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- [3] 1,5-Asymmetric induction of chirality: diastereoselective addition of organoaluminium reagents and allylstannanes into aldehyclie groups in the side-chain of pi-allyltricarbonyliron lactone complexes JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1997, (22): : 3327 - 3337
- [4] 1,5-Asymmetric induction of chirality: highly diastereoselective addition reactions of organoaluminium reagents into ketone groups in the side-chain of pi-allyltricarbonyliron lactone complexes JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1997, (22): : 3299 - 3313
- [7] SYNTHESIS OF BETA-LACTAMS FROM PI-ALLYLTRICARBONYLIRON (LACTONE) COMPLEXES JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1983, (12): : 2851 - 2856
- [8] 1,5-Asymmetric induction of chirality: highly diastereoselective synthesis of homoallylic tertiary alcohols by the Lewis acid-mediated addition of allylstannanes into ketones in the side-chain of pi-allyltricarbonyliron lactone complexes JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1997, (22): : 3315 - 3325
- [9] Synthesis of beta-dimorphecolic acid exploiting highly stereoselective reduction of a side-chain carbonyl group in a pi-allyltricarbonyliron lactone complex JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1997, (08): : 1125 - 1133