The structural study of internal [2+2] photodimers of the derivatives of 1,1′-trimethylene-bis-(5-fluoro) uracil

The structure of internal [2+2] photodimers of 1,1′-trimethylene-bis-(5-fluoro) uracil derivatives has been studied. All investigated compounds have cis-syn geometry with puckered endocyclic cyclobutane ring and chair-like conformation of 1,3-diazacycloheptane ring.

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Bibliographische Detailangaben
Veröffentlicht in:	Biochemical and biophysical research communications 1987-08, Vol.146 (3), p.1270-1276
Hauptverfasser:	Koroniak, H., Wójtowicz, H., Golankiewicz, K.
Format:	Artikel
Sprache:	eng
Schlagworte:	Applied sciences Exact sciences and technology Fluorouracil - analogs & derivatives Hydrogen-Ion Concentration Magnetic Resonance Spectroscopy Models, Molecular Nucleic Acid Conformation Other techniques and industries Photochemistry Quantum Theory Structure-Activity Relationship
Online-Zugang:	Volltext
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Beschreibung
Zusammenfassung:	The structure of internal [2+2] photodimers of 1,1′-trimethylene-bis-(5-fluoro) uracil derivatives has been studied. All investigated compounds have cis-syn geometry with puckered endocyclic cyclobutane ring and chair-like conformation of 1,3-diazacycloheptane ring.
ISSN:	0006-291X 1090-2104
DOI:	10.1016/0006-291X(87)90785-6