fused Cyclic α-Hydroxydithiane Derivatives. Synthesis of Aromatic Ring Fused Cyclic 1,2-Diketones with One-Carbon Ring Expansion
  作者：Brindaban C. Ranu、Umasish Jana

  DOI：10.1021/jo990634s

  日期：1999.8.1

  A new reaction involving rearrangement of aromatic ring fused cyclic dithiane alcohol by N-chlorosuccinimide in CH2Cl2-H2O to the corresponding one-carbon ring expanded 1,2-diketone has been developed. A wide range of structurally varied dithiane alcohols have been found to undergo this rearrangement in high yields. The general criteria and reaction mechanism for this rearrangement have also been worked out.
• Protiva; Novak, Collection of Czechoslovak Chemical Communications, 1954, vol. 19, p. 541,543
  作者：Protiva、Novak

  DOI：——

  日期：——