Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9317
Title: A catalyst-free, efficient green MCR protocol for access to functionalized γ-carbolines in water
Authors: Biswas, Soumen
Samanta, Sampak
Keywords: Polycyclic aromatic hydrocarbons;Ammonium acetate;Annulation reactions;Carboline derivatives;Functionalized;Important features;Indole derivatives;Room temperature;Three component reactions;Catalysts
Issue Date: 2015
Publisher: Royal Society of Chemistry
Citation: Dagar, A., Biswas, S., & Samanta, S. (2015). A catalyst-free, efficient green MCR protocol for access to functionalized γ-carbolines in water. RSC Advances, 5(65), 52497-52507. doi:10.1039/c5ra08422a
Abstract: A general, mild, efficient and practical approach for the construction of functionalized γ-carboline derivatives has been successfully realized in water through a one-pot three-component reaction involving several aryl/hetero-aryl/alkyl/alkenyl/alkynyl/ferrocenyl aldehydes, 3-formyl indole derivatives and ammonium acetate as a cheap N-source. The most important feature of the current methodology is that this hetero-annulation reaction of indole to γ-carboline can occur in good to excellent yields with wider substrate scope at room temperature in water, starting from simple inexpensive raw materials under catalyst-free and oxidant-free conditions. Moreover, a facile access to pentacyclic quinolinone fused carboline derivative has been achieved through our methodology. © The Royal Society of Chemistry.
URI: https://doi.org/10.1039/c5ra08422a
https://dspace.iiti.ac.in/handle/123456789/9317
ISSN: 2046-2069
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

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