Organic Chemistry Concepts and Applications for Medicinal Chemistry
Autor Joseph E. Riceen Limba Engleză Paperback – 25 iun 2014
- Focused approach to review those organic chemistry concepts that are most important for medicinal chemistry practice and understanding
- Accessible content to refresh the reader's knowledge of bonding, structure, functional groups, stereochemistry, and more
- Appropriate level of coverage for students in organic chemistry, medicinal chemistry, and related areas; individuals seeking content review for graduate and medical courses and exams; pharmaceutical patent attorneys; and chemists and scientists requiring a review of pertinent material
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Specificații
ISBN-13: 9780128007396
ISBN-10: 0128007397
Pagini: 224
Ilustrații: 130 illustrations
Dimensiuni: 152 x 229 x 12 mm
Greutate: 0.3 kg
Editura: ELSEVIER SCIENCE
ISBN-10: 0128007397
Pagini: 224
Ilustrații: 130 illustrations
Dimensiuni: 152 x 229 x 12 mm
Greutate: 0.3 kg
Editura: ELSEVIER SCIENCE
Public țintă
Advanced students moving from organic chemistry to medicinal/pharmaceutical chemistry; exam takers in pharmacy, medicine, etc; professionals in chemistry and pharmaceutics who require review for practiceCuprins
1. Bonding in Organic Compounds a. Atomic Orbitals b. Hybrid Orbitals c. Resonance d. Aromaticity2. The Three-Dimensional Structure of Organic Compounds a. Isomers b. Stereoisomerism at Saturated Centers c. Prochirality d. Conformations3. Functional Groups a. Common Functional Groups b. The Electronic Effects of Functional Groups4. Acids and Bases a. Bronsted-Lowry Acids and Bases b. Ionization c. Estimating Acid/Base Strength d. Lewis Acids and Bases5. Partition Coefficients a. What is a Partition Coefficient? b. Effect of Structure on Partition Coefficients6. The Nomenclature of Cyclic and Polycyclic Compounds a. Common Heterocycles b. Fused-Ring Systems c. Substituents and Saturation d. Bridged-Rings e. Spiro-Rings f. Special Classes of Compounds i. Steroids ii. Prostaglandins iii. Morphinans7. Drug Metabolism a. Phase I – Oxidative Processes b. Phase I – Reductions c. Phase I – Hydrolysis d. Phase II – Conjugation e. Miscellaneous Phase II Processes