A hypodiboric acid system for the reduction of nitro groups on DNA–chemical conjugates has been developed. This transformation provided good to excellent yields of the reduced amine product for a variety of functionalized aromatic, heterocyclic, and aliphatic nitro compounds. DNA tolerance to reaction conditions, extension to decigram scale reductions, successful use in a DNA-encoded chemical library synthesis, and subsequent target selection are also described
DNA-encoded libraries (DELs) are an increasingly popular approach to finding small molecule ligands ...
672-673Aromatic azoxy compounds have been prepared in good yields by the selective reduction of aro...
The limited scope of DNA-compatible chemistry restricts the types of chemical features that can be i...
DNA-encoded chemical libraries have emerged as a cost-effective alternative to high-throughput scree...
We have demonstrated a scalable chemoselective reduction of a nitro functional group in the presence...
The reduction of the nitro group represents a powerful and widely used transformation that allows to...
DNA-encoded chemical libraries are collections of small molecules, attached to DNA fragments serving...
© 2017 The Chemical Society of Japan.Biologically relevant amines react with acrolein to provide 3-f...
75-77Aliphatic and aromatic nitro compounds are selectively and rapidly reduced to their correspond...
A new, mild, metal-free, HSiCl3-mediated reduction of both aromatic and aliphatic nitro groups to am...
A new, mild, metal-free, HSiCl<sub>3</sub>-mediated reduction of both aromatic and aliphatic nitro g...
NRs are enzymes that catalyze the reduction of nitroaromatics to their corresponding nitroso, hydrox...
Chemoselective reduction of activated carbon-carbon double bond in conjugated nitroalkenes was achie...
Aliphatic and aromatic nitro compounds are selectively and rapidly reduced to their corresponding am...
A new simple methodology for DNA conjugation or staining was developed. 2′-Deoxyribonucleoside trip...
DNA-encoded libraries (DELs) are an increasingly popular approach to finding small molecule ligands ...
672-673Aromatic azoxy compounds have been prepared in good yields by the selective reduction of aro...
The limited scope of DNA-compatible chemistry restricts the types of chemical features that can be i...
DNA-encoded chemical libraries have emerged as a cost-effective alternative to high-throughput scree...
We have demonstrated a scalable chemoselective reduction of a nitro functional group in the presence...
The reduction of the nitro group represents a powerful and widely used transformation that allows to...
DNA-encoded chemical libraries are collections of small molecules, attached to DNA fragments serving...
© 2017 The Chemical Society of Japan.Biologically relevant amines react with acrolein to provide 3-f...
75-77Aliphatic and aromatic nitro compounds are selectively and rapidly reduced to their correspond...
A new, mild, metal-free, HSiCl3-mediated reduction of both aromatic and aliphatic nitro groups to am...
A new, mild, metal-free, HSiCl<sub>3</sub>-mediated reduction of both aromatic and aliphatic nitro g...
NRs are enzymes that catalyze the reduction of nitroaromatics to their corresponding nitroso, hydrox...
Chemoselective reduction of activated carbon-carbon double bond in conjugated nitroalkenes was achie...
Aliphatic and aromatic nitro compounds are selectively and rapidly reduced to their corresponding am...
A new simple methodology for DNA conjugation or staining was developed. 2′-Deoxyribonucleoside trip...
DNA-encoded libraries (DELs) are an increasingly popular approach to finding small molecule ligands ...
672-673Aromatic azoxy compounds have been prepared in good yields by the selective reduction of aro...
The limited scope of DNA-compatible chemistry restricts the types of chemical features that can be i...