| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5280106 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
A synthesis of the enantiomer of nelarabine is described. Subtle changes in the protecting group strategy allow for an efficient inversion of the C-2â² stereocentre.
Graphical abstractA synthesis of the enantiomer of nelarabine is described. Subtle changes in the protecting group strategy allow for an efficient inversion of the C-2â² stereocentre.Download full-size image
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Karim Herbal, John Kitteringham, Martyn Voyle, Andrew J. Whitehead,