7-methyl-2-phenylchroman-4-one | 64919-60-4

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 黄酮类化合物
• 英文名称: 7-methyl-2-phenylchroman-4-one
• 英文别名: 7-methyl-2-phenyl-2,3-dihydrochromen-4-one
• CAS: 64919-60-4
• 化学式: C₁₆H₁₄O₂
• 分子量: 238.286
• InChiKey: FNOKOVWLKVWYRY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  18
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  7-methyl-2-phenylchroman-4-one 在 sodium tetrahydroborate 作用下， 以 甲醇 为溶剂， 反应 2.0h， 生成 (2R,3S,4S)-3-Chloro-7-methyl-2-phenyl-chroman-4-ol
  参考文献：
  名称：

  Weber; Birkner; Koppel, Pharmazie, 1980, vol. 35, # 5-6, p. 328 - 329

  摘要：

  DOI：
• 作为产物：
  描述：

  2-hydroxy-4'-methyl-chalcone 在 sodium hydroxide 作用下， 生成 7-methyl-2-phenylchroman-4-one
  参考文献：
  名称：

  Cramer; Elschnig, Chemische Berichte, 1956, vol. 89, p. 1,10

  摘要：

  DOI：

文献信息

• Divergent synthesis of flavones and flavanones from 2′-hydroxydihydrochalcones <i>via</i> palladium(<scp>ii</scp>)-catalyzed oxidative cyclization
  作者：Seung Hwan Son、Yang Yil Cho、Hyung-Seok Yoo、Soo Jin Lee、Young Min Kim、Hyu Jeong Jang、Dong Hwan Kim、Jeong-Won Shin、Nam-Jung Kim

  DOI：10.1039/d1ra01672e

  日期：——

  Divergent and versatile synthetic routes to flavones and flavanones via efficient Pd(II) catalysis are disclosed. These Pd(II) catalyses expediently provide a variety of flavones and flavanones from 2′-hydroxydihydrochalcones as common intermediates, depending on oxidants and additives, via discriminate oxidative cyclization sequences involving dehydrogenation, respectively, in a highly atom-economic

  公开了通过有效的 Pd( II ) 催化合成黄酮和黄烷酮的不同且通用的合成路线。根据氧化剂和添加剂，这些 Pd( II ) 催化剂分别以高度原子经济的方式通过涉及脱氢的区分氧化环化序列，方便地从 2'-羟基二氢查耳酮中提供各种黄酮和黄烷酮作为常见的中间体。
• Convenient synthesis of flavanone derivatives via oxa-Michael addition using catalytic amount of aqueous cesium fluoride
  作者：Motofumi Miura、Karin Shigematsu、Masaharu Toriyama、Shigeyasu Motohashi

  DOI：10.1016/j.tetlet.2021.153480

  日期：2021.11

  flavanones, which included polycyclic aromatic and heterocyclic rings, were readily synthesized via oxa-Michael addition from the corresponding hydroxychalcones with a catalytic amount of aqueous cesium fluoride solution under mild conditions. This method could be applied to the scalable synthesis of eriodictyol as a known potent inhibitor of the SARS-CoV-2 spike protein.

  在温和条件下，从相应的羟基查耳酮与催化量的氟化铯水溶液通过氧杂-迈克尔加成容易合成总共 36 种黄烷酮，其中包括多环芳环和杂环。该方法可用于作为 SARS-CoV-2 刺突蛋白的已知强效抑制剂圣草酚的可扩展合成。
• Catalytic enantioselective synthesis of flavanones and chromanones
  申请人：Scheidt Karl

  公开号：US20090259055A1

  公开（公告）日：2009-10-15

  Various chromanone, flavanone and abyssinone compounds as can be prepared enantioselectively using a chiral thiourea catalyst.

  可以使用手性硫脲催化剂对各种色酮、黄酮和阿比西农化合物进行对映选择性合成。
• Palladium-Catalyzed [3+3] Annulation of Vinyl Chromium(0) Carbene Complexes through Carbene Migratory Insertion/Tsuji-Trost Reaction
  作者：Kang Wang、Yifan Ping、Taiwei Chang、Jianbo Wang

  DOI：10.1002/anie.201707590

  日期：2017.10.9

  Vinyl chromium(0) Fischer carbene complexes were employed as the source of π‐allylic palladium species for catalytic [3+3] annulation under palladium catalysis. Mechanistically, this transformation is proposed to involve carbene migratory insertion and intramolecular Tsuji–Trost reaction as the key steps. Substituted six‐membered heterocyclic flavonones and quinolines are obtained, depending on the

  乙烯基铬（0）菲舍尔卡宾络合物被用作π烯丙基钯物质的来源，用于钯催化下的催化[3 + 3]环化。从机理上讲，这种转化被认为包括卡宾迁移插入和分子内Tsuji-Trost反应作为关键步骤。根据偶联伙伴上的亲核官能团，获得了取代的六元杂环黄酮和喹啉。
• Highly Selective Palladium-Catalyzed Direct CH α-Monoarylation of Carbonyl Compounds using Water Containing the Surfactant Polyoxyethylene-α-Tocopheryl Sebacate (PTS) as a Solvent
  作者：Marco Lessi、Tiziana Masini、Luca Nucara、Fabio Bellina、Renzo Rossi

  DOI：10.1002/adsc.201000810

  日期：2011.2.11

  Highly selective direct CH α-monoarylation reactions of 4-chromanones, ketones and 2-phenylacetaldehyde with aryl halides have been performed in satisfactory yields by using a tris(dibenzylideneacetone)dipalladium(0)/tri-tert-butylphosphine tetrafluoroborate catalyst system, potassium bicarbonate as the base and a solvent consisting of pure water containing a small amount of polyoxyethylene-α-tocopheryl

  通过使用三（二亚苄基丙酮）二钯（0）/三叔丁基膦四氟硼酸酯催化剂体系，碳酸氢钾溶液，以令人满意的产率进行了4-铬酮，酮和2-苯基乙醛与芳基卤化物的高选择性直接CHα-单芳基化反应。作为碱和由纯水组成的溶剂，其中含有少量的聚氧乙烯-α-生育酚癸二酸酯（PTS）。在串联过程中采用了相似的反应条件，从而由羰基化合物和2-溴苯甲酸甲酯生成了苯基取代的异香豆素。