Unusual Diastereofacial Selectivity in the Michael Addition Reactions of Lithiated 2-Aminoacetates and -acetamides to α,β-Unsaturated Carbonyl Compounds
- 1 September 1992
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 21 (9), 1801-1804
- https://doi.org/10.1246/cl.1992.1801
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Asymmetric Michael Addition of the N-Alkylidene Derivative of an α-Amino Ester to Methyl (E)-3-[(3R,7aS)-2-Phenylperhydropyrrolo[1,2-c]imidazol-3-yl]propenoateBulletin of the Chemical Society of Japan, 1991
- Highly diastereoselective Michael addition of lithiated camphor imines of glycine esters to .alpha.,.beta.-unsaturated esters. Synthesis of optically pure 5-oxo-2,4-pyrrolidinedicarboxylates of unnatural stereochemistryThe Journal of Organic Chemistry, 1991
- A computational study of the 1,4-addition of lithium enolates to conjugated carbonyl compounds.Tetrahedron Letters, 1991
- Silicon directed diastereo- and enantioselective mukaiyama michael tandem aldol condensation: a novel strategy for six membered ring cyclisationTetrahedron Letters, 1990
- Stereoselective Michael addition of the imines of .alpha.-amino esters in the presence of lithium bromide/1,8-diazabicyclo[5.4.0]undec-7-eneThe Journal of Organic Chemistry, 1990
- Acyclic stereoselection. 46. Stereochemistry of the Michael addition of N,N-disubstituted amide and thioamide enolates to .alpha.,.beta.-unsaturated ketonesThe Journal of Organic Chemistry, 1990
- Stéréospécificité de l'addition de Michael d'ènethiolates avec les énones acycliquesTetrahedron, 1989
- Diastereoselective and enantioselective total synthesis of the hepatoprotective agent clausenamideThe Journal of Organic Chemistry, 1987
- A diastereo- and enantioselective Michael addition of chiral amide enolates to α, β-unsaturated esters a stereoelective synthesis of (+)-dehydroiridodiol and (−)-isodehydroiridodiolTetrahedron Letters, 1986
- Acyclic stereoselection. 31. Stereoselection in the Michael addition reaction. 3. Relationship between ester enolate geometry and adduct stereochemistry in the kinetic Michael reaction of lithium enolates with enonesThe Journal of Organic Chemistry, 1985