A Mild and Chemoselective Method for the Reduction of Conjugated Isoxazolines to β-Hydroxy Ketones
Author:
Affiliation:
1. Laboratorium für Organische Chemie, ETH-Zentrum, Universitätstrasse 16, CH-8092 Zürich, Switzerland.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol015885d
Reference14 articles.
1. (b) Torssell, K. B. G.Nitrile Oxides, Nitrones, and Nitronates in Organic Chemistry; VCH: Stuttgart, 1988.
2. Reduction of .DELTA.2-isoxazolines. 3. Raney nickel catalyzed formation of .beta.-hydroxy ketones
3. Selective carbon-carbon bond formation at the oxazole ring. Cycloadditions and Michael-type additions of ketenes to 1,3-oxazoles
4. Silyl nitronates in organic synthesis. Synthesis of 3(2H)-furanones
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