References
- Stecher , P. G. 1968 . The Merck Index , 1049 New. Jersey : Merck & Co. Inc. .
- Gripenberg , J. 1951 . Acta Chem. Scandinavica , 5 : 995 and other references cited therein
- Quon , H. H. and Swan , E. P. 1969 . Canad. J. Chem. , 47 : 4389
- Stork , G. , Meisels , A. and Davies , J. E. 1963 . J. Amer. Chem. Soc. , 85 : 3419
- Fujimoto , Y. and Ikekawa , N. 1976 . Chem. Pharm. Bull. , 24 : 825
- Martin , E. L. 1942 . Org. Reactions , 1 : 155
- Brown , H. C. , Knights , E. F. and Seouten , C. G. 1974 . J. Amer. Chem. Soc. , 96 : 7765
- Bhaca , N. S. and Williams , D. H. 1969 . Application of NMR Spectroscopy in Organic Chemistry , 69 San Francisco : Holden-Day, Inc. .
- Ireland , R. E. and Mander , L. N. 1969 . J. Org. Chem. , 34 : 142 There is ample evidence that low-temperature Jones oxidation of alcohols to enolizable ketones proceeds without epimerization of an asymetric center α to the ketone function, see
- Stork , G. and Burgstahler , A. 1951 . J. Amer. Chem. Soc. , 73 : 3544 An alternative approach for the synthesis of ketone 9 has been reported, see
- Olefin 17 was found to be extremely unstable to light whose colour changed rapidly from faint yellow to deep red. Thus it was immediately used for the next step
- Grant , P. K. , Huntrakul , G. and Shepard , D. R. J. 1967 . Aus. J. Chem. , 20 : 969