Essentials of Organic Chemistry

ISBN-13: 9780470016664 / Angielski / Miękka / 2006 / 720 str.

P M Dewick

Opis

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.

Recenzje

"The ease with which the author conveys predictability in fundamental chemical reaction pathways distinguishes this book." ( Journal of Medicinal Chemistry, 2007)

"...the textbook accomplishes its distinctive purpose with clear writing and appropriately selected content" (Journal of Natural Products, 2007)

"Do you want to add life to your organic chemistry course? If so, Essentials of Organic Chemistry (1) may be for you." (Journal of Chemical Education, February 2008)

"...the book is a very good experience of an organic chemistry mechanistic approach to the study of biochemistry " (Physical Sciences Educational Reviews, December 2006)

Spis treści

Preface.

1. Molecular representations and nomenclature.

2. Atomic structure and bonding.

3. Stereochemistry.

4. Acids and bases.

5. Reaction mechanisms.

6. Nucleophilic reactions: nucleophilic substitution.

7. Nucleophilic reactions of carbonyl groups.

8. Electrophilic reactions.

9. Radical reactions.

10. Nucleophilic reactions involving enolate anions.

11. Heterocycles.

12. Carbohydrates.

13. Amino acids, peptides and proteins.

14. Nucleosides, nucleotides and nucleic acids.

15. The organic chemistry of intermediary metabolism.

16. How to approach examination questions: selected problems and answers.

Index.

O autorze

Dr Paul Dewick, School of Pharmacy, University of Nottingham, Nottigham NG7 2RD
Paul Dewick is the author of the successful Medicinal Natural Product, 2/E and is a well–respected academic within his field.