Diastereoselective Addition of Organometallics to Chiral α-Keto Amides Having trans-2,5-Disubstituted Pyrrolidine
- 1 September 1990
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 19 (9) , 1749-1752
- https://doi.org/10.1246/cl.1990.1749
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- The First Direct Evidence for a Cram ChelateAngewandte Chemie International Edition in English, 1987
- Asymmetric synthesis of functionalized tertiary homoallyl alcohols by diastereoselective allylation of chiral .alpha.-keto amides derived from (S)-proline esters: control of stereochemistry based on saturated coordination of Lewis acidThe Journal of Organic Chemistry, 1986
- CH3Li/TiCl4: A non-basic and highly selective grignard analogueTetrahedron, 1986
- Asymmetric dialkylation of α-cyanoacetic acidTetrahedron Letters, 1986
- Concerning the role of Lewis acids in chelation controlled addition to chiral alkoxy aldehydesTetrahedron Letters, 1984
- Chelation or Non‐Chelation Control in Addition Reactions of Chiral α‐ and β‐ Alkoxy Carbonyl Compounds [New Synthetic Methods (44)]Angewandte Chemie International Edition in English, 1984
- 1,3-Asymmetric induction in addition reactions of chiral .beta.-alkoxy aldehydes: efficient chelation control via Lewis acidic titanium reagentsJournal of the American Chemical Society, 1983
- Stereoselective reduction of α-hydroxy ketonesTetrahedron Letters, 1983
- Highly stereocontrolled reduction of α′-alkoxyenones to give either the threo or eryhtro allylic 1,2-diol. Assignment of the threo configuration to the C-15, C-16 diol of pumiliotoxin B.1Tetrahedron Letters, 1982