Beilstein J. Org. Chem.2019,15, 1116–1128, doi:10.3762/bjoc.15.108
protections, which contained a tertiarybutylcarbamate moiety, were not completely stable under the acidic conditions needed for de-tritylation in each synthetic cycle. Once the protection was lost, in the coupling step, incoming phosphoramidites would react with the free amino groups, and branched ODNs
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Graphical Abstract
Scheme 1:
Comparison of Dmoc and dM-Dmoc as nucleobase protecting groups for ODN synthesis.
Beilstein J. Org. Chem.2009,5, No. 66, doi:10.3762/bjoc.5.66
; tertiarybutylcarbamate; tertiary butyl carbazate; α,β-unsaturated ketone; Introduction
Pyrrolopyridazine derivatives have various biological applications [1][2][3][4][5][6][7][8], and their fluorescent properties have been investigated for potential use in sensors, lasers, and semiconductor devices [9