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Improving foldamer synthesis through protecting group induced unfolding of aromatic oligoamides. | LitMetric

The hydrogen bond rigidified backbones of aromatic oligoamides are temporarily interrupted by replacing the amide hydrogens with the acid-labile 2,4-dimethoxybenzyl (DMB) group, which allows the efficient preparation of long folding oligomers that, upon removal of the DMB groups, fold into multiturn helices. [structure: see text]

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Source
http://dx.doi.org/10.1021/ol062103dDOI Listing

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