Essentials of Organic Chemistry: For Students of Pharmacy, Medicinal Chemistry and Biological Chemistry
John Wiley & Sons, Mar 20, 2013 - 704 pages
Essentials of Organic Chemistry is an accessible introduction to the subject for students of Pharmacy, Medicinal Chemistry and Biological Chemistry. Designed to provide a thorough grounding in fundamental chemical principles, the book focuses on key elements of organic chemistry and carefully chosen material is illustrated with the extensive use of pharmaceutical and biochemical examples.
In order to establish links and similarities the book places prominence on principles and deductive reasoning with cross-referencing. This informal text also places the main emphasis on understanding and predicting reactivity rather than synthetic methodology as well as utilising a mechanism based layout and featuring annotated schemes to reduce the need for textual explanations.
* tailored specifically to the needs of students of Pharmacy Medical 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 Pharmacy Medicinal and Biological Chemistry.
What people are saying - Write a review
We haven't found any reviews in the usual places.
Acids and bases
Nucleophilic reactions of carbonyl groups
Nucleophilic reactions involving enolate anions
Other editions - View all
Essentials of Organic Chemistry: For Students of Pharmacy, Medicinal ...
Paul M. Dewick
Limited preview - 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