6412-93-7Relevant articles and documents
Catalytic Aldehyde and Alcohol Arylation Reactions Facilitated by a 1,5-Diaza-3,7-diphosphacyclooctane Ligand
Isbrandt, Eric S.,Nasim, Amrah,Newman, Stephen G.,Zhao, Karen
supporting information, p. 14646 - 14656 (2021/09/18)
We report a catalytic method to access secondary alcohols by the coupling of aryl iodides. Either aldehydes or alcohols can be used as reaction partners, making the transformation reductive or redox-neutral, respectively. The reaction is mediated by a Ni catalyst and a 1,5-diaza-3,7-diphosphacyclooctane. This P2N2ligand, which has previously been unrecognized in cross-coupling and related reactions, was found to avoid deleterious aryl halide reduction pathways that dominate with more traditional phosphines and NHCs. An interrupted carbonyl-Heck type mechanism is proposed to be operative, with a key 1,2-insertion step forging the new C-C bond and forming a nickel alkoxide that may be turned over by an alcohol reductant. The same catalyst was also found to enable synthesis of ketone products from either aldehydes or alcohols, demonstrating control over the oxidation state of both the starting materials and products.
Regioselective annulation of 5-(1-alkenyl)- and 5-vinyl-1,3-benzodioxoles with 3-chloro-3-cyclobutene-1,2-dione. Synthesis of 3,4-dihydrocyclobuta[5,6]-naphtho[2,3-d][1,3]dioxole-1,2-diones and cyclobuta[5,6]naphtho[2,3-d][1,3]dioxole-1,2-diones
Schmidt,Kircher,Kunz,Wahl,Hendriok
, p. 3890 - 3894 (2007/10/02)
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