One-Pot Tandem 1,3-Dipolar Cycloaddition of Azinium Ylides Using Water as Solvent

Author(s): Deepika Singh, Pragya Sinha, Raj K. Bansal

Journal Name: Current Green Chemistry

Volume 1 , Issue 3 , 2014

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Graphical Abstract:


Following an important principle of Green Chemistry, namely the use of a benign solvent, the reaction of azines, namely pyridine, isoquinoline and phenanthridine with phenacyl bromides or with t-butyl bromoacetate has been accomplished in water to generate an aqueous solution of the (substituted methyl)azinium bromides, which on further reacting with dimethyl acetylenedicarboxylate (DMAD) and potassium carbonate furnish annelated pyrroles through tandem formation of the azinium methylides followed by 1,3-dipolar cycloaddition. In one case, maleic anhydride could also be used as 1,3-dipolarophile. The products are obtained in good yields and have been well characterized.

Keywords: Azinium ylides, 1, 3-Dipolar cycloaddition, DMAD, maleic anhydride, pyrrolo[1, 2-f]phenanthridines, water as solvent.

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Article Details

Year: 2014
Published on: 02 September, 2014
Page: [227 - 231]
Pages: 5
DOI: 10.2174/2213346101666140210194354
Price: $25

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