(3S,12bR)-3-phenyl-5-(p-tolyl)-3,12b-dihydro-2H-benzo[b]oxazolo[2,3-f][1,6]naphthyridine | 1533409-56-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: (3S,12bR)-3-phenyl-5-(p-tolyl)-3,12b-dihydro-2H-benzo[b]oxazolo[2,3-f][1,6]naphthyridine
• 英文别名: (11R,14S)-16-(4-methylphenyl)-14-phenyl-12-oxa-2,15-diazatetracyclo[8.7.0.03,8.011,15]heptadeca-1,3,5,7,9,16-hexaene
• CAS: 1533409-56-1
• 化学式: C₂₇H₂₂N₂O
• 分子量: 390.484
• InChiKey: WIUAQGAKYHBZRY-KAYWLYCHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  30
• 可旋转键数：
  2
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  25.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  4-甲苯基乙炔 在 gold(III) chloride 作用下， 以 1,2-二氯乙烷 为溶剂， 生成 (3S,12bR)-3-phenyl-5-(p-tolyl)-3,12b-dihydro-2H-benzo[b]oxazolo[2,3-f][1,6]naphthyridine
  参考文献：
  名称：

  Au(III)-catalyzed regio- and stereoselective tandem synthesis of oxazolo fused naphthyridines and isoquinolines from o-alkynylaldehydes

  摘要：

  An efficient tandem approach for the regio- and stereoselective synthesis of oxazolo-fused naphthyridines 3a-g, 3i-l and isoquinolines 3h, 3m via the reaction of o-alkynylaldehydes 1a-i with chiral amino alcohols 2a-c under mild reaction conditions is described. The stereochemistry and structures of the products were assigned via NOESY and X-ray crystallographic studies. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2013.11.072

文献信息

• Au(III)-catalyzed regio- and stereoselective tandem synthesis of oxazolo fused naphthyridines and isoquinolines from o-alkynylaldehydes
  作者：Rajeev Ranjan Jha、Abhinandan Kumar Danodia、Sushil Kumar、Akhilesh Kumar Verma

  DOI：10.1016/j.tetlet.2013.11.072

  日期：2014.1

  An efficient tandem approach for the regio- and stereoselective synthesis of oxazolo-fused naphthyridines 3a-g, 3i-l and isoquinolines 3h, 3m via the reaction of o-alkynylaldehydes 1a-i with chiral amino alcohols 2a-c under mild reaction conditions is described. The stereochemistry and structures of the products were assigned via NOESY and X-ray crystallographic studies. (C) 2013 Elsevier Ltd. All rights reserved.