Scalable Synthesis of Esp and Rhodium(II) Carboxylates from Acetylacetone and RhCl·HO.

Org Process Res Dev

Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, 106 91 Stockholm, Sweden.

Published: June 2020

Rhodium(II) carboxylates are privileged catalysts for the most challenging carbene-, nitrene-, and oxo-transfer reactions. In this work, we address the strategic challenges of current organic and inorganic synthesis methods to access these rhodium(II) complexes through an oxidative rearrangement strategy and a reductive ligation reaction. These studies illustrate the multiple benefits of oxidative rearrangement in the process-scale synthesis of congested carboxylates over nitrile anion alkylation reactions, and the impressive effect of inorganic additives in the reductive ligation of rhodium(III) salts.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7309316PMC
http://dx.doi.org/10.1021/acs.oprd.0c00164DOI Listing

Publication Analysis

Top Keywords

rhodiumii carboxylates
8
oxidative rearrangement
8
reductive ligation
8
scalable synthesis
4
synthesis esp
4
esp rhodiumii
4
carboxylates acetylacetone
4
acetylacetone rhcl·ho
4
rhcl·ho rhodiumii
4
carboxylates privileged
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!