Diastereoselective π-facially controlled nucleophilic additions of chiral vinylorganometallics to chiral β,γ-unsaturated ketones. 2. A practical method for stereocontrolled elaboration of the decahydro--indacene subunit of ikarugamycin
暂无分享,去创建一个
[1] L. Paquette,et al. Synthesis of a representative cis/trans pair of 4,5-disubstituted cyclopentenyllithium reagents , 1985 .
[2] M. J. O'brien,et al. Ikarugamycin: total synthesis of the decahydro-as-indacene portion , 1984 .
[3] R. K. Boeckman,et al. Stereocontrol in the intramolecular Diels-Alder reaction. 5. Preparation of a tetracyclic intermediate for ikarugamycin , 1983 .
[4] F. Tureček,et al. Structures of the tricyclododecenes prepared by the catalytical intramolecular cyclisation of 1,5,9-cyclododecatriene , 1979 .
[5] M. Nishizawa,et al. Remote double bond migration via rhodium catalysis: a novel enone transposition , 1976 .
[6] E. M. Burgess,et al. Thermal reactions of alkyl N-carbomethoxysulfamate esters , 1973 .
[7] Y. Kuroda,et al. A new antibiotic, ikarugamycin. , 1972, The Journal of antibiotics.