Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Yunyun, Ning"'
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-9 (2021)
Catalytic amide bond-forming methods is important because they could potentially address the existing limitations of classical methods using superstoichiometric activating reagents. Here the authors show an Umpolung amidation reaction of carboxylic a
Externí odkaz:
https://doaj.org/article/d3ce2c10fd0d492db89ee66b2fb0d294
Publikováno v:
Analytica chimica acta. 1223
Accurate detection of microRNA (miRNA) is challenging but essential for disease diagnostics and therapeutics. To meet the high demands of miRNA analysis, we proposed a highly sensitive and specific electrochemical strategy based on duplex-specific nu
Publikováno v:
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-9 (2021)
Nature Communications, Vol 12, Iss 1, Pp 1-9 (2021)
Development of catalytic amide bond-forming methods is important because they could potentially address the existing limitations of classical methods using superstoichiometric activating reagents. In this paper, we disclose an Umpolung amidation reac
Publikováno v:
Chem. 5:2718-2730
Summary The biaryl coupling between a nucleophile (Arδ−: arylboronates or arylsilanes) and an electrophile (Arδ+: arylhalides) represents the state of the art in carbon–carbon bond formation. The intrinsic functional-group limitations in these
Publikováno v:
Chemical Science
In this paper, we report a mild and practical method for precise deuteration of aliphatic carboxylic acids by synergistic photoredox and HAT catalysis. The reaction delivers excellent D-incorporation (up to 99%) at predicted sites even in substrates
Publikováno v:
SSRN Electronic Journal.
Synthesis of biaryls by Suzuki-Miyaura or Hiyama coupling represents the-state-of-art in carbon-carbon bond formation, in which the coupling occurs between a nucleophile (Arδ-: arylboronates or arylsilanes) and an electrophile (Arδ+: arylhalides).