Subscribe

Subscribe to our Newsletter and get informed about new publication regulary and special discounts for subscribers!

ILCPA > Volume 26 > A Rapid, Convient and Diversified-Multicomponent...
< Back to Volume

A Rapid, Convient and Diversified-Multicomponent Synthesis and Characterization of Pyrano[2,3-b]Indoles

Full Text PDF

Abstract:

A series of pyrano[2,3-b]indoles, was efficiently synthesized via one-pot, multi component reaction (MCRs) of 1,3-bifunctional synthon(malononitrile/ethylcyano acetate), aromatic aldehydes and oxiindole in the presence of various basic catalyst. The key advantages of this process are high yields, shorter reaction times, easy work-up, and purification of products by non-chromatographic method.

Info:

Periodical:
International Letters of Chemistry, Physics and Astronomy (Volume 26)
Pages:
69-76
DOI:
https://doi.org/10.18052/www.scipress.com/ILCPA.26.69
Citation:
H.B. Ghodasara et al., "A Rapid, Convient and Diversified-Multicomponent Synthesis and Characterization of Pyrano[2,3-b]Indoles", International Letters of Chemistry, Physics and Astronomy, Vol. 26, pp. 69-76, 2014
Online since:
Jan 2014
Authors:
H.B. Ghodasara, P.M. Singala, Viresh H. Shah
Keywords:
1,3-Bifunctional Synthon, Multi Component Reaction, Non-Chromatographic Method, Pyrano[2,3-b]Indoles
Export:
RIS, BibTeX, Text
Distribution:
Open Access

Creative Commons License
This work is licensed under a
Creative Commons Attribution 4.0 International License

References:

D. M. D'Souza, T. J. Müller, Chem. Soc. Rev. 36 (2007) 1095.

A. Domling, Chem. Rev. 106 (2006) 17.

I. Ugi, Pure and Appl. Chem. 73 (2001) 187.

F. Lie'by-Muller, C. Simon, T. Constantieux, J. Rodriguez, Comb. Sci. 25 (2006 ) 432.

C. Simon, T. Constantieux, J. Rodriguez, Eur. J. Org. Chem. 24 (2004) 4957.

N. Evdokimov, A. Kireev, A. Yakovenko, M. Antipin, I. Magedov, J. Kornienko, J. Org. Chem. 72 (2007) 3443.

J. L. Wang, D. Liu, Z. J. Zhang, S. Shan, X. Han, S. M. Srinivasula, C. M. Croce, E. S. Alnemri, Z. Huang, Proc. Natl. Acad. Sci. U.S.A. 97 (2000) 7124.

E. S. El-Tamany, F. A. El-Shahed, B. H. Mohamed, J. Serb. Chem. Soc. 64 (1999) 9.

M. E. A. Zaki, H. A. Soliman, O. A. Hiekal, A. E. Rashad, Z. Naturforsch. C. 61c (2006) 1.

F. M. Abdelrazek, P. Metz, N. H. Metwally, S. F. El-Mahrouky, Arch. Pharm. 339 (2006) 456.

F. M. Abdelrazek, P. Metz, O. Kataeva, A. Jager, S. F. EI-Mahrouky, Arch. Pharm. 340 (2007) 543.

N. Foloppe, L. M. Fisher, R. Howes, A. Potter, A. G. S. Robertson, A. E. Surgenor, Bioorg. Med. Chem. 14 (2006) 4792.

V. Y. Sosnovskikh, M. A. Barabanov, B. I. Usachev, R. A. Irgashev, V. S. Moshkin, Russ. Chem. Bull., Int. Ed. 54 (2005) 2846.

H. Junek, H. Aigner, Chem. Ber. 106 (1973) 914.

H. H. Otto, Arch. Pharm. 307 (1974) 444.

Yu. A. Sharanin, L. G. Sharanina, V. V. Puzanova, Zh. Org. Khim. 19 (1983) 2609.

K. Kuppusamy, P. Kasi, Tetrahedron Lett. 51 (2010) 3312.

H. Mecadon, M. R. Rohman, M. Rajbangshi, B. Myrboh, Tetrahedron Lett. 52 (2011) 2523.

J. W. Pavlik, V. Ervithayasuporn, J. C. MacDonald, S. Tantayanon, ARKIVOC 8 (2009) 57.

Ratnamala P. Sonawane, Rahul R. Tripathi, International Letters of Chemistry, Physics and Astronomy 7(1) (2013) 30-36.

Rahul R. Tripathi, Ratnamala P. Sonawane, International Letters of Chemistry, Physics and Astronomy 10(2) (2013) 119-125. ( Received 19 January 2014; accepted 23 January 2014 ).

Show More Hide