Two (E,E)- and (Z,E)-thiazol-5-ylpenta-2,4-dienones.
نویسندگان
چکیده
In order to characterize the structural elements that might play a role in non-covalent DNA binding by the antitumor antibiotic leinamycin, we have solved the crystal structures of the two leinamycin analogs, methyl (R)-5-[2-[1-(tert-butoxycarbonylamino)ethyl]thiazol-4-yl]penta-(E,E)-2,4-dienoate, C(16)H(22)N(2)O(4)S, (II), and 2-methyl-8-oxa-16-thia-3,17-diazabicyclo[12.2.1]heptadeca-(Z,E)-1(17),10,12,14-tetraene-4,9-dione, C(14)H(16)N(2)O(3)S, (III). The penta-2,4-dienone moiety in both of these analogs adopts a conformation close to planarity, with the thiazole ring twisted out of the plane by 12.9 (2) degrees in (II) and by 21.4 (4) degrees in (III).
منابع مشابه
Photolysis of Aromatic Ethers
H e i n z P e t e r S c h u c h m a n n a n d C l e m e n s v o n S o n n t a g * Institut für Strahlenchemie im Max-Planck-Institut für Kohlenforschung, Stiftstraße 34-36, D-4330 Mülheim a. d. Ruhr Dedicated, to Professer Oskar E. Polansky on the occasion of his 60th anniversary Z. Naturforsch. 84b, 1002-1009 (1979); received February 23, 1979 !H NMR, Photo-CIDNP, Photolysis of Aryl Ethers, Ke...
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عنوان ژورنال:
- Acta crystallographica. Section C, Crystal structure communications
دوره 58 Pt 8 شماره
صفحات -
تاریخ انتشار 2002