Asymmetric Radical Addition of TEMPO to Titanium Enolates
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of California, Santa Barbara, California 93106-9510, United States
Funder
NSF Office of the Director
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol403398u
Reference30 articles.
1. General and Efficient α-Oxygenation of Carbonyl Compounds by TEMPO Induced by Single-Electron-Transfer Oxidation of Their Enolates
2. Transition-metal peroxide reactions. Synthesis of .alpha.-hydroxycarbonyl compounds from enolates
3. HYDROXYLATION OF ENOLATES WITH OXODIPEROXYMOLYBDENUM(PYRIDINE)(HEXAMETHYLPHOSPHORIC TRIAMIDE), MoO5·Py·HMPA(MoOPH): 3-HYDROXY-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPTAN-2-ONE
4. Org. Synth. Coll. Vol. 7 1990, 277–282.
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