Efficient Synthesis of Pyrrolo[1,2-f]phenanthridine Derivatives via Dipolar Cycloaddition of Phenanthridine, Activated Acetylenes, and Ethyl Bromopyruvate

Author： Mehrabi Hossein   Pishahang Jaleh  

Publisher： Taylor & Francis Ltd

ISSN： 0039-7911

Source： Synthetic Communications, Vol.44, Iss.1, 2014-01, pp. : 76-81

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Synthesis of Functionalized Pyrido[1,2-f]phenanthridines from Phenanthridine, Activated Acetylenes, and Arylidenemalononitriles

By Mehrabi Hossein   Hatami-pour Mahdi  

Synthetic Communications, Vol. 43, Iss. 4, 2013-01 ,pp. : 611-618

Taylor & Francis Ltd

Access to resources Recommend Favorite

Synthesis of polyfluorophenyl substituted-4,5-dihydropyrazole derivatives via 1,3-dipolar cycloaddition of nitrile imine with ethyl acrylate

By Song L.-P.   Zhu S.-Z.  

Journal of Fluorine Chemistry, Vol. 124, Iss. 2, 2003-12 ,pp. : 211-217

Elsevier

Access to resources Recommend Favorite

An Efficient Synthesis of Novel Dispirooxindole Derivatives via One-Pot Three-Component 1,3-Dipolar Cycloaddition Reactions

By Huang Zhibin   Zhao Qian   Chen Gang   Wang Huiyuan   Lin Wei   Xu Lexing   Liu Hongtao   Wang Juxian   Shi Daqing   Wang Yucheng  

Molecules, Vol. 17, Iss. 11, 2012-10 ,pp. : 12704-12717

MDPI

Access to resources Recommend Favorite

Dipolar Cycloaddition Reactions with Quinazolinones: A New Route for the Synthesis of Several Annelated Pyrrolo- and Pyridazinoquinazoline Derivatives

By Ghabrial Sami S.   Gaber Hatem M.  

Molecules, Vol. 8, Iss. 5, 2003-05 ,pp. : 401-410

MDPI

Access to resources Recommend Favorite

Stereospecificity of Diels-Alder Reactions Validated Using Ab Initio Calculations: Synthesis of Novel Coumarin and Phenanthridine Derivatives

By El-Shafei A.   Fadda A. A.   Abdel-Gawad I. I.   Youssif E. H. E.  

Synthetic Communications, Vol. 39, Iss. 16, 2009-01 ,pp. : 2954-2972

Taylor & Francis Ltd

Access to resources Recommend Favorite