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|a 9780857111593
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|z 9780857110831
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|a 615.1/9
|2 23
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|a UAMI
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| 100 |
1 |
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|a Barlow, D.
|q (David),
|d 1954-
|e author.
|1 https://id.oclc.org/worldcat/entity/E39PCjwQhXXmXP6HTJDJhPTdV3
|
| 245 |
1 |
0 |
|a Chemistry of drugs /
|c David Barlow, David Mountford.
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| 264 |
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1 |
|a London :
|b Pharmaceutical Press,
|c 2014.
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| 300 |
|
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|a 1 online resource (x, 260 pages) :
|b illustrations
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| 336 |
|
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|a text
|b txt
|2 rdacontent
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| 337 |
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|a computer
|b c
|2 rdamedia
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| 338 |
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|a online resource
|b cr
|2 rdacarrier
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| 490 |
1 |
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|a FASTtrack
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| 588 |
0 |
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|a Print version record.
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| 505 |
0 |
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|6 880-01
|a Cover; Title Page; Copyright; Contents; Introduction to the FASTtrack series; Preface; About the authors; Chapter 1. Chemical structure and bonding; Cations and anions; Electron orbitals; Electronic configuration; Molecular orbitals; Promotion; Hybridisation; Bonding; Valence shell electron pair repulsion (VSEPR); Nucleophiles and electrophiles; Drawing chemical structures; Resonance/mesomerism; Drawing resonance hybrids; Self-assessment; Chapter 2. Intermolecular interactions; Importance of intermolecular interactions in pharmacy; Coulombic/electrostatic interactions.
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| 505 |
8 |
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|a Van der Waals interactionsHydrogen bond interactions; Molecular affinity and the free energy of interaction; Self-assessment; Chapter 3. Acids and bases; Definitions of acids and bases; Acid and base strength; Quantifying the strengths of acids and bases: pKa and pKb values; Importance of acids and bases in pharmacy; Common acidic and basic functional groups; pH and pKa; Amphoteric compounds; Simple buffer solutions; Universal buffer solutions; Self-assessment; Chapter 4. Stereochemistry; Stereochemistry and its importance in pharmaceutical science; Stereoisomers.
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| 505 |
8 |
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|a Fischer's convention of stereochemical nomenclatureConformational isomers; Stereoisomers of cyclic molecules; Geometric isomers; Topological isomers; Self-assessment; Chapter 5. Chemical reaction mechanisms; Nucleophiles and electrophiles; Reaction mechanisms; Curly arrows in reaction mechanisms; Radicals in reaction mechanisms; Fish hooks in reaction mechanisms; Chemical reactivity; Self-assessment; Chapter 6. Chemistry of electrophiles and nucleophiles; Addition and substitution reactions; Electrophilic addition; Nucleophilic substitution; Elimination reactions.
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| 505 |
8 |
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|a Competition between substitution and eliminationSelf-assessment; Chapter 7. Chemistry of aromatic compounds; Benzene; Naming of benzene derivatives; Reactivity; Electrophilic substitution; Electrophilic substitution versus electrophilic addition; Examples of electrophilic substitution; Monosubstituted benzene derivatives; Halogen substituents; Disubstituted benzene derivatives; Self-assessment; Chapter 8. Chemistry of carbonyl compounds; Reactivity of the carbonyl group; Nucleophilic addition; Changes in hybridisation during nucleophilic addition; Stereochemistry in nucleophilic addition.
|
| 590 |
|
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|a ProQuest Ebook Central
|b Ebook Central Academic Complete
|
| 650 |
|
0 |
|a Pharmaceutical chemistry
|x Examinations
|v Study guides.
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| 650 |
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0 |
|a Drugs
|x Design
|x Examinations
|v Study guides.
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| 650 |
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0 |
|a Pharmacy
|x Examinations
|v Study guides.
|
| 650 |
|
0 |
|a Drugs
|x Design.
|
| 650 |
1 |
2 |
|a Chemistry, Pharmaceutical
|x education
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| 650 |
2 |
2 |
|a Drug Design
|
| 650 |
2 |
2 |
|a Education, Pharmacy
|
| 650 |
|
6 |
|a Chimie pharmaceutique
|x Examens
|v Guides de l'étudiant.
|
| 650 |
|
6 |
|a Médicaments
|x Conception
|x Examens
|v Guides de l'étudiant.
|
| 650 |
|
6 |
|a Médicaments
|x Conception.
|
| 650 |
|
7 |
|a MEDICAL
|x Pharmacology.
|2 bisacsh
|
| 650 |
|
7 |
|a Drugs
|x Design
|2 fast
|
| 650 |
|
7 |
|a Pharmacy
|x Examinations
|2 fast
|
| 655 |
|
2 |
|a Problems and Exercises
|
| 655 |
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2 |
|a Study Guide
|
| 655 |
|
7 |
|a exercise books.
|2 aat
|
| 655 |
|
7 |
|a Problems and exercises
|2 fast
|
| 655 |
|
7 |
|a Study guides
|2 fast
|
| 655 |
|
7 |
|a Problems and exercises.
|2 lcgft
|
| 655 |
|
7 |
|a Problèmes et exercices.
|2 rvmgf
|
| 700 |
1 |
|
|a Mountford, David,
|e author.
|
| 758 |
|
|
|i has work:
|a Chemistry of drugs (Text)
|1 https://id.oclc.org/worldcat/entity/E39PCFJ7DdmDVdJ8VKcTc9vxH3
|4 https://id.oclc.org/worldcat/ontology/hasWork
|
| 776 |
0 |
8 |
|i Print version:
|a Barlow, D. (David), 1954-
|t Chemistry of drugs
|z 9780857110831
|w (OCoLC)884551455
|
| 830 |
|
0 |
|a FASTtrack.
|
| 856 |
4 |
0 |
|u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=1790794
|z Texto completo
|
| 880 |
8 |
|
|6 505-01/(S
|a Examples of nucleophilic additionAddition of amines -- imine and enamine formation; Reductive amination; Addition-elimination; Changes in hybridisation during addition-elimination; Examples of addition-elimination; α-Hydrogen reactivity; Examples of α-hydrogen reactions; Conjugate addition (Michael addition); Examples of conjugate addition; Reaction with amines and thiols; Self-assessment; Chapter 9. Chemistry of aromatic heterocyclic compounds; Aromaticity in heterocyclic compounds; Naming of heteroaromatic compounds; The basicity of nitrogen heterocyclic compounds.
|
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|a Askews and Holts Library Services
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|a EBL - Ebook Library
|b EBLB
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| 938 |
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|a EBSCOhost
|b EBSC
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|a ProQuest MyiLibrary Digital eBook Collection
|b IDEB
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