DNA-templated functional group transformations enable sequence-programmed synthesis using small-molecule reagents.

J Am Chem Soc
Authors
Keywords
Abstract

DNA-templated organic synthesis (DTS) has previously been used primarily to direct coupling reactions between two DNA-linked reactants. In some cases, reactants are difficult or impossible to tether to DNA oligonucleotides. The development of strategies that enable non-DNA linked small-molecule reagents to participate in sequence-programmed synthesis therefore would significantly expand the capabilities of DTS. We developed efficient DNA-templated functional group transformations of template-linked azides into corresponding amines, carboxylic acids, and thiols. The application of these reactions to a single-solution mixture of four template-linked organic azides enabled each azide to be transformed sequence specifically into a sulfonamide, carbamate, urea, or thiourea using small-molecule sulfonyl chloride, chloroformate, isocyanate, or isothiocyanate reagents not tethered to DNA. Only the four desired products were observed, without formation of any of the 12 possible undesired cross-products. Our results represent a new approach to small molecule diversification in a DNA-programmed manner.

Year of Publication
2005
Journal
J Am Chem Soc
Volume
127
Issue
6
Pages
1660-1
Date Published
2005 Feb 16
ISSN
0002-7863
DOI
10.1021/ja0432315
PubMed ID
15700999
Links
Grant list
R01 GM 065865 / GM / NIGMS NIH HHS / United States