Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 47, 2017 - Issue 21
273
Views
8
CrossRef citations to date
0
Altmetric
Original Articles

CAN-catalyzed microwave promoted reaction of indole with Betti bases under solvent-free condition and evaluation of antibacterial activity of the products

, , , , &
Pages 2007-2014 | Received 26 May 2017, Published online: 05 Oct 2017

References

  • Ho, T. L. Synthesis 1973, 347.
  • Sridharan, V.; Menendez, J. C. Chem. Rev. 2010, 110, 3805–3849.
  • (a) Jang, H.-Y.; Hong, J.-B.; MacMillan, D. W. C. J. Am. Chem. Soc. 2007, 129, 7004; (b) Nair, V.; Mathew, J.; Prabhakaran, J. Chem. Soc. Rev. 1997, 26, 127.
  • (a) Alvarez-Manzaneda, E. J.; Chabouna, R.; Alvarez, E.; Cabrera, E.; Alvarez-Manzaneda, R.; Haidour, A.; Ramos, J. M. Synlett 2006, 1756; (b) Nair, V.; Augustine, A.; Suja, T. D. Synthesis 2002, 2259; (c) Maiti, S.; Menéndez, J. C. Synlett 2009, 2249; (d) Varala, R.; Sreelatha, N.; Adapa, S. R. Synlett 2006, 1549; (e) Nair, V.; Rajan, R.; Rath, N. P. Org. Lett. 2002, 4, 1575.
  • Prajapati, N. P.; Vekariya, R. H.; Patel, H. D. Synth. Commun. 2015, 45, 2399.
  • (a) de la Hoz, A.; Loupy, A. (Eds.) Microwaves in Organic Synthesis, 3rd ed.; Wiley-VCH: Weinheim, 2012; (b) Sanghi, R.; Singh, V. (Eds.) Green Chemistry for Environmental Remediation; Wiley: Hoboken, 2012; (c) Pollastri, M. P.; Devine, W. G. Microwave Synthesis. In Green Techniques for Organic Synthesis and Medicinal Chemistry; Zhang, W., Cue, B. Eds.; Wiley: Chichester, 2012; Ch. 12, pp. 325–342; (d) Tierney, J. P.; Lidstrom, P. (Eds.) Microwave Assisted Organic Synthesis; Blackwell Publishing Ltd: Oxford, 2009; (e) Leadbeater, N. E. Organic Synthesis Using Microwave Heating. In Comprehensive Organic Synthesis, 2nd ed.; Knochel, P., Molander, G. Eds.; Elsevier Ltd: Oxford, 2014; Ch. 10, Vol. 9, pp. 234–286; (f) Kappe, C. O.; Stadler, A. Microwaves in Organic and Medicinal Chemistry, 2nd ed.; Wiley: Weinheim, 2012.
  • (a) Baig, R. B. N.; Varma, R. S. Chem. Soc. Rev. 2012, 41, 1559; (b) Pedersen, S. L.; Tofteng, A. P.; Malik, L.; Jensen, K. J. Chem. Soc. Rev. 2012, 41, 1826; (c) Takkellapati, S. R. Curr. Org. Chem. 2013, 17, 2305; (d) Kappe, C. O. Chem. Soc. Rev. 2013, 42, 4977.
  • (a) Sundberg, R. J. The Chemistry of Indoles; Academic Press: New York, 1996; (b) Juwarker, H.; Suk, J.-M.; Jeong, K.-S. Top. Heterocycl. Chem. 2010, 24, 177; (c) Barluenga, J.; Valdes, C. Five Membered Heterocycles: Indole and Related Systems in Modern Heterocyclic Chemistry; Wiley: New York, 2011; Vol. 1, pp. 377–513; (d) Vicente, R. Org. Biomol. Chem. 2011, 9, 6469; (e) Sharma, V.; Kumar, P.; Pathak, P. J. Heterocycl. Chem. 2010, 47, 491.
  • (a) Kaniwa, K.; Arai, M. A.; Li, X.; Ishibashi, M. Bioorg. Med. Chem. Lett. 2007, 17, 4254 (b) Teng, M.; Zi, W.; Ma, D. Angew. Chem. Int. Ed. 2014, 53, 1814.
  • (a) Basha, A. R. Indole Alkaloids; Harwood Academic: Chichester, UK, 1998; (b) Higuchi, K.; Kawasaki, T. Nat. Prod. Rep. 2007, 24, 843; (c) Ishikura, M.; Yamada, K.; Abe, T. Nat. Prod. Rep. 2010, 27, 1630; (d) Ishikura, M.; Yamada, K. Nat. Prod. Rep. 2009, 26, 803; (e) Somei, M.; Yamada, F. Nat. Prod. Rep. 2005, 22, 73; (f) Walsh, T. F.; Toupence, R. B.; Ujjainwalla, F.; Young, J. R.; Goulet, M. T. Tetrahedron 2001, 57, 5233; (g) Jacotot, B.; Banga, J. D.; Pfister, P.; Mehra, M. Br. J. Clin. Pharmacol. 1994, 38, 257; (h) Reddy, B. V. S.; Reddy, M. R.; Madan, C.; Kumar, K. P.; Rao, M. S. Bioorg. Med. Chem. Lett. 2010, 20, 7507; (i) Chavan, R. S.; More, H. N. J. Pharm. Res. 2011, 4, 1575.
  • (a) Lakshmi, N. V.; Thirumurugan, P.; Noorulla, K. M.; Perumal, P. T. Bioorg. Med. Chem. Lett. 2010, 20, 5054; (b) Biradar, J. S.; Sasidhar, B. S.; Parveen, R. Eur. J. Med. Chem. 2010, 45, 4074; (c) Biradar, J. S.; Sasidhar, B. S. Eur. J. Med. Chem. 2011, 46, 6112; (d) Samadi, A.; Soriano, E.; Revuelta, J.; Valderas, C.; Chioua, M.; Garrido, I.; Bartolomé, B.; Tomassolli, I.; Ismaili, L.; Gonzalez-Lafuente, L.; Villarroya, M.; García, A. G.; Oset-Gasque, M. J.; Marco-Contelles, J. Bioorg. Med. Chem. 2011, 19, 951.
  • (a) Yılmaz, A. D.; Coban, T.; Suzen, S. J. Enzyme Inhib. Med. Chem. 2012, 27, 428; (b) Silveira, C. C.; Mendes, S. R.; Soares, J. R.; Victoria, F. N.; Martinez, D. M.; Savegnago, L. Tetrahedron Lett. 2013, 54, 4926–4929.
  • (a) Manosroi, A.; Jantrawut, P.; Ogihara, E.; Yamamotob, A.; Fukatsu, M.; Yasukawa, K.; Tokuda, H.; Suzuki, N.; Manosroi, J.; Akihisa, T. Chem. Biodiervs. 2013, 10, 1448; (b) Wink, M. Theor. Appl. Genet. 1988, 75, 225.
  • Huang, W.-Y.; Cai, Y.-Z.; Zhang, Y. Nutr. Cancer 2010, 62, 1.
  • (a) Sakihama, Y.; Mano, J.; Sano, S.; Asada, K.; Yamasaki, H. Biochem. Biophys. Res. Commun. 2000, 279, 949; (b) Arora, A.; Nair, M. G.; Strasburg, G. M. Free Radical Biol. Med. 1998, 24, 1355; (c) Evans, C. R.; Miller, N.; Paganga, G. Trends Plant Sci. 1997, 2, 152.
  • Deb, M. L.; Das, C.; Deka, B.; Saikia, P. J.; Baruah, P. K. Synlett 2016, 27, 2788.
  • Deb, M. L.; Saikia, B-S.; Borah, K.; Baruah, P. K. Synth. Commun. 2016, 46, 1940.
  • Deb, M. L.; Pegu, C. D.; Deka, B.; Dutta, P.; Kotmale, A. S.; Baruah, P. K. Eur. J. Org. Chem. 2016, 3441.
  • Sen, A.; Batra, A. Int. J. Curr. Pharm. Res. 2012, 4, 67.
  • Sarker, S. D.; Nahar, L.; Kumarasamy, Y. Methods 2007, 42, 321.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.