Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bokyeong, Ryou"'
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-12 (2020)
[2 + 2] cycloaddition of alkynes with alkenes would normally require UV light irradiation. Here, the authors report an alkyne–alkene [2 + 2] cycloaddition based on visible light energy transfer photocatalysis, both inter- and intramolecularly, to a
Externí odkaz:
https://doaj.org/article/6bc8f7e905284ef1bc6beb5c43d30257
Publikováno v:
Organic & Biomolecular Chemistry. 21:585-589
An efficient method for the synthesis of both symmetrically and unsymmetrically substituted dithioacetals from vinyl sulfides.
Publikováno v:
Organic Letters. 24:4264-4269
Synthesis of Bicyclic N-Heterocycles via Photoredox Cycloaddition of Imino-Alkynes and Imino-Alkenes
Publikováno v:
ACS Catalysis. 11:13670-13679
Publikováno v:
Organic letters. 24(23)
We describe the electrochemical α-amidoalkylation of γ-lactams based on transition-metal-free cross-coupling via hydrogen atom transfer. The highly selective hydrogen atom transfer process allows for a broad substrate scope including both inter- an
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-12 (2020)
Nature Communications
Nature Communications
UV-activated alkyne–alkene [2 + 2] cycloaddition has served as an important tool to access cyclobutenes. Although broadly adopted, the limitations with UV light as an energy source prompted us to explore an alternative method. Here we report alkyne