European Journal of Chemistry 2014, 5(4), 668-670 | doi: https://doi.org/10.5155/eurjchem.5.4.668-670.1085 | Get rights and content






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β-Cyclodextrin catalyzed synthesis of substituted indoles in aqueous medium


Jilla Shankar (1) , Gaddam Satish (2) , Bandam Santosh Pavan Anil Kumar (3) , Yadavalli Venkata Durga Nageswar (4,*)

(1) Council of Scientific Industrial Research-Medicinal Chemistry and Pharmacology Division, Indian Institute of Chemical Technology, Uppal Road, Hyderabad 500-007, India
(2) Council of Scientific Industrial Research-Medicinal Chemistry and Pharmacology Division, Indian Institute of Chemical Technology, Uppal Road, Hyderabad 500-007, India
(3) Council of Scientific Industrial Research-Medicinal Chemistry and Pharmacology Division, Indian Institute of Chemical Technology, Uppal Road, Hyderabad 500-007, India
(4) Council of Scientific Industrial Research-Medicinal Chemistry and Pharmacology Division, Indian Institute of Chemical Technology, Uppal Road, Hyderabad 500-007, India
(*) Corresponding Author

Received: 28 Apr 2014 | Revised: 27 Jun 2014 | Accepted: 16 Jun 2014 | Published: 31 Dec 2014 | Issue Date: December 2014

Abstract


β-Cyclodextrin catalyzed synthesis of indole derivatives from indole, aldehyde and N-methylaniline is reported. The β-cyclodextrin can be recovered and reused without significant loss of catalytic activity, and it is inexpensive, readily available when compared to other cyclodextrins (α, γ).


Keywords


Indole; β-Cyclodextrin; N-Methylaniline; Aqueous medium; N-Methylbenzamines; Aldehyde derivatives

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DOI: 10.5155/eurjchem.5.4.668-670.1085

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Funding information


Council of Scientific and Industrial Research, New Delhi, India

Citations

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[1]. Elisa Bonandi, Dario Perdicchia, Eleonora Colombo, Francesca Foschi, Paola Marzullo, Daniele Passarella
Catalytic C3 aza-alkylation of indoles
Organic & Biomolecular Chemistry  18(32), 6211, 2020
DOI: 10.1039/D0OB01094D
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[2]. Sihai Chen, Jinyang Chen, Xinhua Xu, Yunhua He, Rongnan Yi, Renhua Qiu
Calix[4]arene-assisted KOH-catalyzed synthesis of O,O-dialkyl-Se-aryl phosphoroselenoates
Journal of Organometallic Chemistry  818, 123, 2016
DOI: 10.1016/j.jorganchem.2016.06.010
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[3]. Mohsen Abbasi
β-Cyclodextrin as an Efficient and Recyclable Supramolecular Catalyst for the Synthesis of Heterocyclic Compounds
Journal of the Chinese Chemical Society  64(8), 896, 2017
DOI: 10.1002/jccs.201600887
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[4]. Giovanna Bosica, Roderick Abdilla
A regioselective one-pot aza-Friedel–Crafts reaction for primary, secondary and tertiary anilines using a heterogeneous catalyst
Green Chemistry  19(23), 5683, 2017
DOI: 10.1039/C7GC02038D
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[5]. Alevtina S. Medvedeva, Maria M. Demina, Tran D. Vu, Mikhail V. Andreev, Nina S. Shaglaeva, Lyudmila I. Larina
β-Cyclodextrin-catalyzed three-component synthesis of 4,5-disubstituted 1,2,3-(NH)-triazoles from propynals, trimethylsilyl azide and malononitrile in water
Mendeleev Communications  26(4), 326, 2016
DOI: 10.1016/j.mencom.2016.07.020
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How to cite


Shankar, J.; Satish, G.; Kumar, B.; Nageswar, Y. Eur. J. Chem. 2014, 5(4), 668-670. doi:10.5155/eurjchem.5.4.668-670.1085
Shankar, J.; Satish, G.; Kumar, B.; Nageswar, Y. β-Cyclodextrin catalyzed synthesis of substituted indoles in aqueous medium. Eur. J. Chem. 2014, 5(4), 668-670. doi:10.5155/eurjchem.5.4.668-670.1085
Shankar, J., Satish, G., Kumar, B., & Nageswar, Y. (2014). β-Cyclodextrin catalyzed synthesis of substituted indoles in aqueous medium. European Journal of Chemistry, 5(4), 668-670. doi:10.5155/eurjchem.5.4.668-670.1085
Shankar, Jilla, Gaddam Satish, Bandam Santosh Pavan Anil Kumar, & Yadavalli Venkata Durga Nageswar. "β-Cyclodextrin catalyzed synthesis of substituted indoles in aqueous medium." European Journal of Chemistry [Online], 5.4 (2014): 668-670. Web. 5 Dec. 2020
Shankar, Jilla, Satish, Gaddam, Kumar, Bandam, AND Nageswar, Yadavalli. "β-Cyclodextrin catalyzed synthesis of substituted indoles in aqueous medium" European Journal of Chemistry [Online], Volume 5 Number 4 (31 December 2014)

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DOI Link: https://doi.org/10.5155/eurjchem.5.4.668-670.1085

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