Pd-catalyzed atom-efficient cross-coupling of triarylbismuth reagents with protecting group-free iodophenylmethanols: Synthesis of biarylmethanols

[Display omitted] •An efficient atom-efficient synthesis of functionalized biarylmethanols.•Pd-catalyzed cross-couplings using iodophenylmethanols.•Atom-economic triarylbismuth reagents.•Protecting group-free couplings and synthesis. An atom-efficient procedure for the synthesis of functionalized bi...

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Bibliographic Details
Published in:Tetrahedron letters Vol. 61; no. 13; p. 151676
Main Authors: Rao, Maddali L.N., Meka, Suresh
Format: Journal Article
Language:English
Published: Elsevier Ltd 26-03-2020
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Summary:[Display omitted] •An efficient atom-efficient synthesis of functionalized biarylmethanols.•Pd-catalyzed cross-couplings using iodophenylmethanols.•Atom-economic triarylbismuth reagents.•Protecting group-free couplings and synthesis. An atom-efficient procedure for the synthesis of functionalized biarylmethanols via the Pd-catalyzed cross-coupling reactions of differently functionalized iodophenylmethanols and triarylbismuth reagents is described. This protecting group-free direct couplings of 2-, 3- or 4-iodophenylmethanols with triarylbismuth reagents afforded biarylmethanols in good to high yields.
ISSN:0040-4039
1873-3581
DOI:10.1016/j.tetlet.2020.151676