Chemical and Pharmaceutical Bulletin p. 955 - 959 (1995)
Update date:2022-09-26
Topics:
Maruyama
Utsumi
Tomioka
Kasamoto
Sato
Anne
De Clercq
A procedure for the synthesis of 2'-deoxy-2'-fluoropuromycin (1b) was developed. Ring opening of the lyxo-epoxide (4) or nucleophilic displacement of the 3'-O-mesylate (5) by an azide ion afforded two azido nucleosides, 6a and 7a. The major product (7a) w
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Doi:10.1021/jo00116a027
(1995)Doi:10.1016/0040-4039(94)88270-3
(1994)Doi:10.1080/10426509808032471
(1998)Doi:10.1080/00397911.2020.1802758
(2020)Doi:10.1021/ja973832e
(1998)Doi:10.1002/cber.19681010934
(1968)