Heterocyclic chemistry is an expanding subject, thanks to the research currently being done in the field. Heterocyclic components have many diverse applications in pharmacy, medicine, agriculture and other life sciences, so there is a constant need for updated information. This fourth edition retains many of the features that have proved successful in prior editions. It consists of 11 comprehensive chapters which discuss the heterocyclic components ring by ring with an emphasis on the stereochemistry of reactions and their mechanisms. Each chapter is very well referenced, with a thoroughly updated bibliography and contains a set of self assessment problems at the end for the reader to answer. The book is intended for use as a textbook on courses in heterocyclic chemistry, but it is also relevant to biochemistry, pharmacy and medicine, and will be a valuable addition to any medical or life science library.
Three Membered Heterocyclic Compounds
Four Membered Heterocyclic Compounds
Five Membered Heterocyclic Compounds
7 other sections not shown
3-position acetic acid adduct aldehydes alkaloids alkene alkyl amine Angew anhydride aromatic azetidine aziridine azirine basic benzene benzene ring benzo benzofuran benzothiophene bond Bromination carbon atoms carbonyl Chem Chemical Reactions chloride Comm condensation COOC2H5 COOCH COOH cyclization cycloaddition derivatives diaziridine dipole electron electrophilic attack electrophilic substitution epoxide equation ester formation furan give halogen hetero atom Heterocyclic Chem Heterocyclic Chemistry Heterocyclic Compounds heterocyclic ring hydrogen ibid imidazole indole intermediate involves irradiation isomeric isoquinoline isothiazole isoxazole ketone letters methyl mixture molecule N-oxide nitration nitrogen atom nucleophilic obtained occurs oxaziridine oxazole oxetane oxidizing agents oxirane oxygen prepared presence proton pyrazole pyridazine pyridine pyrimidine pyrrole pyrylium quinoline reactive reacts rearrangement refluxing resonance ring closure ring opening ring system salts sodium solvents stable structure sulfonation sulfur synthesis Synthetic Methods takes place tautomeric temperature Tetrahedron thiazole thietane thiirane thiophene undergo y-pyrones yields