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Instrument : SHIMADZU FTIR 8400 Spectrophotometer; Frequency range:4000-400 cm -1 (KBr disc.)Frequency in cm -1Type Vibration ModeObserved ReportedRef.Alkane C-H str.(asym.) 2925 2975-2950 143-a-CH 3 C-H str.(sym.) 2880 2880-2860 ”C-H i.p.def 1450 1470-1435 ”C-H o.o.p.def. 1386 1395-1370 ”Aromatic C-H str. 3066 3090-3030 143-bC=C Str. 1504 1520-1480 ”C-H i.p.def 1116 1125-1090 ”C-H o.o.p.def. 835 835-810 ”Moiety C=N str. 1620 1610-1590 143-cC-N str. 1190 1230-1020 ”C-Cl str. 756 800-750 ”C=O str. 1620 1700-1640 ”Ether(Epoxide)C-O-C str. 825 865-785 143-d155Oxirane…..
NMR SPECTRAL STUDIES OF (3-(2-(4-CHLOROPHENYL)-8-METHYL-1H-IMIDAZO[1,2-a]PYRIDINE-3-YL)OXIRANE-2-YL)(4-METHOXYPHENYL)METHAN-ONE.Internal Standard : TMS; Solvent : DMSO; Instrument : BRUKER Spectrometer(400MHz)156Oxirane…..
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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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SignalNo.SignalPosition(δppm)Relat
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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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SYNTHESIS AND THERAPEUTIC EVALUATIO
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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
Page 125 and 126: SYNTHESIS AND THERAPEUTIC EVALUATIO
Page 127 and 128: IR SPECTRAL STUDIES OF ETHYL-6-(2-(
Page 129 and 130: NMR SPECTRAL STUDIES OF ETHYL-6-(2-
Page 131 and 132: MASS SPECTRAL STUDIES OF ETHYL-6-(2
Page 133 and 134: Antimicrobial testing was carried o
Page 135 and 136: PART-IVSTUDIES ON PYRAZOLINES
Page 137 and 138: H 2 C= CHCN + Ar - NHNH 2NArN(3) 2
Page 139 and 140: PHARMACEUTICAL IMPORTANCE :2- Pyraz
Page 141 and 142: Kadu et al. 424 and antimicrobial b
Page 143 and 144: REACTION SCHEMECH 3NNClCHO10% KOHRO
Page 145 and 146: Instrument : SHIMADZU FTIR 8400 Spe
Page 147 and 148: SignalNo.SignalPosition(δppm)Relat
Page 149 and 150: EXPERIMENTALSynthesis and therapeut
Page 151 and 152: 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: IR SPECTRAL STUDIES OF (3-(2-(4-CHL
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 204 and 205: 396. Ausra Voskiene,Vytautas Mickev
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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