- Page 3: The Sarvodaya Education Society’s
- Page 6 and 7: selfless help, moral support and gu
- Page 9 and 10: Introduction and Spectral studies .
- Page 11 and 12: “STUDIES ON SOME HETEROCYCLICENTI
- Page 13 and 14: Pyrimidine derivatives have been pr
- Page 15 and 16: Isoxazole derivative synthesized by
- Page 17 and 18: “STUDIES ON SOMEHETEROCYCLIC ENTI
- Page 19 and 20: (b) Pharmacokinetics: It is derived
- Page 21 and 22: (C) Drug DevelopmentMany natural pr
- Page 23: The process of drug design is exten
- Page 27 and 28: INTRODUCTIONThe aza-indolizine cont
- Page 29 and 30: PHARMACEUTICAL IMPORTANTMuch resear
- Page 31 and 32: Compd. R 1 R 2 R 3a :- H 7-Me-6,8-B
- Page 33 and 34: S. Kristjan, Gudmundsson and A. Bra
- Page 35 and 36: STUDIES ON IMIDAZOPYRIDINE DERIVATI
- Page 37 and 38: (a) Chalcones with monoethanolamine
- Page 39 and 40: Das B.P. et al. 111 have found that
- Page 41 and 42: Furthermore, Alcaraz M.J, et al. 13
- Page 43 and 44: REACTION SCHEMECl+ClOClOClClCH 3NH
- Page 45 and 46: Instrument : SHIMADZU FTIR 8400 Spe
- Page 47 and 48: SignalNo.SignalPosition(δppm)Relat
- Page 49 and 50: ANTIMICROBIAL ACTIVITYProducts : Ch
- Page 51 and 52: The reaction mixture was poured on
- Page 53 and 54: TABLE NO.- 1A BIOLOGICAL SCREENING
- Page 55 and 56: PART-IISTUDIES ON PYRIMIDINES
- Page 57 and 58: The self consistent (pi)electron de
- Page 59 and 60: class of dye viz. trichloro pyrimid
- Page 61 and 62: ability to cleave nucleic acid targ
- Page 63 and 64: SSNHNHoONOoONOo(11) (12)oOHThe Pyri
- Page 65 and 66: called ABPP or bropirimine(2-amino-
- Page 67 and 68: acid so that it could be utilized f
- Page 69 and 70: have reported the 5-substitutedfuro
- Page 71 and 72: maturation of the viral mRNA molecu
- Page 73 and 74: Nevertheless, these compounds const
- Page 75 and 76:
OHHNCH 3Cl(CH 2 )nSNNR 2R 1N H 2NSR
- Page 77 and 78:
SECTION-ISTUDIES ONOXOPYRIMIDINES
- Page 79 and 80:
PHARMACEUTICAL IMPORTANCEIn recent
- Page 81 and 82:
REACTION SCHEMECH 3NNCHOCl10% KOH R
- Page 83 and 84:
INSTRUMENT :SHIMADZU FTIR 8400 Spec
- Page 85 and 86:
SignalNo.SignalPosition(δppm)Relat
- Page 87 and 88:
EXPERIMENTALSynthesis and therapeut
- Page 89 and 90:
TABLE NO.- 2(IB)PHYSICAL CONSTANTS
- Page 91 and 92:
INTRODUCTIONThiopyrimidine derivati
- Page 93 and 94:
H 3 COHNRH 3 CH 3 CNHS( IV ) R = ar
- Page 95 and 96:
SYNTHESIS AND THERAPEUTIC EVALUATIO
- Page 97 and 98:
IR SPECTRAL STUDIES OF 6-(2-(4-CHLO
- Page 99 and 100:
NMR SPECTRAL STUDIES OF 6-(2-(4-CHL
- Page 101 and 102:
MASS SPECTRAL STUDIES OF 6-(2-(4-CH
- Page 103 and 104:
[F] Antimicrobial activity of 6-(2-
- Page 105 and 106:
SECTION-IIISTUDIES ONAMINOPYRIMIDIN
- Page 107 and 108:
ArCHO+ArCOCH3NaOHMethanolR R 1ONaOH
- Page 109 and 110:
SYNTHESIS AND THERAPEUTIC EVALUATIO
- Page 111 and 112:
IR SPECTRAL STUDIES OF 4-(2-(4-CHLO
- Page 113 and 114:
NMR SPECTRAL STUDIES OF 4-(2-(4-CHL
- Page 115 and 116:
MASS SPECTRAL STUDIES OF 4-(2-(4-CH
- Page 117 and 118:
[F] Antimicrobial activity of 4-(2-
- Page 119 and 120:
PART-IIISTUDIES ONCYCLOHEXENONES
- Page 121 and 122:
2. Michael addition of chalcone wit
- Page 123 and 124:
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 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 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