Switching Enantiofacial Selectivities Using One Chiral Source: Catalytic Enantioselective Synthesis of the Key Intermediate for (20S)-Camptothecin Family by (S)-Selective Cyanosilylation of Ketones
- 14 September 2001
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 123 (40) , 9908-9909
- https://doi.org/10.1021/ja016682n
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Catalytic enantioselective cyanosilylation of ketones: improvement of enantioselectivity and catalyst turn-over by ligand tuningTetrahedron Letters, 2001
- Catalytic Enantioselective Cyanosilylation of KetonesJournal of the American Chemical Society, 2000
- The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon StereocentersAngewandte Chemie International Edition in English, 1998
- A General Synthetic Approach to the (20S)-Camptothecin Family of Antitumor Agents by a Regiocontrolled Cascade Radical Cyclization of Aryl IsonitrilesChemistry – A European Journal, 1998