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Efficient CAN catalyzed synthesis of 1H-indazolo[1,2-b] phthalazine-1,6,11-triones:An eco-friendly protocol 被引量:3

Efficient CAN catalyzed synthesis of 1H-indazolo[1,2-b] phthalazine-1,6,11-triones:An eco-friendly protocol
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摘要 A convenient,economical and green approach to the synthesis of 1H-indazolo[1,2-b]phthalazine-1,6,11-trione derivatives has been achieved via a one-pot protocol using phthalhydrazide,a cyclic-β-diketone and an aldehyde in the presence of a ceric ammonium nitrate catalyst in polyethylene glycol.The simple work up,mild conditions,excellent yields,inexpensive and non-toxic catalyst and simple solvent recyclability render this protocol both attractive and economically viable. A convenient, economical and green approach to the synthesis of 1H-indazolo[1,2-b]phthalazine-1,6,11-trione derivatives has been achieved via a one-pot protocol using phthalhydrazide, a cyclic-β-diketone and an aldehyde in the presence of aceric am- monium nitrate catalyst in polyethylene glycol. The simple work up, mild conditions, excellent yields, inexpensive and non-toxic catalyst and simple solvent recyclability render this protocol both attractive and economically viable.
出处 《Chinese Science Bulletin》 SCIE EI CAS 2012年第18期2273-2279,共7页
关键词 催化合成 协议 生态友好 CAN 邻苯二甲酰 合成方法 酮衍生物 聚乙二醇 ceric ammonium nitrate, polyethylene glycol, 1H-indazolo[1,2-b]phthalazine-1,6,11-triones, recyclability, green chemistry
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  • 1Zhu J, Bienayme H. Multicomponent Reactions. Wiley-VCH: Wein- heim, 2005.
  • 2D/3mling A. Recent developments in isocyanide based multicompo- nent reactions in applied chemistry. Chem Rev, 2006, 106:17-89.
  • 3Ramdn D J, Yus M. Asymmetric multicomponent reactions (AMCRs): The new frontier. Angew Chem Int Ed, 2005, 44: 1602- 1634.
  • 4Simon C, Constantieux T, Rodriguez J. Utilisation of 1,3-dicarbonyl derivatives in multicomponent reactions. Eur J Org Chem, 2004, 4957-4980.
  • 5Orru R V A, de Greef M. Recent advances in solution-phase multi- component methodology for the synthesis of heterocyclic compounds. Synthesis, 2003, 1471-1499.
  • 6Bienayme H, Hulme C, Oddon G, et al. Maximizing synthetic effi- ciency: Multi-component transformations lead the way. Chem Eur J, 2000, 6:3321-3329.
  • 7Ulaczyk-Lesanko A, Hall D G. Wanted: New multicomponent reac- tions for generating libraries of polycyclic natural products. Curr Opin Chem Biol, 2005, 9:266-276.
  • 8Weber L. The application of multi-component reactions in drug dis- covery. Curt Med Chem, 2002, 9:2085-2093.
  • 9Hulme C, Gore V. Multi-component reactions: Emerging chemistry in drug discovery "from xylocain to crixivan". Curr Med Chem, 2003, 10:51-80.
  • 10D6mling A, Ugi I. Multicomponent reactions with isocyanides. An- gew Chem Int Ed, 2000, 39:3168-3210.

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