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Synthesis of New 8-Formyl-4-methyl-7-hydroxy Coumarin Derivatives
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 Title & Authors
Synthesis of New 8-Formyl-4-methyl-7-hydroxy Coumarin Derivatives
Manidhar, D.M.; Rao, K. Uma Maheswara; Reddy, N. Bakthavatchala; Sundar, Ch. Syama; Reddy, C. Suresh;
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 Abstract
8-Formyl-4-Methyl-7-Hydroxy Coumarin Derivatives were synthesized via Penchem condensation followed by Duffs reaction. Treatment of this with N,N-di substituted cyano acetamides in the presence of piperdine afforded New 8-Formyl-4-Methyl-7-Hydroxy Coumarin Derivatives (7a-o). Their structures were characterized by IR, and NMR and Mass spectral and elemental analysis data.
 Keywords
N,N-di substituted cyano acetamides;Piperdine;Coumarin derivatives;
 Language
English
 Cited by
1.
Synthesis of novel 2H,8H-pyrano[2,3-f]chromene-2,8-diones from 8-formyl-7-hydroxy-4-methylcoumarin, Tetrahedron Letters, 2013, 54, 37, 5111  crossref(new windwow)
2.
Synthesis, Characterization, Photophysical and DFT Studies of Coumarin Schiff Bases and Their Dimethylgallium Complexes, Proceedings of the National Academy of Sciences, India Section A: Physical Sciences, 2016, 86, 4, 633  crossref(new windwow)
3.
Elucidation of the Binding Mechanism of Coumarin Derivatives with Human Serum Albumin, PLoS ONE, 2013, 8, 5, e63805  crossref(new windwow)
4.
Heteroleptic iridium(iii) complexes bearing a coumarin moiety: an experimental and theoretical investigation, RSC Adv., 2015, 5, 96, 78852  crossref(new windwow)
 References
1.
Madhavi, D.; Pushpa, P.; Mary, J.; Usha, P.; Rajashree, K.; Nirmala, D. Indian J. Exp. Biol. 2008, 46, 788.

2.
Mulwad, V. V.; Shirodkar, J. M. Ind. J. Heterocycl. Chem. 2002, 11, 192.

3.
Manohar, K.; Manjunath, G.; Raviraj, K. Indian J. Heterocycl. Chem. 2004, 14, 201.

4.
Rajeshwarrao, V.; Srimanth, K.; Vijayakumar, P. Indian J. Heterocycl. Chem. 2004, 14, 141.

5.
Nofal, Z. M.; El-Zahar, M. I.; Abd, El-Karin, S. S. J. Antimicrob. Chemother. 2005, 5, 483.

6.
Bhattacharyya, S. S.; Paul, S.; Mandal, K. S.; Antara, B.; Naoual, B.; Anisur, R. K.-B. Eur. J. Phram. 2009, 614, 128. crossref(new window)

7.
Pechmann, H.; Duisberg, C. Ber. Dtsch. Chem. Ges. 1883, 16, 2119. crossref(new window)

8.
Patel, A. D.; Sharma, M. S.; Vohra, J. J.; Joshi, J. D. J. Indian Chem. Soc. 1997, 74, 287.

9.
Wang, K.; Nguyen, K.; Huang, Y.; Domling, A. Journal of Combinatorial Chemistry 2009, 11, 920. crossref(new window)

10.
Tamiz, A. P.; Cai, S. X.; Zhou, Z. L.; Yuen, P. W.; Schelkun, R. M.; Whittemore, E. R.; Weber, E.; Woodward, R. M.; Keana, J. F. W. J. Med. Chem. 1999, 42, 3412. crossref(new window)

11.
McChuskey, A.; Robinson, P. J.; Hill, T.; Scott, J. L.; Edwards, J. K. Tettrahedron Lett. 2002, 43, 3117. crossref(new window)