6456-93-5Relevant articles and documents
Light-induced [2 + 2] cycloadditions for the construction of cyclobutane-fused pyridinyl sulfonyl fluorides
Liu, Jing,Wang, Shi-Meng,Qin, Hua-Li
supporting information, p. 4019 - 4023 (2020/06/09)
Cyclobutanes are an important class of motifs present in a wide range of natural products and other biologically significant molecules. A photocatalytic [2 + 2] cycloaddition between pyridones or isoquinolones and ethenesulfonyl fluoride was achieved, providing a portal to a class of unique cyclobutane-fused pyridinyl sulfonyl fluorides with quaternary rigid rings (30 examples). Further applications of these novel sulfonyl fluoride molecules in SuFEx click chemistry were also accomplished, providing the corresponding sulfonates and sulphonamides with reasonable yields.
Direct alkenylation and alkylation of pyridone derivatives by Ni/AlMe 3 catalysis
Nakao, Yoshiaki,Idei, Hiroaki,Kanyiva, Kyalo Stephen,Hiyama, Tamejiro
supporting information; experimental part, p. 15996 - 15997 (2010/02/16)
(Chemical Equation Presented) Regioselective alkenylation and alkylation of 2-pyridone derivatives are achieved through inter- and intramolecular insertion of alkynes, 1,3-dienes, and alkenes into the C(6)-H bond by nickel/AlMe 3 catalysis. Coo
Reactions of 1-unsubstituted tautomeric 2-pyridones with benzyne
Kuzuya,Noguchi,Kamiya,Okuda
, p. 2313 - 2322 (2007/10/02)
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