LEADER 05127nam 2200637Ia 450 001 9910830143703321 005 20230213211353.0 010 $a1-282-30163-2 010 $a9786612301636 010 $a0-470-18687-9 010 $a0-470-18835-9 035 $a(CKB)1000000000376543 035 $a(EBL)469743 035 $a(OCoLC)814417522 035 $a(SSID)ssj0000353969 035 $a(PQKBManifestationID)11260961 035 $a(PQKBTitleCode)TC0000353969 035 $a(PQKBWorkID)10302051 035 $a(PQKB)10215410 035 $a(MiAaPQ)EBC469743 035 $a(EXLCZ)991000000000376543 100 $a20780510d1967 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aFuropyrans and furopyrones$b[electronic resource] /$fAhmed Mustafa 205 $a99th ed. 210 $aLondon ;$aNew York $cInterscience Publishers$d1967 215 $a1 online resource (391 p.) 225 1 $aThe chemistry of heterocyclic compounds ;$v23 300 $aDescription based upon print version of record. 311 $a0-470-38202-3 320 $aIncludes bibliographies. 327 $aFUROPYRANS and FUROPYRONES; Contents; I. Fumpyrans and -pyronea; I. Naturally Occurring Furopyrms; 1. Plumericin; 2. Anhydrotetrahydroaucubigenin; II. Synthetic Furopyrans and -pyrones; III. References; II. Furocoumorins; I. Isolation; II. Physical Properties; III. Nomenclature; IV. Naturally Occurring Furocoumarins; 1. Structure and Chemicd Properties; A. Angelicin; B. Psoralen; C. Bergapten; D. Bergaptol; E. Isobergapten.; F. Bergamuttin.; G. Xanthotoxin; H. Xanthotoxol; I. Isoimperetorin; J. Oxypeucedanin; K. ostruthol; L. Imperstorin; M. Alloimperatorin; N. Herdenin; O. Isopimpinellin 327 $aP. PhellopterinQ. Byekangelicol; R. Byakangelicin; S. Pimpinellin; T. Sphondin; U. Halfordin and Isohalfordm; V. Nodakenetin.; W. Peucedanin; X. Athamantin; Y. Discophoridin; Z. Edultin; AA.Peulustrin; BB. Columbiansdin and Columbisnin; CC. Archangelicin; DD. Archangelin; EE. Pyrocanescin; FF. 4,5',8-Trimethylpralen; GG. Aflatoxins B and G; 2. Configuration; 3. Biosynthesia; A. a-(B'-Hydroxypropyl)dihydrofurans and a-Lsopropenyl-dihydrofurans; B. a-Isopropyl-B--hydroxyfurans and Relations; C. Simple Furans; 4. Physiological Activity; V. References; III. Furochromones; I. Isolation 327 $aII. Physical PropertiesIII. Nomenclature; IV. Naturally Occurring Furochromones; 1. Chemical Properties; A. Khellin; (1) synthesis of khellin; (2) Synthesis of khellin analogs; (3) Reactions; B. Visnagin; (1) synthesis of visnagin; (2) Syntheeis of visnagin analogs and related transformations; (3) Reactions; C. Khellinol; D.Khellinin; E. Khellol; F. Anamiol; G. Visanminol; 2. Color Reactions; 3. Physiological Activity; V. References; IV.Furoxanthones; I. Naturally Occurring Furoxanthones; 1. Sterigmatocystin; II. Synthetic Furoxanthones; III. References; V. Furoflavones; I. Isolation 327 $aII. Physical PropertiesIII. Naturdy Occurring Furoflavones; 1. chemical Properties; A. Karanjin; B. Lanceolatin B; C. Pongapin; D. Kenjone; E. Pongaglabrone; F.Atanasin; G. Gamatin; H. Pinnatin; IV. Synthetic Furoflavones; 1. Linear-type; 2. Angular-type; V. References; VI. Furoisoflavanoids; I. Introduction; II. Furoisoflavanones; 1. Naturally Occurring Furoisoflavenones; A. Nepseudin; B. Neotenone; 2. Synthetic Fuarioflavanones; A. Angular Furoisoflavones; (1) Introduction of a furan nucleus into an isoflavone skeleton (Tanaka's method); (2) Ethyl orthoformate method (Venkataraman) 327 $aB. Linear Furo(3"",2""-6,7)isoflavonesIII. Coumaranochromans; 1. Introduction; 2. Naturally Occurring Coumaranochromans; A. Homopterocarpin; B. Pterocarpin; C. Maackiain; D. Pisatin; E. Neodulin; F.Phaseollin; IV. Coumaronoflavan-4-ols; 1. NaturalIy Occurring Coumamnoflavan-4-ols; A. Cyanomaclurin; 2. Synthetic 11H-benzofuro(3,2-b)-1-benzopyran-11-ones; V. Coumaronocoumarins; 1. Naturally Occurring Coumaronocoumarins; A. Coumestrol; B. Wedelolactone; C. Trifoliol; D. Medicagol; E. Psoralidin; VI. 3-Arylfurocoumarins; VII. Coumaronofurocoumarins; VIII. Furo(3,2-c)-1-benzopyran-4-ones 327 $aIX. Physiological Activity 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 ;$v23. 606 $aFuropyran 606 $aFuropyranone 615 4$aFuropyran. 615 4$aFuropyranone. 676 $a547/.59/05 700 $aMustafa$b Ahmed$f1918-$0911772 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830143703321 996 $aFuropyrans and furopyrones$92041743 997 $aUNINA