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Front Matter; Preface; Contents; I. Benzofurans; 1. Introduction and Nomenclature; 2. Benzofuran and Its Alkyl Derivatives; A. Preparation; a. Catalytic Dehydrocyclization; b. Cyclizution of Allylphenols; c. Cyclodehydration of Ary foxy ketones; d. Rearrangement of' O-Aryloximes; e. Dehydrogenation of Bz-AIkyldihydrobenzofurans; f. Reduction of 2-Acetonyl-o-benzoquinols; g. Hydrogenation of 2-Acetylbenzofuran; h. Reaction of Copper Acetylides with Aryl Halides; i. Decarboxylation of Benzofurancarboxylic Acids; j. Photochemical Formation of Benzofurans; k. Adsorptive Cyclization
l. Condensation of Methylene Bis (ethyl sulfone)with Salicylaldehydes3. Aryl benzofurans; A. Preparation; a. Cychdehydration of w-Arloxyacetophenones; b. Condensation of Benzoins with Phenols; c. 1,3-Dipolar Additions of Oxocarbenes; d. Copper-Catalyzed Decomposition of Diazoketones; e. Ethynation of P-Benzoquinone; f Oxidation of Flavylium and Pyrylium Salts; g. Algar-Flynn-Oyamada Oxidation of 2'-Hydroxychalcones; h. Acid-Catalyzed Cyclization of O-Aryloximes; i. Photolytic Cyclizalions.; j. Miscellaneous; 4. Halobenzofurans; A. Caloro Derivatives; B. Bromo Derivatives; C. Iodo Derivatives
D. Fluoro Derivatives5. Nitrobenzofurans; 6. Benzofuranols; 7. Aminobenzofurans; 8. Benzofuranquinones; 9. Miscellaneous Reactions and Properties; A. Catalytic Hydrogenation; B. Oxidation; C. Ozonolysis; D. Nitration; E. Halogenation; F. Benzofuranylmetallic Compounds; G. Friedel-Crafts Techniques; H. Hoesch and Gatterman Techniques; I. With Diazoalkanes; J. With Dihalocarbene; K. Cyclophotochemical Addition; L. Polymerization; M. Miscellaneous Reactions; References; II. Acylbenzofurans; 1. Formylbenzofurans; 2. Acylbenzofurans; 3. Miscellaneous reactions; A. Reduction; B. Oxidation
C. Alkaline DegradationD. Rearrangement of Acylbenzofuran Oximes; E. Rearrangement (Migration) in Acylbenzofurans; F. Willgerodt-Kindler Reaction; G. Wittig Reaction; H. Miscellaneous; References; III. Benzofurancarboxylic acids; 1. Benzofuran monocarboxylic Acids; A. 2-Benzofurancarboxylic Acids; B. 3-Benzofurancarboxylic Acids; C. Hydroxybenzofurancarboxylic Acids; 2. Benzofuran Dicarboxylic Acids; 3. Benzofuranylalkanoic Acids; A. Benzofuranylacetic Acids; B. Benzofuranylpropionic Acids; C. Benzofuranylbutyric Acids; D. Miscellaneous Benzofuranylalkanoic Acids
4. Miscellaneous Reactions of Benzofurancarboxylic AcidsA. Halogenation; B. Chloromethylation; C. Nitration; D. Saponification; E. Catalytic Hydrogenation; F. Peroxide Formation and Ozonolysis; G. Acylation; H. Alkylation; I. Miscellaneous Reactions; References; IV. Hydrogenated Benzofurans; 1. Dihydrobenzofurans; A. Alkyl- (or Aryl-) Substituted 2.3-Dihydrobenzofurans; B. Halogen-Substituted 2,3-Dihydrobenzofurans; C. Nitro-Substituted 2,3-Dihydrobenzofurans; D. Amino-Substituted 2,3-Dihydrobenzofurans; E. 2.3-Dihydrobenzofuranols; F. Geometrical Isomers of 2,3-Dihydrobenzofurans
G. Miscellaneous Reactions of 2,3-Dihydrobenzofurans
Chemistry of Heterocyclic Compounds publishes articles, letters to the Editor, reviews, and minireviews on the synthesis, structure, reactivity, and biological activity of heterocyclic compounds including natural products. The journal covers investigations in heterocyclic chemistry taking place in scientific centers of all over the world, including extensively the scientific institutions in Russia, Ukraine, Latvia, Lithuania and Belarus.