Essentials of Organic Chemistry: For Students of Pharmacy, Medicinal Chemistry and Biological Chemistry
John Wiley & Sons, 20 մրտ, 2013 թ. - 704 էջ
Essentials of Organic Chemistry is an accessible introduction tothe subject for students of Pharmacy, Medicinal Chemistry andBiological Chemistry. Designed to provide a thorough grounding infundamental chemical principles, the book focuses on key elementsof organic chemistry and carefully chosen material is illustratedwith the extensive use of pharmaceutical and biochemicalexamples.
In order to establish links and similarities the book placesprominence on principles and deductive reasoning withcross-referencing. This informal text also places the main emphasison understanding and predicting reactivity rather than syntheticmethodology as well as utilising a mechanism based layout andfeaturing annotated schemes to reduce the need for textualexplanations.
* tailored specifically to the needs of students of PharmacyMedical Chemistry and Biological Chemistry
* numerous pharmaceutical and biochemical examples
* mechanism based layout
* focus on principles and deductive reasoning
This will be an invaluable reference for students of PharmacyMedicinal and Biological Chemistry.
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Acids and bases
Nucleophilic reactions of carbonyl groups
Nucleophilic reactions involving enolate anions
Այլ խմբագրություններ - View all
Essentials of Organic Chemistry: For Students of Pharmacy, Medicinal ...
Paul M. Dewick
Դիտել հնարավոր չէ - 2006
acetic acetyl-CoA acyl addition alcohol aldehyde aldol reaction alkene alkyl allylic amide amine amino acid anhydride atom basic benzene carbon carbonyl carbonyl group carboxylic acid cation CH2OH CH3 H chain chiral centre chloride Claisen reaction CO2Et CO2H compounds conﬁguration conformer conjugate acid conjugate base cyclic delocalization derivatives diphosphate double bond electrons electrophilic enantiomer energy enolate anion enzyme equilibrium ester favourable ﬁrst formation H CH3 H H H H H OH hemiacetal heterocycle HO2C hydride hydrolysis hydroxyl imine inductive effect intermediate involves ionization isomer ketone leaving group lone pair mechanism methyl molecule nitrogen nucleophilic attack OH H OH OH orbitals oxidation oxygen peptide phenol phosphate pKa values planar priority protein proton pyridine pyrrole racemic radical react reactive reagent residues resonance stabilization ring system SCoA Section sequence side-chains SN2 reaction speciﬁc substituents substrate synthesis tautomerism