Cu‐Catalyzed Tandem Oxidation‐Intramolecular Cannizzaro Reaction of Biorenewables and Bioactive Molecules

Author:

Petkov Hristo1,Ravutsov Martin A.1,Verganista Manuel J.2,Mitrev Yavor N.1,Candeias Nuno R.23,Simeonov Svilen P.14ORCID

Affiliation:

1. Institute of Organic Chemistry with Centre of Phytochemistry Bulgarian Academy of Sciences Acad. G. Bonchev str., bl. 9 Sofia 1113 Bulgaria

2. LAQV-REQUIMTE Department of Chemistry University of Aveiro 3810-193 Aveiro Portugal

3. Faculty of Engineering and Natural Sciences Tampere University Korkeakoulunkatu 8 33101 Tampere Finland

4. Research Institute for Medicines (iMed.ULisboa) Faculty of Pharmacy Universidade de Lisboa Av. Prof. Gama Pinto 1649-003 Lisbon Portugal

Abstract

AbstractA tandem Cu‐catalyzed oxidation‐intramolecular Cannizzaro reaction leading to bioactive α‐hydroxyesters from α‐hydroxyketones is reported. The process uses oxygen as a sole oxidant to achieve the formation of glyoxals, which are efficiently converted in situ to important α‐hydroxyesters. The mechanistic insights are provided by isotopic labeling and supported by DFT calculations. The transformation proved a robust synthetic tool to achieve the synthesis of human metabolites and hydroxyl esters of various biologically active steroid derivatives.

Publisher

Wiley

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Synthetic applications of the Cannizzaro reaction;Beilstein Journal of Organic Chemistry;2024-06-19

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