Heterocyclic Chemistry

Paper Code: 
CHY 423 (B)
Credits: 
4
Contact Hours: 
60.00
Max. Marks: 
100.00
Objective: 

Course Objectives :

The course aims to provide a broad introduction to heterocyclic chemistry and its nomenclature. Emphasis is given on some important heterocyclic systems, such as aziridines, oxiranes, oxetanes, benzopyrroles, benzofurans, benzothiophenes, pyrones, diazines, triazines, thiazines, and meso-ionic heterocycles. For each group, students will be acquainted with ring synthesis, chemical properties and characteristic reactions.

Course Outcomes (Cos):                                                                                                                                   

COURSE

Learning outcomes (at course level)

Learning and teaching strategies

Assessment Strategies

Paper Code

Paper Title

CHY 423(B)

Heterocyclic Chemistry

The students will be able to-

 

CO142-learn and understand the specific properties and biological activities of some important heterocycles.

CO143-describe mechanisms for reactions involving heterocycles as starting materials, intermediates and products, and be able to propose syntheses of heterocycles from the major classes and assign their names.

 Interactive Lectures

 

Discussions

 

Tutorials

 

Quiz

 

Problem solving

PowerPoint Presentation

 

Written test

 

Google Quiz

 

Assignment

 

Semester End Exam

 

 

12.00
Unit I: 
Introduction and Nomenclature of Heterocycles

Replacement and systematic nomenclature (Hantzsch-Widman system) for monocyclic, fused and bridged heterocycles.

General chemical behaviour of aromatic heterocycles, classification (structural type), criteria of aromaticity (bond lengths, ring current and chemical shifts in 1H NMR-spectra, empirical resonance energy, delocalization energy and Dewar resonance energy, diamagnetic susceptibility exaltations), heteroaromatic reactivity and tautomerism in aromatic heterocycles.

12.00
Unit II: 
Conformational Analysis of Non-aromatic Heterocycles

Strain-bond angle, torsional strains and their consequences in small ring heterocycles. Conformation of six-membered heterocycles with reference to molecular geometry, barrier to ring inversion, pyramidal inversion and 1,3-diaxial interaction, stereo-electronic effects:  Anomeric and related effects, attractive interactions:  Hydrogen bonding and intermolecular nucleophilic-electrophilic interactions.

12.00
Unit III: 
Small Ring Heterocycles

Three-membered and four membered heterocycles: Synthesis and reactions of aziridines, oxiranes, thiiranes, azetidines, oxetanes and thietanes, five membered heterocycles: synthesis and reactions of different isomers of diazoles (pyrazoles, imidazoles), oxazoles, thiazoles, 1,2,4-triazole, oxadiazole, thiadiazole, 1,2,3,4-tetrazole.Porphyrins and applications.

12.00
Unit IV: 
Benzo-Fused Five-Membered Heterocycles and MesoIonic

Synthesis and reactions including medicinal applications of benzopyrroles, benzofurans and benzothiophenes. Meso-ionic heterocycles: Classification, chemistry of some important meso-ionic heterocycles of type-A and B and their applications. Sydnones.

12.00
Unit V: 
Six Membered Heterocycles

With one heteroatom: Synthesis and reactions of pyrilium salts and pyrones and their comparison with pyridinium and thiopyrylium salts and pyridones; synthesis and reactions of quinolizinium and benzopyrylium salts, coumarins and chromones.

With two or more heteroatoms: Synthesis and reactions of diazines, triazines, tetrazines and thiazines.Some important macroheterocycles.

References: 
  • Heterocyclic Chemistry Vol. I & II; First Edition; R.R. Gupta and M. Kumar; Springer (India) Pvt. Ltd., 2011.
  • Heterocyclic Chemistry; Fifth Edition; J.A. Joule and K.Mills;Wiley-Blackwell, London, 2013.
  • Heterocyclic Chemistry; Third Edition; T.L. Gilchrist; Pearson Education,Delhi,2005.
  • An Introduction to the Chemistry of Heterocyclic Compounds; Third Edition; R.M. Acheson; Wiley Eastern Ltd, New Delhi,1976.
  • Contemporary Heterocyclic Chemistry; First Edition, G.R. Newkome and W.W. Paudler, Wiley Interscience, 1982.

 

Academic Year: