The enzymatic substrate inhibition pattern was followed in the catalytic aerobic oxidation of 3,5-di-tert-butylcatechol (DTBC) in methanol utilising cyclic hindered base. The primary mechanistic finding for this aerobic oxidation was the r...
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Photosulfonylation of Aryl Halides with Sodium Sulfinates Catalyzed by Heterogeneous Copper Polymers
Von Wiley-VCH zur Verfügung gestellt
Heterogeneous HCPs-Cu were readily prepared by using direct knitting strategy, which enabled a general photocatalytic method for sulfonylation of aryl halides with sodium sulfinates. Besides the remarkably broad substrate scope (43 examples), and a moderate reusability (10 times) were proved.
Abstract
A general method for photosulfonylation of aryl halides with sodium sulfinates was successfully developed by using reusable copper-containing hyper-cross-linked polymers (HCPs-Cu). These heterogeneous catalysts were easily prepared from molecular BINAP/Cu(MeCN)4PF6 complex (BINAP-Cu) with different amounts of benzene and formaldehyde dimethyl acetal (FDA) via direct knitting strategy, and the Cu center was uniformly dispersed in the matrices of HCPs-Cu, featuring the same coordination environment to that of molecular BINAP-Cu. This photosulfonylation system not only tolerates a wide range of substrates to furnish aryl sulfones, showing a potential in the synthesis of several drugs, but also highlights a moderate recyclability of 10 runs with minimal loss of catalytic activity.
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