Skip navigation
Skip navigation

Direct Cross-Couplings of Propargylic Diols

Green, Nicholas J; Willis, Anthony C; Sherburn, Michael


[Pd(PPh3 )4 ] catalyzes a Suzuki-Miyaura-like twofold cross-coupling sequence between underivatized propargylic diols and either aryl or alkenyl boronic acids to furnish highly substituted 1,3-dienes. Thus, 2,3-diaryl-1,3-butadienes and their dialkenic congeners ([4]dendralenes) are delivered in a (pseudo)halogen-free, single-step synthesis which supersedes existing methods. Allenols are also readily formed. Treatment of these single- and twofold cross-coupled products with acid leads to...[Show more]

CollectionsANU Research Publications
Date published: 2016-08-01
Type: Journal article
Source: Angewandte Chemie (International ed. in English)
DOI: 10.1002/anie.201604527
Access Rights: Open Access


There are no files associated with this item.

Items in Open Research are protected by copyright, with all rights reserved, unless otherwise indicated.

Updated:  19 May 2020/ Responsible Officer:  University Librarian/ Page Contact:  Library Systems & Web Coordinator