A Textbook Of Pharmaceutical Organic Chemistry - III

1. Stereo Isomerism : Optical Isomerism
1.1 Optical activity, enantiomerism, diastereoisomers, meso compounds
1.2 Elements of symmetry, chiral and achiral molecules
1.3 DL system of nomenclature of optical isomers, sequence rules, RS system of nomenclature of optical isomers
1.4 Reactions of chiral molecules
1.5 Racemic modification and resolution of racemic mixture.
1.6 Asymmetric synthesis: partial and absolute

2. Stereo Isomerism : Geometrical Isomerism
2.1 Nomenclature of geometrical isomers (Cis Trans, EZ, Syn, Anti systems),
2.2 Methods of determination of configuration of geometrical isomers.
2.3 Conformational isomerism in Ethane, n-Butane and Cyclohexane.
2.4 Stereo isomerism in biphenyl compounds (Atropisomerism) and conditions for optical activity.
2.5 Stereospecific and stereoselective reactions.

3. Heterocyclic Compounds : I
3.1 Nomenclature and classification, synthesis, reactions and medicinal uses of following compounds/derivatives: Pyrrole, Furan, and Thiophene
3.2 Relative aromaticity and reactivity of Pyrrole, Furan and Thiophene.

4. Heterocyclic Compounds : II
4.1 Synthesis, reactions and medicinal uses of following compounds/derivatives: Pyrazole, Imidazole, Oxazole and Thiazole, Pyridine, Quinoline, Isoquinoline, Acridine and Indole.
4.2 Basicity of Pyridine.
4.3 Synthesis and medicinal uses of Pyrimidine, Purine, Azepines and their derivatives.

5. Reactions of Synthetic Importance
5.1 Metal hydride reduction (NaBH4 and LiAlH4)
5.2 Diisobutylaluminium hydride
5.3 Lithium Aluminium Hydride
5.4 Sodium Borohydride
5.5 Sodium Cyanoborohydride
5.6 Sodium Hydride
5.7 Birch Reduction
5.8 Clemmensen Reduction
5.9 Beckmann Rearrangement
5.10 Claisen-Schmidt Condensation
5.11 Oppenauer Oxidation
5.12 Wolf-Kishner Reduction
5.13 Dakin Oxidation
5.14 Schmidt Reaction