- Page 2 and 3: Chemistry for Pharmacy Students Gen
- Page 4: This book is dedicated to pharmacy
- Page 7 and 8: viii CONTENTS 5.5 Substitution reac
- Page 9 and 10: x PREFACE countries. Therefore, the
- Page 12 and 13: 1 Introduction Learning objectives
- Page 14 and 15: Whatever the source is, chemistry i
- Page 16 and 17: 1.2 PHYSICAL PROPERTIES OF DRUG MOL
- Page 18 and 19: Each acid has a conjugate base, and
- Page 20 and 21: 1.2 PHYSICAL PROPERTIES OF DRUG MOL
- Page 22 and 23: CH3CH3 ðEthaneÞ !CH3NH2 ðMethyla
- Page 26: Recommended further reading RECOMME
- Page 29 and 30: 18 CH2 ATOMIC STRUCTURE AND BONDING
- Page 31 and 32: 20 CH2 ATOMIC STRUCTURE AND BONDING
- Page 33 and 34: 22 CH2 ATOMIC STRUCTURE AND BONDING
- Page 35 and 36: 24 CH2 ATOMIC STRUCTURE AND BONDING
- Page 37 and 38: 26 CH2 ATOMIC STRUCTURE AND BONDING
- Page 39 and 40: 28 CH2 ATOMIC STRUCTURE AND BONDING
- Page 41 and 42: 30 CH2 ATOMIC STRUCTURE AND BONDING
- Page 43 and 44: 32 CH2 ATOMIC STRUCTURE AND BONDING
- Page 46 and 47: 3 Stereochemistry Learning objectiv
- Page 48 and 49: dimensional orientation of the hydr
- Page 50 and 51: H H H H H H H H H H H C 3 Butane Am
- Page 52 and 53: Again, in reality, cyclohexane is n
- Page 54 and 55: not chiral. With achiral molecules,
- Page 56 and 57: 3.2 ISOMERISM 45 When we have a pai
- Page 58 and 59: ( ). This D and L system is common
- Page 60 and 61: HO H 4 1 2COOH CH2OH 3 (R)-2,3-Dihy
- Page 62 and 63: Geometrical isomers H H H H Cl Cl C
- Page 64 and 65: 3.3 SIGNIFICANCE OF STEREOISOMERISM
- Page 66 and 67: H H * * (+)-Limonene (in orange) (
- Page 68 and 69: 3.7 CHIRAL COMPOUNDS THAT DO NOT HA
- Page 70 and 71: 4 Organic functional groups Learnin
- Page 72 and 73: ðContinuedÞ Name General structur
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4.3 ALKANES, CYCLOALKANES AND THEIR
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drawn as solid wedges, and those po
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4.3 ALKANES, CYCLOALKANES AND THEIR
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CH4 + 2 O2 CO2 + 2 H2O CH3CH2CH + 2
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Reactivity of alkyl halides RHC CH2
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Alkanes can be prepared from alkyl
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4.3 ALKANES, CYCLOALKANES AND THEIR
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H OH OH H i. BH3 .THF H2O, H2SO4 or
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Nomenclature of thiols The nomencla
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H2C CH2 CH3CH CH2 CH3CH2CH CH2 O O
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Nomenclature of amines Aliphatic am
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aldehydes and ketones, followed by
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O C2H5 C 4.3 ALKANES, CYCLOALKANES
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earlier, alcohols can be prepared f
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Aliphatic dicarboxylic acids are na
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aldehydes (see Section 5.7.11), ozo
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4.3.14 Acid chlorides The functiona
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Preparation of acid anhydrides Anhy
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Reactions of esters Esters are less
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espectively (see Section 5.5.5). Th
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eagent or organolithium produces ke
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unsaturated groups are called the v
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Alkenes are obtained from selective
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equires two hybrid orbitals to bond
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addition reactions, e.g. hydrogenat
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4.6 AROMATIC COMPOUNDS AND THEIR DE
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4.6 AROMATIC COMPOUNDS AND THEIR DE
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4.6 AROMATIC COMPOUNDS AND THEIR DE
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form two doughnut-shaped clouds of
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4.6 AROMATIC COMPOUNDS AND THEIR DE
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4.6 AROMATIC COMPOUNDS AND THEIR DE
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the overlap of a p orbital on the s
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electrons from the ring through the
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CH 2 Br Bromomethylbenzene 4.6.10 P
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4.6 AROMATIC COMPOUNDS AND THEIR DE
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A number of other reactions can als
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Physical properties of aniline 4.6
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From chlorobenzene Treatment of chl
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4.6 AROMATIC COMPOUNDS AND THEIR DE
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4.6 AROMATIC COMPOUNDS AND THEIR DE
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4.7 HETEROCYCLIC COMPOUNDS AND THEI
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4.7 HETEROCYCLIC COMPOUNDS AND THEI
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4.7.4 PYRROLE, FURAN AND THIOPHENE:
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Furan is synthesized by decarbonyla
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N H S + HNO 3 + HNO 3 Acetic anhydr
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dipole moment of pyridine is 1.57 D
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N Cl 2-Chloropyridine Br N OMe 4-Br
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R' R NH 2 O + R'' O X Base R' R O H
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for isoxazole, pyrazole and isothia
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A number of drug molecules contain
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4.7.9 Purine Purine contains a pyri
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4.7.10 Quinoline and isoquinoline 4
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MeO MeO MeO MeO NH 2 β-Phenylethyl
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at room temperature, and posseses a
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In the nucleotides, while the heter
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4.8.2 Structure of nucleic acids Pr
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Sugar _ phosphate backbone O O P O
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Transcription: synthesis of RNA 4.8
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sample is obtained from a crime sce
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AVK (one letter). The ends of a pep
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Carbon CO 2 + H 2 O 4.9 AMINO ACIDS
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4.10 IMPORTANCE OF FUNCTIONAL GROUP
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4.10 IMPORTANCE OF FUNCTIONAL GROUP
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Certain functional groups in drug m
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192 CH5 ORGANIC REACTIONS Reaction
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194 CH5 ORGANIC REACTIONS H C 3 H +
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196 CH5 ORGANIC REACTIONS brominati
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198 CH5 ORGANIC REACTIONS General r
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200 CH5 ORGANIC REACTIONS Electroph
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202 CH5 ORGANIC REACTIONS addition
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204 CH5 ORGANIC REACTIONS Br. + Br.
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206 CH5 ORGANIC REACTIONS CH3CH CH2
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208 CH5 ORGANIC REACTIONS Hydrobora
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210 CH5 ORGANIC REACTIONS p bond, a
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212 CH5 ORGANIC REACTIONS Mechanism
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214 CH5 ORGANIC REACTIONS Addition
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216 CH5 ORGANIC REACTIONS molecule
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218 CH5 ORGANIC REACTIONS O R C Y Y
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220 CH5 ORGANIC REACTIONS condition
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222 CH5 ORGANIC REACTIONS Aldol con
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224 CH5 ORGANIC REACTIONS remove th
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226 CH5 ORGANIC REACTIONS formation
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228 CH5 ORGANIC REACTIONS Mechanism
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230 CH5 ORGANIC REACTIONS Stereoche
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232 CH5 ORGANIC REACTIONS E1 versus
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234 CH5 ORGANIC REACTIONS solvent i
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236 CH5 ORGANIC REACTIONS configura
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238 CH5 ORGANIC REACTIONS the base,
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240 CH5 ORGANIC REACTIONS Mechanism
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242 CH5 ORGANIC REACTIONS The react
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244 CH5 ORGANIC REACTIONS Conversio
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246 CH5 ORGANIC REACTIONS Mechanism
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248 CH5 ORGANIC REACTIONS Mechanism
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250 CH5 ORGANIC REACTIONS Conversio
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252 CH5 ORGANIC REACTIONS Preparati
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254 CH5 ORGANIC REACTIONS Nucleophi
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256 CH5 ORGANIC REACTIONS In the ca
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258 CH5 ORGANIC REACTIONS Cl 2 , Fe
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260 CH5 ORGANIC REACTIONS Step 3. L
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262 CH5 ORGANIC REACTIONS : O: R C
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264 CH5 ORGANIC REACTIONS water. Th
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266 CH5 ORGANIC REACTIONS Preparati
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268 CH5 ORGANIC REACTIONS work-up.
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270 CH5 ORGANIC REACTIONS (C5H5NH +
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272 CH5 ORGANIC REACTIONS OH Cyclop
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274 CH5 ORGANIC REACTIONS hydride s
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276 CH5 ORGANIC REACTIONS 5.7.20 Re
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278 CH5 ORGANIC REACTIONS Preparati
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280 CH5 ORGANIC REACTIONS Cyclic co
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282 CH5 ORGANIC REACTIONS with a mi
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284 CH6 NATURAL PRODUCT CHEMISTRY 6
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286 CH6 NATURAL PRODUCT CHEMISTRY t
- Page 299 and 300:
288 CH6 NATURAL PRODUCT CHEMISTRY L
- Page 301 and 302:
290 CH6 NATURAL PRODUCT CHEMISTRY C
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292 CH6 NATURAL PRODUCT CHEMISTRY O
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294 CH6 NATURAL PRODUCT CHEMISTRY p
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296 CH6 NATURAL PRODUCT CHEMISTRY I
- Page 309 and 310:
298 CH6 NATURAL PRODUCT CHEMISTRY T
- Page 311 and 312:
300 CH6 NATURAL PRODUCT CHEMISTRY P
- Page 313 and 314:
302 CH6 NATURAL PRODUCT CHEMISTRY M
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304 CH6 NATURAL PRODUCT CHEMISTRY a
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306 CH6 NATURAL PRODUCT CHEMISTRY h
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308 CH6 NATURAL PRODUCT CHEMISTRY H
- Page 321 and 322:
310 CH6 NATURAL PRODUCT CHEMISTRY H
- Page 323 and 324:
312 CH6 NATURAL PRODUCT CHEMISTRY C
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314 CH6 NATURAL PRODUCT CHEMISTRY 6
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316 CH6 NATURAL PRODUCT CHEMISTRY g
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318 CH6 NATURAL PRODUCT CHEMISTRY M
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320 CH6 NATURAL PRODUCT CHEMISTRY a
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322 CH6 NATURAL PRODUCT CHEMISTRY T
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324 CH6 NATURAL PRODUCT CHEMISTRY k
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326 CH6 NATURAL PRODUCT CHEMISTRY S
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328 CH6 NATURAL PRODUCT CHEMISTRY B
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330 CH6 NATURAL PRODUCT CHEMISTRY h
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332 CH6 NATURAL PRODUCT CHEMISTRY (
- Page 345 and 346:
334 CH6 NATURAL PRODUCT CHEMISTRY G
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336 CH6 NATURAL PRODUCT CHEMISTRY (
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338 CH6 NATURAL PRODUCT CHEMISTRY (
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340 CH6 NATURAL PRODUCT CHEMISTRY (
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342 CH6 NATURAL PRODUCT CHEMISTRY (
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344 CH6 NATURAL PRODUCT CHEMISTRY S
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346 CH6 NATURAL PRODUCT CHEMISTRY P
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348 CH6 NATURAL PRODUCT CHEMISTRY M
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350 CH6 NATURAL PRODUCT CHEMISTRY B
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352 CH6 NATURAL PRODUCT CHEMISTRY i
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354 CH6 NATURAL PRODUCT CHEMISTRY I
- Page 367 and 368:
356 CH6 NATURAL PRODUCT CHEMISTRY H
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358 CH6 NATURAL PRODUCT CHEMISTRY C
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360 CH6 NATURAL PRODUCT CHEMISTRY s
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362 CH6 NATURAL PRODUCT CHEMISTRY N
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364 CH6 NATURAL PRODUCT CHEMISTRY c
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366 CH6 NATURAL PRODUCT CHEMISTRY a
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368 CH6 NATURAL PRODUCT CHEMISTRY F
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370 CH6 NATURAL PRODUCT CHEMISTRY R
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372 INDEX Amino sugar 304, 305, 317
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374 INDEX Closed shell configuratio
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376 INDEX Friedel-Crafts alkylation
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378 INDEX Lincomycin 318 Linum usit
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380 INDEX Polymerization 106, 110 P
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382 INDEX Sulphanilamide 140 Sulpha