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Beilstein J. Org. Chem. 2018, 14, 397–406, doi:10.3762/bjoc.14.28
Graphical Abstract
Figure 1: Preparation of fully protected trinucleotides in solution (A), on solid phase (B) and on soluble po...
Figure 2: Strategies for trinucleotide synthesis using different pairs of orthogonal groups for protection of...
Figure 3: Strategy for the synthesis of nucleotide dimers and extension to the trimer in either 5'- or 3'-dir...
Figure 4: Removal of the 3'-O-protecting group under conditions that leave all other protecting groups at 5'-...
Figure 5: Release of trinucleotide blocks from the solid support by cleavage of an oxalyl anchor (A) and by a...
Figure 6: Release of the trinucleotide from the support under reductive conditions.
Figure 7: Phosphitylation of trimers. Reaction conditions, in particular the choice of the phosphitylation re...