Journal of Medicinal Chemistry p. 684 - 691 (1976)
Update date:2022-08-03
Topics:
Chang
Coward
The synthesis of S adenosylhomocysteine analogues, in which the 5' thioether linkage is replaced by an oxygen or nitrogen isostere, has been investigated. These compounds were designed to be resistant to enzyme catalyzed hydrolytic cleavage of the 5' subs
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(1999)Doi:10.1016/S0040-4039(00)87712-6
(1982)Doi:10.1021/acs.orglett.6b01059
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(1976)Doi:10.1021/ja01193a041
(1947)
