Subscribe

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

ILCPA > Volume 29 > Microwave Assisted Synthesis of...
< Back to Volume

Microwave Assisted Synthesis of 2,5-Distyryl-1,3,4-Oxadiazole Derivatives as Anti Microbial Agents

Full Text PDF

Abstract:

A new series of 2,5-distyryl-1,3,4-oxadiazoles derivatives have been synthesized from cinnamic hydrazide on reaction with various cinnamic acid derivatives. The structures of synthesized compounds have been elucidated by spectral studies like IR, 1HNMR, Mass and also Elemental Analysis. Furthermore, all synthesized compounds were screened for In Vitro anti microbial activity against the gram positive (Staphylococcus aureus, Pseudomonas aeruginosa) and gram negative (Escherichia coli) bacterial strain. In which some the compounds show potential inhibition against the test organisms.

Info:

Periodical:
International Letters of Chemistry, Physics and Astronomy (Volume 29)
Pages:
46-54
Citation:
D. L. Namera et al., "Microwave Assisted Synthesis of 2,5-Distyryl-1,3,4-Oxadiazole Derivatives as Anti Microbial Agents", International Letters of Chemistry, Physics and Astronomy, Vol. 29, pp. 46-54, 2014
Online since:
March 2014
Export:
Distribution:
References:

S. Chao, X. Li, S. Wang, Huaxue Yanjiu Yu Yingyong. 22(8) (2010) 1066-1071.

B. Chandrakantha, Prakash Shetty, Vijesh Nambiyar, Nishitha Isloor, Arun M. Isloor, European Journal of Medicinal Chemistry 45 (2010) 1206-1210.

Rakesh Kumar, M. Shahar Yar, A. K. Rail, Saurabh Chaturvedi, Der Pharmacia Lettre 5 (1) (2013) 366-370.

N. Jain, D. P. Pathak, P. Mishra, S. Jain, J. Iranian Chem. Soc. 6 (2009) 77.

L. Srikanth, U. Naik, R. Jadhav, N. Raghunandan, J. Rao, K. Manohar., Pharma Chemica 2(4) (2010) 231-243.

M. Bhat, M. Al-Omar, N. Siddiqui, Pharma Chemica 2(2) (2010) 1-10.

K. Sushil, V. Gupta, V. Kashaw, P. Mishra, J. Stables, N. Jain., Med. Chem. Research. 38(2) (2009) 157-159.

L. Jin, J. Chen, B. Song, Z. Chen, S. Yang, Q. Li, D. Hu, R. Xu, Bioorg. Med. Chem. Lett. 16 (2006) 5036.

Wang Bao-Lei, Li Zheng-Ming, Li Yong-Hong, Wang Su-Hua, Gaodeng Xuexia o Huaxue Xuebao 29(1) (2008) 90-94.

C. R. W. Guimaraes, D. L. Boger, W. L. Jorgensen, J. Am. Chem. Soc. 127 (2005) 17377-17384.

B. Narayana, B. V. Ashalatha, a K. K. Vijaya Raj, J. Fernandes and B. K. Sarojini, Bioorganic & Medicinal Chemistry 13 (2005) 4638-4644.

Prateek Sharma, J. Chem. Pharm. Res. 3(2) (2005) 403-423.

Rolando F. Pellon, Taimirys Mamposo, Erick Godlez, Osmar Calderon, Synthetic Communications 30(20) (2000) 3769-3774.

Yin Luo, Ke-Ming Qiu, Xiang Lu, Kai Liu, Jie Fu, Hai-Liang Zhu, Bioorganic & Medicinal Chemistry 19(16) (2011) 4730-4738.

Lei Liu, W. Robert Hudgins, Sonsoles Shack, Mu Quan Yin, Dvorit Samid, International Journal of Cancer 62(3) (1995) 345-350.

Fausta Natella, Mirella Nardini, Maurizio Di Felice, Cristina Scaccini, J. Agric. Food Chem. 47(4) (1999) 1453-1459.

Mario Foti, Mario Piattelli, Maria Tiziana Baratta, Giuseppe Ruberto, J. Agric. Food Chem. 44(2) (1996) 497-501.

Kudelko A., Zieliński W., Tetrahedron Lett. 53 (2012) 76-77.

Rahul R. Tripathi, Ratnamala P. Sonawane, International Letters of Chemistry, Physics and Astronomy 10(2) (2013) 119-125.

Mallikarjun S. Yadawe, Shrishila N. Unki, Sangamesh A. Patil, International Letters of Chemistry, Physics and Astronomy 12 (2013) 94-104.

G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 5 (2014) 89-98.

V. J. Faldu, P. K. Talpara, N. H. Bhuva, P. R. Vachharajani, V. H. Shah, International Letters of Chemistry, Physics and Astronomy 6 (2014) 26-32.

Piyush B. Vekariya, Jalpa R. Pandya, Vaishali Goswami, Hitendra S. Joshi, International Letters of Chemistry, Physics and Astronomy 7 (2014) 45-52.

R. G. Vaghasiya, H. B. Ghodasara, P. R. Vachharajani, V. H. Shah, International Letters of Chemistry, Physics and Astronomy 8 (2014) 30-37. ( Received 21 February 2014; accepted 26 February 2014 ).

Show More Hide