The Synthesis of 5,11,17‐Trihalotetracyclo [13.3.1.1 3,7 .1 9,13 ]henicosa‐1 (19),3,5,7 (20),9,11,13 (21), 15,17‐nonaene‐19,20,21‐triols and 5,11,17‐trihalo‐19,20,21‐trihydroxytetracyclo [13.3.1.1 3,7 . 1 9,13 ]henicosa‐1 (19),3,5,7 (20),9,11,13(21), 15,17‐nonaene‐8,14‐dione [1]. Cyclo‐derivatives of Phloroglucide Analogues | Zendy

Moshfegh Ali A. | Zendy; Beladi Effat | Zendy; Radnia Lida | Zendy; Hosseini Afsaneh S. | Zendy; Tofigh Soosan | Zendy; Hakimelahi Gholam H. | Zendy

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The Synthesis of 5,11,17‐Trihalotetracyclo [13.3.1.1 3,7 .1 9,13 ]henicosa‐1 (19),3,5,7 (20),9,11,13 (21), 15,17‐nonaene‐19,20,21‐triols and 5,11,17‐trihalo‐19,20,21‐trihydroxytetracyclo [13.3.1.1 3,7 . 1 9,13 ]henicosa‐1 (19),3,5,7 (20),9,11,13(21), 15,17‐nonaene‐8,14‐dione [1]. Cyclo‐derivatives of Phloroglucide Analogues

Author(s) -

Moshfegh Ali A.,

Beladi Effat,

Radnia Lida,

Hosseini Afsaneh S.,

Tofigh Soosan,

Hakimelahi Gholam H.

Publication year - 1982

Publication title -

helvetica chimica acta

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.74

H-Index - 82

eISSN - 1522-2675

pISSN - 0018-019X

DOI - 10.1002/hlca.19820650416

Subject(s) - chemistry , in vitro , stereochemistry , biochemistry

The synthesis of the title compounds ( 1 and 3 ) is described. Some of the compounds prepared were found to be active against a number of pathogenic microorganisms in vitro. Structure‐activity relationship is briefly discussed.

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