Paper Titles in Periodical
International Letters of Chemistry, Physics and Astronomy
Volume 30

Subscribe

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

ILCPA > Volume 30 > Synthesis of Benzthiazole Derivatives Grouping...
< Back to Volume

Synthesis of Benzthiazole Derivatives Grouping with Substituted Azetidinone Ring and its Functional Behaviour

Full Text PDF

Abstract:

A series of Schiff derivatives (5a-q) and azetidinone by way of amide linkage analogues (6a-q) containing 2-amino benzthiazole have been synthesized. Amide linkage were adapted from acid via reaction with hydrazine hydrate followed by reaction with different substituted aldehyde derived various Arylidene derivatives comprising with various donor and acceptor functional group. The structures of the new synthesized azetidinone derivatives were characterized on the basis of 1H-NMR, Mass, IR and elemental analysis data.

Info:

Periodical:
International Letters of Chemistry, Physics and Astronomy (Volume 30)
Pages:
223-232
Citation:
K. M. Kapadiya et al., "Synthesis of Benzthiazole Derivatives Grouping with Substituted Azetidinone Ring and its Functional Behaviour", International Letters of Chemistry, Physics and Astronomy, Vol. 30, pp. 223-232, 2014
Online since:
March 2014
Export:
Distribution:
References:

Bradshaw, T. D.; Wrigley, S.; Shi, D. F.; Schulz, R. J.; Paull, K. D.; Stevens, M. F. G. Br., J. Cancer 77(1998) 745.

Pratt, A. J.; Getzoff, E. D.; Perry J. J., Degener. Neurol. Neuromuscul. Dis. (2012) 1-14.

Glicksman, M. A., Expert Opin. Drug Discov. 6 (2011) 1127-1138.

Van Heusden, et al., J. Cancer 86 (2002) 605.

Ali R., Siddiqui N. Journal of Chemistry 2013, Article ID 345198, 12.

Junne S.B., Kadam A. B., Zangade S. B., Shinde S. L. and Vibhute Y. B., International Multidisciplinary Research Journal 6 (2012) 44-47.

Lourenco M.C.S., Souza M.V.N., Pinheiro A.C., Ferreira M.L., Goncalves R.S.B., Nogueira T.C.M., Peraltab M.A., Arkivoc 15 (2007) 181-191.

Navin B. Patel, Jaymin C. Patel, Arabian Journal of Chemistry 4 (2011) 403-411.

S. Sharma, V.K. Srivastava, A. Kumar, Eur. J. Med. Chem. 37 (2002) 689-697.

P. Vicini, M. Incerti, I.A. Doytchinova, P.L. Colla, B. Busonera, R. Loddo,. J. Med. Chem. 41 (2006) 624-632.

J.V. Ragavendran, D. Sriram, S.K. Patel, I.V. Reddy, N. Bharathwajan, J. Stables, P. Yogeeswari, Eur. J. Med. Chem. 42 (2007) 146-151.

Alcaide B, Almendros P., Chem. Soc. Rev. 30 (2001) 226-240.

Rajasekaran, A., Periasamy, M., Venkatesan, S., J Dev Bio and Tiss Eng. 2 (2010) 5.

Pandey, V. K., Gupta, V. D., Upadhyay, M., Singh, V. K., Tandon, M. Ind J Chem. 44 (2005) 158.

Kagthara, P., Teja, S., Rajeev, D., Parekh, H. H., Ind J Hetero Chem. 10 (2000) 9.

Mehta P. D., Sengar N. P. S., Subrahmanyam E. V. S., Satyanarayana D., Ind J Pharm Sci. 68 (2006) 103.

Show More Hide