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396. Ausra Voskiene,Vytautas Mickevicius, and Gema Mikulskiene ARKIVOC 2007 (xv)303-314.397. Ranjana Aggarwal and Rajiv Kumar Department of Chemistry,Kurukshetra<strong>University</strong>, Kurukshetra, Haryana, India Synthetic Communications 2009, 39 ,2169–2177398. S. Tripathi ; B. R. Pandey and co-workers ; Indian J. Physical pharmacol. 1980,24(2), 155.399. Zalgislaw K. ; Zbigniew and A. Seffan ; Acta. Pol. Pharma., 1979, 36(6), 645 ;Chem. Abstr., 1980, 93, 204525e.400. Z. Brozozowsk E. Pomarnaka ; Acta. Pol. Pharm., 1980, 37(4), 1378 ; Chem.Abstr., 1981, 25, 80807.401. Ashok kumar, R. S. Verma and B. P. Jagu ; J. Ind. Chem. Soc. 1990, 67, 120.402. D. Bhaskar Reddy, T. Seshama, B. Seehaiha & M. V. Ramma Reddy ; Indian J.Chem., 1991, 30(B), 46.403. J. Zamocka, D. Dvoracknov, J. Heger, A. Nagy and D. Mynorcik ; Chem. Zveshi1980, (34), 556 ; Chem. Abstr., 1981, 94, 139741b.404. Wellinga Kobus, Eussen Jacobus H. H. ; Eur. Pat. EP 1988, 269 141 (Cl C07D231/06) ; Chem. Abstr., 1989, 110, 8204.405. Uhlendorf Joachim Kubl. Peter, Leyck, Sigurd ; Ger. Off. DE 1988, 3, 705, 933 (ClC07D 417104) ; Chem. Abstr., 1989, 110, 389870.406. K. Tern and Zolzislaw ; Acta. Pol. Pharm., 1979, 36(3), 227 ; Chem. Abstr., 1980,93, 4650r.407. V. S. Jolly and Manish Pathak ; J. Ind. Chem. Soc., 1991, 68, 304.408. M. Koos, M. Repas, B. Steiner, D. Myanrnick ; Chem. Pap. 1990, 44(1), 105-10 ;Chem. Abstr., 1990, 113, 78232y.409. Yamashita Hiroyuti, Odata Mocoto, Lizuka et al. ; Eur. Pat. Appl. EP 295695 (ClC07D 401/6) ; Chem. Abstr., 1989, 111, 23510.410. G. R. Subbanwad and Y. B. Vibhuta ; J. Indian Chem. Soc. 1992, 69, 781.411. F. M. Abd-El-Latif, M. A. Barsi, As. Maghraby, M. Z. Abady and D. Dopi ; J. IndianChem. Soc. 1995, 72, 641-643.412. Ismail, Mohamed Mohsen, El-Gendy, Adel A., Abdou, Madia A., El-Falaha, BhagatM. A.., Alexandria ; J. Pharm. Sci. 1993, 7(1), 41-4 ; Chem. Abstr., 1996, 124,8687d.182References…..
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Page 3:
The Sarvodaya Education Society’s
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selfless help, moral support and gu
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Introduction and Spectral studies .
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“STUDIES ON SOME HETEROCYCLICENTI
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Pyrimidine derivatives have been pr
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Isoxazole derivative synthesized by
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“STUDIES ON SOMEHETEROCYCLIC ENTI
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(b) Pharmacokinetics: It is derived
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(C) Drug DevelopmentMany natural pr
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The process of drug design is exten
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(l) Non steroidal anti-inflammatory
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INTRODUCTIONThe aza-indolizine cont
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PHARMACEUTICAL IMPORTANTMuch resear
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Compd. R 1 R 2 R 3a :- H 7-Me-6,8-B
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S. Kristjan, Gudmundsson and A. Bra
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STUDIES ON IMIDAZOPYRIDINE DERIVATI
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(a) Chalcones with monoethanolamine
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Das B.P. et al. 111 have found that
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Furthermore, Alcaraz M.J, et al. 13
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REACTION SCHEMECl+ClOClOClClCH 3NH
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Instrument : SHIMADZU FTIR 8400 Spe
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SignalNo.SignalPosition(δppm)Relat
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ANTIMICROBIAL ACTIVITYProducts : Ch
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The reaction mixture was poured on
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TABLE NO.- 1A BIOLOGICAL SCREENING
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PART-IISTUDIES ON PYRIMIDINES
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The self consistent (pi)electron de
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class of dye viz. trichloro pyrimid
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ability to cleave nucleic acid targ
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SSNHNHoONOoONOo(11) (12)oOHThe Pyri
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called ABPP or bropirimine(2-amino-
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acid so that it could be utilized f
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have reported the 5-substitutedfuro
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maturation of the viral mRNA molecu
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Nevertheless, these compounds const
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OHHNCH 3Cl(CH 2 )nSNNR 2R 1N H 2NSR
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SECTION-ISTUDIES ONOXOPYRIMIDINES
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PHARMACEUTICAL IMPORTANCEIn recent
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REACTION SCHEMECH 3NNCHOCl10% KOH R
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INSTRUMENT :SHIMADZU FTIR 8400 Spec
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EXPERIMENTALSynthesis and therapeut
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TABLE NO.- 2(IB)PHYSICAL CONSTANTS
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INTRODUCTIONThiopyrimidine derivati
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H 3 COHNRH 3 CH 3 CNHS( IV ) R = ar
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SYNTHESIS AND THERAPEUTIC EVALUATIO
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IR SPECTRAL STUDIES OF 6-(2-(4-CHLO
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NMR SPECTRAL STUDIES OF 6-(2-(4-CHL
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MASS SPECTRAL STUDIES OF 6-(2-(4-CH
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[F] Antimicrobial activity of 6-(2-
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SECTION-IIISTUDIES ONAMINOPYRIMIDIN
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ArCHO+ArCOCH3NaOHMethanolR R 1ONaOH
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IR SPECTRAL STUDIES OF 4-(2-(4-CHLO
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NMR SPECTRAL STUDIES OF 4-(2-(4-CHL
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MASS SPECTRAL STUDIES OF 4-(2-(4-CH
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[F] Antimicrobial activity of 4-(2-
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PART-IIISTUDIES ONCYCLOHEXENONES
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2. Michael addition of chalcone wit
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Rheinheimer J. et al. 381have synth
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IR SPECTRAL STUDIES OF ETHYL-6-(2-(
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NMR SPECTRAL STUDIES OF ETHYL-6-(2-
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MASS SPECTRAL STUDIES OF ETHYL-6-(2
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Antimicrobial testing was carried o
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PART-IVSTUDIES ON PYRAZOLINES
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H 2 C= CHCN + Ar - NHNH 2NArN(3) 2
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PHARMACEUTICAL IMPORTANCE :2- Pyraz
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Kadu et al. 424 and antimicrobial b
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REACTION SCHEMECH 3NNClCHO10% KOHRO
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Instrument : SHIMADZU FTIR 8400 Spe
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EXPERIMENTALSynthesis and therapeut
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TABLE NO.- 4(B)PHYSICAL CONSTANTS O
Page 153 and 154: INTRODUCTION:Isoxazole come under t
Page 155 and 156: PHARMACEUTICAL IMPORTANCE :Isoxazol
Page 157 and 158: SYNTHESISAND THERAPEUTIC EVALUATION
Page 159 and 160: IR SPECTRAL STUDIES OF 2-(4-CHLOROP
Page 161 and 162: NMR SPECTRAL STUDIES OF 2-(4-CHLORO
Page 163 and 164: MASS SPECTRAL STUDIES OF 2-(4-CHLOR
Page 165 and 166: [F]Antimicrobial activity of 2-(4-c
Page 167 and 168: PART-VISTUDIES ON OXIRANES
Page 169 and 170: ( iii ) Epoxidation can also been c
Page 171 and 172: Moreover, Nomura Yutaka et al. 487
Page 173 and 174: SYNTHESIS AND THERAPEUTIC EVALUATIO
Page 175 and 176: IR SPECTRAL STUDIES OF (3-(2-(4-CHL
Page 177 and 178: NMR SPECTRAL STUDIES OF (3-(2-(4-CH
Page 179 and 180: MASS SPECTRAL STUDIES OF (3-(2-(4-C
Page 181 and 182: [F] Antimicrobial activity of (3-(2
Page 184 and 185: 1. J. A. Joule and K. Mills; Hetero
Page 186 and 187: 37. James J. Kaminski, D. G. perkin
Page 188 and 189: 78. Ms. B. S. Hastak and B. J. Ghiy
Page 190 and 191: 116. V. R. Mudalir and V. Joshi ; I
Page 192 and 193: 150. S. Inoue, A. J. Saggimoto and
Page 194 and 195: 197. S. S. Bahekar, D. B. Shinde; A
Page 196 and 197: 238. A. Kreutzberger and M. Sellhei
Page 198 and 199: 280. See, for example, W. H. Prusof
Page 200 and 201: 326. C. W. Whitehead and J. J. Trav
Page 202 and 203: 366. Nagarjan K., Shenoy S. J.; Ind
Page 206 and 207: 432. Solankee Sejal; Prajapati Yoge
Page 208 and 209: 463. Mishra Ashutosh ; Jain Sanmati
Page 210 and 211: 496. Kaneko Mashami, Saitoh Yutaka,
Page 212 and 213: CH 3CH 3NNClNNClORHNONRRRC 6 H 5 -
Page 214 and 215: CH 3CH 3NNClNNClEtOOCORHNNRRRC 6 H
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