Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5271080 | Tetrahedron Letters | 2014 | 5 Pages |
Abstract
A novel class of 5â²-amino-2â²,5â²-dideoxy-2â²,2â²-difluorocytidine derivatives has been synthesized in order to identify anticancer nucleoside analogs. Several synthetic routes were devised and implemented which relied upon either SN2 displacement or reductive amination to provide the desired derivatives.
Graphical abstractA novel series of 5â²-amino-2â²,5â²-dideoxy-2â²,2â²-difluorocytidine derivatives, represented by 1, have been prepared via three different synthetic routes in order to profile them as potential anticancer agents.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Marc A. Labroli, Michael P. Dwyer, Ruichao Shen, Janeta Popovici-Muller, Qinglin Pu, Judson Richard, Kristen Rosner, Kamil Paruch, Timothy J. Guzi,