Вы находитесь на странице: 1из 3

DAFTAR PUSTAKA

Ahmad, A., Husain, A., & Khan, S. A. 2016. Synthesis, antimicrobial and
antitubercular activities of some novel pyrazoline derivatives. Journal of
Saudi Chemical Society. 20: 577–584.

Ahmed, M.R., Sastry, V.G., Bano, N., Ravichandra, S. & Raghavendra, M. 2011.
Synthesis and cytotoxic, antioxidant activities of new chalcone
derivatives. Rasayan Journal Chem. 2: 289-294.

Ahuja, M. & Sethi, R., 2015. Synthesis and characterization of some novel 2-
pyrazoline derivaties and study of their antibacterial activity. Scientific
Reviews & Chemical Comunication. 5(1): 7–12.
Ajay Kumar, K. & Govindaraju, M. 2015. Pyrazolines: versatile molecules of
synthetic and pharmaceutical applications-a review. International
Journal of ChemTech Research. 8(1): 313–322.

Chemie, W. F., De, D. O., Wirtschaft, S., Chebanov, V. A., Gura, K. A., Desenko,
S. M. 2010. Synthesis of heterocycles via multicomponent reactions I
schnell und portofrei erhältlich bei aminoazoles as key reagents in
multicomponent heterocyclizations. Topics in Heterocyclic Chemistry.
23: 41–48.

Chovatia, Y.S., Gandhi, S. P., Gorde, P. L., Bagade, S.B. 2010. Synthesis and
antimicrobial activity of some pyrazoline derivatives. Oriental Journal of
Chemistry. 26(1): 275–278.
Eftekhari-sis, B., Zirak, M. Akbari, A. 2012. Arylglyoxals in Synthesis of
Heterocyclic Compounds. American Chemical Society.
Hawaiz, F.E., Hussein, A.J. Samad, M.K. 2014. One-pot three component
synthesis of some new azo-pyrazoline derivatives. European Journal of
Chemistry 5(2): 233–236.
Hayashi, Y. 2016. Pot economy and one-pot synthesis. Royal Society of
Chemistry. 1–15.
Hayes, B.L. 2002. Microwave Synthesis: Chemistry at The Speed of Light. CEM
Publishing, New York.
Jadhav, S.B., Shastri, R.A., Gaikwad, K.V. Gaikwad, S.V. 2009. Synthesis and
antimicrobial studies of some novel schiff bases. E-Journal of
Chemistry. 6: 183–188.
Jain, D.K., Bhadoriya, U. Lodhi, J.L. 2013. Synthesis, characterization and
biological evaluation of some new pyrazoline derivatives. Asian Journal
Chemistry. 25(3): 1387–1390.

25
Jasril, J., Zamri, A., Ikhtiarudin, I., Hilwan, Y. 2016. 5-(4-Fluorophenyl)-3-
(naphthalen-1-yl)-1-phenyl-4,5-dihydro-1H-pyrazole. Molbank. 1-5.
Kalsum, U. 2011. Sintesis pirazolin dari kalkon dan uji aktivitasnya sebagai
antimikroba. Skripsi. FMIPA UR, Pekanbaru.
Kappe, C.O., Dallinger, D.&Murphee, S.S. 2009. Practical Microwave Synthesis
for Organic Chemists: Strategies, Instruments and Protocols.
Wiley-VCH, Weinheim. ISBN: 978-3-527-32097-4.
Kharatmol, M.G., Jagdale, D.M., 2017. Eco-friendly synthesis of pyrazoline
derivatives. International Journal of Pharmaceutical and Clinical
Research. 9(4): 302-308
Loh W, Quah C K, Chia T S, Fun H, Sapnakumri M, Narayana B and Sarojini B
K. 2013. Synthesis and crystal structures of n-substituted pyrazolines.
Molecules. 18(2): 2386-2396.
Maleki, A. Ghamari, N. 2013. A three-component one-pot procedure for the
synthesis benzimidazolo- quinazolinone derivatives in the presence of
chitosan-supported metal nanocomposite as a green and reusable catalyst.
Molecules. 17: 1–9.
Manna, K., Banik, U., Ghosh, P. S., Das, M. 2014. A review on synthesis and
pharmacological diversity of isoxazoles & pyrazolines. Journal of
Pharmacy Science. 1(1): 37–49.
Meyer, B.N., Ferrigni, N.R., Putman, J.E., Jacobsen, L.B., Nichols, D.E., &
McLaughiin, J.L. 1982. Brine shrimp: a convencient general bioassay for
active plants consistuent. Journal of Plant Medical. 45: 31-34.
Rahman, A. Siddiqui, A.A. 2010. Review article pyrazoline derivatives : a worthy
insight into the recent advances and potential pharmacological activities.
International Journal of Pharmaceutical Sciences and Drug Research.
2(3): 165–175.
Rajanarendar, E., Venkateshwarlu, P. Krishna, S.R., 2015. One-Pot three
component domino reaction for the synthesis of novel catalyzed by
PTSA — A green chemistry approach. Green and Sustainable Chemistry.
5: 107–114.
Rao, B. M., Ramesh, S., Bardalai, D., Rahman, H., Shaik, H. A. 2013. Synthesis,
characterization and evaluation of anti-epileptic activity of four new 2-
pyrazoline derivatives compounds. Scholars Journal of Applied Medical
Sciences. 1(1): 20–27.
Ravichandran, S. Karthikeyan, E., 2011. Microwave synthesis - A potential tool
for green chemistry. International Journal of ChemTech Research.
3(1): 466–470.

26
Reza, A. I. 2015. Sintesis, karakterisasi dan uji aktivitas antidiabetes senyawa
1,3,5-triaril-2-pirazolin dalam larutan asam asetat di bawah iradiasi
ultrasonik. Seminar Literatur. Universitas Riau, Pekanbaru.
Sakthinathan, S.P., Vanangamudi, G. Thirunarayanan, G. 2012. Synthesis,
spectral studies and antimicrobial activities of some 2-naphthyl
pyrazoline derivatives. Spectrochimica Acta - Part A: Molecular and
Biomolecular Spectroscopy. 95: 693–700.
Sharma, S., Kaur, S., Bansal, T., Gaba, J. 2014. Review on synthesis of bioactive
pyrazoline derivatives. Chemical Science Transactions. 3(3): 861–875.
Silverstein, R.M., Webster, F.X. Kiemle, D.J. 2005. Spectrometric Identification
of Organic Compounds Seventh Edition. John Wiley & Sons, New
Jersey.

Slobodyanyuk, E. Y., Artamonov, O. S., Shishkin, O. V, Mykhailiuk, P. K. 2012.


One-pot synthesis of CF 3 -substituted pyrazolines / pyrazoles from
electron- deficient alkenes / alkynes and CF 3 CHN 2 generated in situ :
optimized synthesis of tris ( trifluoromethyl ) pyrazole. European
Journal of Organic Chemistry. 1: 1–10.

Vaismaa, M. 2009. Development of Benign Synthesis of Some Terminal


-hydroxy Ketone and Aldehydes. Disertasi. Faculty of Science
University of Oulu.

Taj, T. Kamble, R. R., Gireesh, T.M., Hunnur, R. K., Margankop , S. B. 2011.


One-pot synthesis of pyrazoline derivatised carbazoles as antitubercular ,
anticancer agents , their DNA cleavage and antioxidant activities.
European Journal of Medicinal Chemistry. 46(9): 4366–4373.
Toure, B.B. Hall, D.G., 2009. Natural product synthesis using multicomponent
reaction strategies. American Chemical Society. 109: 4439–4486.
Zamri, A., Teruna, H. Y.,&Ikhtiarudin, I. 2016. The Influence of Power Variation
on Selectivity of Synthesis Reaction of 2 ’-hydroxychalcone Analogue
Under Microwave Irradiation. Molekul.11: 299–307.

27

Вам также может понравиться