TRANSITION-METAL-CATALYZED OXIDATION .8. 4-ALLYL-SUBSTITUTED 1,2-NAPHTHOQUINONES VIA TANDEM ORTHO-PHENOL OXYGENATION AND OXY-COPE REARRANGEMENT

Citation
K. Krohn et S. Bernhard, TRANSITION-METAL-CATALYZED OXIDATION .8. 4-ALLYL-SUBSTITUTED 1,2-NAPHTHOQUINONES VIA TANDEM ORTHO-PHENOL OXYGENATION AND OXY-COPE REARRANGEMENT, Synthesis, (6), 1996, pp. 699
Citations number
13
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00397881
Issue
6
Year of publication
1996
Database
ISI
SICI code
0039-7881(1996):6<699:TO.41>2.0.ZU;2-S
Abstract
4-Allyl-1,2-naphthoquinones 3a-3d are prepared in one operation from 2 -allyl-1-naphthols 2a-2d involving tandem zirconium-catalyzed tert-but yl hydroperoxide (TBHP) oxidation and oxy-Cope rearrangement.