Journal
CHEMICAL COMMUNICATIONS
Volume 54, Issue 12, Pages 1497-1500Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7cc08715b
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Funding
- National Natural Science Foundation of China [21432008, 21721005, 91753201]
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An azide and hydrazine tethered to a naphthalimide analogue was created to selectively react with 5-formyluracil in one system and fluorogenically label 5-formylcytosine in another system. A biotin group was also introduced by copper-free click chemistry through selective labelling of the aldehyde present in 5-formylpyrimidine.
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