3-Benzoyl-1-phenylpent-2-ene-1,4-dione | 90043-56-4

• 分子结构分类: 有机化合物 - 木脂素、新木脂素和相关化合物
• 英文名称: 3-Benzoyl-1-phenylpent-2-ene-1,4-dione
• 英文别名: 3-benzoyl-1-phenylpent-2-ene-1,4-dione
• CAS: 90043-56-4
• 化学式: C₁₈H₁₄O₃
• 分子量: 278.307
• InChiKey: KXUJXCFDPLQTPT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  21
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  51.2
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-Benzoyl-1-phenylpent-2-ene-1,4-dione 在 一水合肼 作用下， 以 叔丁醇 为溶剂， 生成 3,6-二苯基哒嗪
  参考文献：
  名称：

  Unexpected C–C Bond Cleavage: A Route to 3,6-Diarylpyridazines and 6-Arylpyridazin-3-ones from 1,3-Dicarbonyl Compounds and Methyl Ketones

  摘要：

  An unexpected C-C bond cleavage has been revealed in the absence of metal. This observation has been exploited to develop an efficient approach toward 3,6-iarylpyridazines and 6-arylpyridazin-3-ones from simple and commercially available 1,3-dicarbonyl compounds and methyl ketones.

  DOI：

  10.1021/jo301751e
• 作为产物：
  描述：

  3,4-二羟基苯乙酮 、 1-苯基-1,3-丁二酮 在 碘 、 copper(II) oxide 作用下， 以 二甲基亚砜 为溶剂， 反应 12.0h， 生成 3-Benzoyl-1-phenylpent-2-ene-1,4-dione
  参考文献：
  名称：

  Unexpected C–C Bond Cleavage: A Route to 3,6-Diarylpyridazines and 6-Arylpyridazin-3-ones from 1,3-Dicarbonyl Compounds and Methyl Ketones

  摘要：

  An unexpected C-C bond cleavage has been revealed in the absence of metal. This observation has been exploited to develop an efficient approach toward 3,6-iarylpyridazines and 6-arylpyridazin-3-ones from simple and commercially available 1,3-dicarbonyl compounds and methyl ketones.

  DOI：

  10.1021/jo301751e

文献信息

• Highly Efficient Synthesis of 3a,6a-Dihydrofuro[2,3-<i>b</i>]furans via a Novel Bicyclization
  作者：Wen-Ming Shu、Yan Yang、Dong-Xue Zhang、Liu-Ming Wu、Yan-Ping Zhu、Guo-Dong Yin、An-Xin Wu

  DOI：10.1021/ol400016c

  日期：2013.2.1

  A highly efficient method for the construction of 3a,6a-dihydrofuro[2,3-b]furan derivatives has been developed via a novel bicyclization, which is very valuable for the synthesis of fused furofuran compounds since it is time-saving and catalyst-free. Based on the bicyclization, a coupled domino strategy has been developed to directly construct 3a,6a-dihydrofuro[2,3-b]furan derivatives from methyl ketones

  通过新型的双环化，已经开发出了一种高效的3a，6a-二氢呋喃[2,3- b ]呋喃衍生物的构建方法，该方法对于合成熔融呋喃呋喃化合物非常节省时间，并且可以催化催化剂。自由。基于双环化，已开发了一种耦合多米诺骨牌策略，可直接从甲基酮构建3a，6a-二氢呋喃[2,3- b ]呋喃衍生物。
• Brønsted acid promoted addition–cyclization and C–C bond cleavage: a convenient synthesis of 2-amino-5-aroylmethylthiazoles derivatives
  作者：Fan Ni、Yan Yang、Wen-Ming Shu、Jun-Rui Ma、An-Xin Wu

  DOI：10.1039/c4ob01519c

  日期：——

  A Brønsted acid promoted C–C bond cleavage method for the synthesis of novel 2-amino-5-aroylmethylthiazole derivatives has been directly developed from 1,4-enediones and thioureas through self-sequenced thio-Michael-addition, intramolecular selective cyclization, dehydration/aromatization, and C–C bond cleavage reactions. It is noteworthy that this reaction has significant advantages in simple reagents, under environmentally benign conditions and with excellent yields. This highly efficient method is also a highly attractive alternative for the preparation of PLTP, CETP inhibitors and novel biheterocycles.

  通过自序的硫代迈克尔加成反应、分子内选择性环化反应、脱水/芳香化反应和 CâC 键裂解反应，从 1,4-enediones 和硫脲类化合物直接开发出了一种布氏酸促进的 CâC 键裂解方法，用于合成新型 2-amino-5-aroylmethylthiazole 衍生物。值得注意的是，该反应具有试剂简单、环境友好、收率高的显著优势。这种高效的方法也是制备 PLTP、CETP 抑制剂和新型生物杂环的极具吸引力的替代方法。
• Unexpected C–C Bond Cleavage: A Route to 3,6-Diarylpyridazines and 6-Arylpyridazin-3-ones from 1,3-Dicarbonyl Compounds and Methyl Ketones
  作者：Qinghe Gao、Yanping Zhu、Mi Lian、Meicai Liu、Jingjing Yuan、Guodong Yin、Anxin Wu

  DOI：10.1021/jo301751e

  日期：2012.11.2

  An unexpected C-C bond cleavage has been revealed in the absence of metal. This observation has been exploited to develop an efficient approach toward 3,6-iarylpyridazines and 6-arylpyridazin-3-ones from simple and commercially available 1,3-dicarbonyl compounds and methyl ketones.