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

Issue cover





  Open Access OPEN ACCESS | Open Access PEER-REVIEWED | SHORT COMMUNICATION | DOWNLOAD PDF | VIEW FULL-TEXT PDF | TOTAL VIEWS

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).


Announcements


Our editors have decided to support scientists to publish their manuscripts in European Journal of Chemistry without any financial constraints.

1- The article processing fee will not be charged from the articles containing the single-crystal structure characterization between November 15, 2022 and December 28, 2022 (Voucher code: SINGLE2022).

2. Young writers will not be charged for the article processing fee between November 15, 2022 and December 28, 2022 (Voucher code: YOUNG2022).

3. The article processing fee will not be charged from the articles containing a part of the PhD thesis between November 15, 2022 and December 28, 2022 (Voucher code: PhD2022).

4. The article processing fee will not be charged from authors who have at least one publication in the European Journal of Chemistry between November 15, 2022 and December 28, 2022 (Voucher code: (Voucher code: AUTHOR2022).

Editor-in-Chief

European Journal of Chemistry

Keywords


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

Full Text:

PDF
PDF    Open Access

DOI: 10.5155/eurjchem.5.4.668-670.1085

Links for Article


| | | | | |

| | | | | | |

| | | |

Related Articles




Article Metrics

icon graph This Abstract was viewed 895 times | icon graph PDF Article downloaded 480 times

Funding information


Council of Scientific and Industrial Research, New Delhi, India

Citations

/


[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
/


[2]. Lenida Kyndiah, Fillip Kumar Sarkar, Ajay Gupta, Amarta Kumar Pal
Efficient metal-free green syntheses of 4H-chromenes and 3-amino alkylated indoles using a reusable graphite oxide carbocatalyst under aqueous and solvent-free reaction conditions
New Journal of Chemistry  46(24), 11706, 2022
DOI: 10.1039/D2NJ00756H
/


[3]. 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
/


[4]. 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
/


[5]. 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
/


[6]. 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
/


References


[1]. Domling, A. Chem. Rev. 2006, 106, 17-89.
http://dx.doi.org/10.1021/cr0505728

[2]. Tejedor, D.; Cruz, D. G.; Exposito, A. S.; Tellado, J. J. M.; Armas, P. D.; Tellado, F. G. Chem. Eur. J. 2005, 11, 3502-3510.
http://dx.doi.org/10.1002/chem.200401267

[3]. Ramon, D. J.; Yus, M. Angew. Chem. Int. Ed. 2005, 44, 1602-1634.
http://dx.doi.org/10.1002/anie.200460548

[4]. Simon, C.; Constantieux, T.; Rodriguez, J. Org. Chem. 2004, 24, 4957-4980.

[5]. Orru, R. V. A.; Michiel, D. G. Synthesis 2003, 1471-1499.
http://dx.doi.org/10.1055/s-2003-40507

[6]. Bienayme, H.; Hulme, C.; Oddon, G.; Schmitt, P. Chem. Eur. J. 2000, 6, 3321-3329.
http://dx.doi.org/10.1002/1521-3765(20000915)6:18<3321::AID-CHEM3321>3.0.CO;2-A

[7]. Ulaczyk-Lesanko, A.; Hall, D. G. Current Chem. Biol. 2005, 9, 266-276.

[8]. Weber, L. Curr. Med. Chem. 2002, 9, 2085-2093.
http://dx.doi.org/10.2174/0929867023368719

[9]. Hulme, H.; Gore, V. Curr. Med. Chem. 2003, 10, 51-80.
http://dx.doi.org/10.2174/0929867033368600

[10]. Jiang, B.; Yang, C. G.; Wang, J. J. Org. Chem. 2001, 66, 4865-4869.
http://dx.doi.org/10.1021/jo010265b

[11]. Leze, M. P.; Le Borgne, M.; Marchand, P.; Loquet, D.; Kogler, M.; Le Baut, G.; Palusczak, A.; Hartmann, R. W. J. Med. Chem. 2004, 19, 549-557.

[12]. Deng, J.; Sanchez, T.; Neamati, N.; Briggs, J. M. J. Med. Chem. 2006, 49, 1684-1692.
http://dx.doi.org/10.1021/jm0510629

[13]. Wynne, J. H.; Stalick, W. M. J. Org. Chem. 2002, 67, 5850-5853.
http://dx.doi.org/10.1021/jo020049i

[14]. Sundberg, R. J. Indoles, Academic Press, San Diego, 1996.

[15]. Shankar, J.; Karnakar, K.; Srinivas, B.; Nageswar, Y. V. D. Tetrahedron Lett. 2010, 51, 3938-3939.
http://dx.doi.org/10.1016/j.tetlet.2010.05.096

[16]. Ramesh, K.; Murthy, S. N.; Karnakar. K.; Nageswar, Y. V. D. Tetrahedron Lett. 2011, 52, 4734-4737.
http://dx.doi.org/10.1016/j.tetlet.2011.06.098

[17]. Ramesh, K.; Murthy, S. N.; Nageswar, Y. V. D. Tetrahedron Lett. 2011, 52, 2362-2366.
http://dx.doi.org/10.1016/j.tetlet.2011.02.082

[18]. Ramesh, K.; Murthy, S. N.; Karnakar. K.; Nageswar, Y. V. D. Tetrahedron Lett. 2011, 52, 3937-3941.
http://dx.doi.org/10.1016/j.tetlet.2011.05.100

[19]. Ramesh, K.; Karnakar, K.; Satish, G.; Reddy, K. H. V.; Nageswar, Y. V. D. Tetrahedron Lett. 2012, 53, 6095-6099.
http://dx.doi.org/10.1016/j.tetlet.2012.08.141

[20]. Ramesh, K.; Karnakar, K.; Satish, G.; Anil Kumar, B. S. P.; Nageswar, Y. V. D. Tetrahedron Lett. 2012, 53, 6936-6939.
http://dx.doi.org/10.1016/j.tetlet.2012.10.029

[21]. Ramesh, K.; Narayana Murthy, S.; Karnakar, K.; Nageswar, Y. V. D. Eur. J. Chem. 2012, 3(1), 119-124.
http://dx.doi.org/10.5155/eurjchem.3.1.119-124.449

[22]. Swapna, K.; Narayana Murthy, S.; Nageswar, Y. V. D. Eur. J. Chem. 2011. 2(2), 272-275
http://dx.doi.org/10.5155/eurjchem.2.2.272-275.359


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. 28 Nov. 2022
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)

The other citation formats (EndNote | Reference Manager | ProCite | BibTeX | RefWorks) for this article can be found online at: How to cite item



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


CrossRef | Scilit | GrowKudos | Researchgate | Publons | ScienceGate | Scite | Lens | OUCI

WorldCat Paperbuzz | LibKey Citeas | Dimensions | Semanticscholar | Plumx | Kopernio | Zotero | Mendeley

ZoteroSave to Zotero MendeleySave to Mendeley



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

Refbacks

  • There are currently no refbacks.




Copyright (c)





© Copyright 2010 - 2022  Atlanta Publishing House LLC All Right Reserved.

The opinions expressed in all articles published in European Journal of Chemistry are those of the specific author(s), and do not necessarily reflect the views of Atlanta Publishing House LLC, or European Journal of Chemistry, or any of its employees.

Copyright 2010-2022 Atlanta Publishing House LLC. All rights reserved. This site is owned and operated by Atlanta Publishing House LLC whose registered office is 2850 Smith Ridge Trce Peachtree Cor GA 30071-2636, USA. Registered in USA.