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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 40, 2010 - Issue 15
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Original Articles

Facile One-Pot Synthesis of Ferrocene-Based Spiropyrrolidines and Pyrrolizidines Through 1,3-Dipolar Cycloaddition Reaction

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Pages 2311-2319 | Received 18 Mar 2009, Published online: 06 Jul 2010

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  • (a) Suresh Babu , A. R. ; Raghunathan , R. Microwave-induced regioselective synthesis of novel dispiro[acenapthenone-indanediones]pyrrolizidines . J. Hetero. Chem. 2006 , 43 , 1357 – 1360 ; (b) Suresh Babu , A. R. ; Raghunathan , R. Synthesis of dispiroheterocyclic framework via the regioselective 1,3-dipolar cycloaddition reaction of azomethine ylides . Synth. Commun. 2007 , 37 , 451 – 458 .
  • (a) Satiskumar , B. K. ; Gayathri , D. ; Velmurugan , D. ; Ravikumar , K. ; Suresh Babu , A. R. 4′-Ferrocenyl-3′-(4-methoxybenzoyl)-1′-methyl-spiro[1H-indole-3(2H), 2′-pyrrolidin]-2-one . Acta. Cryst. 2007 , E63 , m1287 – m1289 ; (b) The crystal structures have been deposited at the Cambridge Crystallographic Data Centre and allocated the deposition numbers CCDC 6756597 for spiro-[2,3′]-5′,7′-dibromooxindole-3-ferrocenoyl-4-furyl-pyrrolizidine and CCDC 292368 for spiro-[2,3′]-oxindole-3-(p-methoxybenzoyl)-4-ferrocenyl-pyrrolizidine .

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