LEADER 05175nam 2200673Ia 450 001 9910144280803321 005 20170815154012.0 010 $a1-282-30174-8 010 $a9786612301742 010 $a0-470-18699-2 010 $a0-470-18850-2 035 $a(CKB)1000000000376555 035 $a(EBL)469742 035 $a(OCoLC)814417516 035 $a(SSID)ssj0000357066 035 $a(PQKBManifestationID)11277648 035 $a(PQKBTitleCode)TC0000357066 035 $a(PQKBWorkID)10366889 035 $a(PQKB)11286489 035 $a(MiAaPQ)EBC469742 035 $a(PPN)248180460 035 $a(EXLCZ)991000000000376555 100 $a20080921d1974 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aBenzofurans$b[electronic resource] 205 $a99th ed. 210 $aNew York $cWiley$d1974 215 $a1 online resource (538 p.) 225 1 $aThe Chemistry of heterocyclic compounds ;$vv. 29 300 $aDescription based upon print version of record. 311 $a0-471-38207-8 320 $aIncludes bibliographical references. 327 $aFront 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 327 $al. 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 327 $aD. 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 327 $aC. 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 327 $a4. 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 327 $aG. Miscellaneous Reactions of 2,3-Dihydrobenzofurans 330 $aChemistry of Heterocyclic Compounds publishes articles, letters to the Editor, reviews, and minireviews on the synthesis, structure, reactivity, and biological activity of heterocyclic compounds including natural products. The journal covers investigations in heterocyclic chemistry taking place in scientific centers of all over the world, including extensively the scientific institutions in Russia, Ukraine, Latvia, Lithuania and Belarus. 410 0$aChemistry of heterocyclic compounds ;$vv. 29. 606 $aBenzofuran 606 $aHeterocyclic compounds 615 0$aBenzofuran. 615 0$aHeterocyclic compounds. 676 $a547.592 676 $a547/.59/05 676 $a547/.592 700 $aMustafa$b Ahmed$f1918-$0911772 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910144280803321 996 $aBenzofurans$92179696 997 $aUNINA LEADER 01606nam 2200337Ia 450 001 996395423503316 005 20221107225145.0 035 $a(CKB)4330000000322768 035 $a(EEBO)2248519237 035 $a(OCoLC)13142499 035 $a(EXLCZ)994330000000322768 100 $a19860212d1641 uy | 101 0 $aeng 135 $aurbn||||a|bb| 200 13$aAn act made by the Estates of Parliament conveened by His Maiesties speciall authority, and holden at Edenburgh in Scotland, anno 1641$b[electronic resource] $edeclaring all Episcopall governement, the civill places and power of kirk-men, the late service booke, booke of cannons and ordination, the High Commission, together with the Articles of Perth for the observation of festivall dayes, kneeling at the communion, &c. to bee utterly unlawfull and still rejected in that kirke and kingdome : whereunto is added an act appointing Parliaments to be held every three yeares 210 $aEdenburg $cPrinted by I.B. ;$aand now printed at London $cfor J.W.I.$d1641 215 $a[2], 6 p 300 $aReproduction of original in Duke University Library. 330 $aeebo-0040 606 $aChurch and state$zScotland$vEarly works to 1800 615 0$aChurch and state 712 02$aScotland.$bParliament. 801 0$bEAA 801 1$bEAA 801 2$bm/c 801 2$bEAA 801 2$bWaOLN 906 $aBOOK 912 $a996395423503316 996 $aAn act made by the Estates of Parliament conveened by His Maiesties speciall authority, and holden at Edenburgh in Scotland, anno 1641$92365168 997 $aUNISA