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Tandem nucleophilic addition-Oppenauer oxidation of aromatic aldehydes to aryl ketones with triorganoaluminium reagents

journal contribution
posted on 2024-11-01, 13:15 authored by Ying Fu, Yanshou Yang, Helmut Hugel, Zhengyin Du, Kehu Wang, Danfeng Huang, Yulai Hu
In the presence of pinacolone, the in situ prepared triorganoaluminium reagents reacted with aromatic aldehydes to give ketones in moderate to high yield. We propose that the products are formed via a tandem organoaluminium reagents addition-Oppenauer oxidation sequence.

History

Related Materials

  1. 1.
    DOI - Is published in 10.1039/c3ob40642c
  2. 2.
    ISSN - Is published in 14770520

Journal

Organic and Biomolecular Chemistry

Volume

11

Issue

27

Start page

4429

End page

4432

Total pages

4

Publisher

R S C Publications

Place published

United Kingdom

Language

English

Copyright

© The Royal Society of Chemistry 2013

Former Identifier

2006045735

Esploro creation date

2020-06-22

Fedora creation date

2015-01-19

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