1.

Record Nr.

UNINA9910144283303321

Autore

Mustafa Ahmed <1918->

Titolo

Furopyrans and furopyrones [[electronic resource] /] / Ahmed Mustafa

Pubbl/distr/stampa

London ; ; New York, : Interscience Publishers, 1967

ISBN

1-282-30163-2

9786612301636

0-470-18687-9

0-470-18835-9

Edizione

[99th ed.]

Descrizione fisica

1 online resource (391 p.)

Collana

The chemistry of heterocyclic compounds ; ; 23

Disciplina

547/.59/05

Soggetti

Furopyran

Furopyranone

Electronic books.

Lingua di pubblicazione

Inglese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Note generali

Description based upon print version of record.

Nota di bibliografia

Includes bibliographies.

Nota di contenuto

FUROPYRANS 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

P. 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

II. 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

II. 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)

B. 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

IX. Physiological Activity

Sommario/riassunto

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.