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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Published in: | Tetrahedron letters Vol. 61; no. 13; p. 151676 |
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Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
Elsevier Ltd
26-03-2020
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Subjects: | |
Online Access: | Get full text |
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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. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2020.151676 |