1.
Helv Chim Acta
; 58(6): 1735-8, 1975 Sep 24.
Article
in French
| MEDLINE
| ID: mdl-1176302
2.
Ann N Y Acad Sci
; 255: 151-65, 1975 Aug 08.
Article
in English
| MEDLINE
| ID: mdl-1059351
ABSTRACT
We have developed general methods for the synthesis of 4'-fluoro- and 4'-methoxynucleosides by addition of iodinemonofluoride or iodine and methanol across the double bond of suitably protected 4',5'-unsaturated pyrimidine and purine nucleosides. The structures of these adducts have been determined by a combination of chemical, spectroscopic, and electrophoretic methods. The 4'-methoxy- and the uridine analogs of nucleocidin have been synthesized from the corresponding 4'-fluorouridine and 4'-methoxyadenosine derivatives.
Subject(s)
Nucleosides/chemical synthesis , Adenosine/analogs & derivatives , Cytidine/analogs & derivatives , Fluorine , Iodine , Methods , Molecular Conformation , Structure-Activity Relationship , Uridine/analogs & derivatives
3.
Helv Chim Acta
; 53(6): 1484-9, 1970.
Article
in French
| MEDLINE
| ID: mdl-5482377
4.
Helv Chim Acta
; 52(8): 2569-73, 1969.
Article
in French
| MEDLINE
| ID: mdl-5361921