LEADER 01134nam2-2200361---450 001 990001714100203316 005 20220420112638.0 035 $a000171410 035 $aUSA01000171410 035 $a(ALEPH)000171410USA01 035 $a000171410 100 $a20040531d1982----km-y0itay0103----ba 101 0 $aeng 102 $aSE 105 $aa|||||||001yy 200 1 $a1.3. : Temple of Zeus$fby Pontus Hellström and Thomas Thieme 210 $aLund$cGleerup$d1982 215 $a110 p.$cill.$d30 cm 225 2 $aSkrifter utgivna av Svenska institutet i Athen$v5 300 $aIn testa al frontespizio: Svenska forskningsinstitutet i Instanbul. Swedish research institute in Instanbul 410 0$12001$aSkrifter utgivna av Svenska institutet i Athen$v5 454 1$12001 461 1$1001000171392$12001$aLabraunda 676 $a939 702 1$aHELLSTRÖM,$bPontus 702 1$aTHIEME,$bThomas 801 0$aIT$bsalbc$gISBD 912 $a990001714100203316 951 $aXI.3.B. 88/1.3(X B 201/1 III)$b23081 L.M.$cX B 959 $aBK 969 $aUMA 996 $a1.3. : Temple of Zeus$92831046 997 $aUNISA LEADER 05161nam 2200649Ia 450 001 9910144283303321 005 20220808173829.0 010 $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. 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