Highly Enantioselective Alkylation of Tetrahydroisoquinolines via a Valine Chiral Auxiliary; Asymmetric Synthesis of (S)-Isoquinoline Alkaloids
- 1 June 1984
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 23 (6) , 458-459
- https://doi.org/10.1002/anie.198404581
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Enantioselective alkylation ofα-amino carbanionsTetrahedron, 1984
- Chromatographic separation of the enantiomers of acylated amines on chiral stationary phasesThe Journal of Organic Chemistry, 1984
- Alkylation of the isoquinoline skeleton in the 1-positionTetrahedron, 1983
- Asymmetric alkylation of α-amino carbanions. An enantioselective synthesis of (S)-1-alkyl-1,2,3,4-tetrahydroisoquinolinesJournal of the American Chemical Society, 1983
- The Constituents of Dysoxylum lenticellare. I. Phenylethylisoquinoline, Homoerythrina, and Dibenzazecine AlkaloidsJournal of Natural Products, 1983
- Induktion von Asymmetrie durch AminosäurenAngewandte Chemie, 1982
- Induction of Asymmetry by Amino AcidsAngewandte Chemie International Edition in English, 1982
- Dipole stabilized α-amino carbanions. II. Alkylation of tetrahydroisoquinolines in the 1-position.Tetrahedron Letters, 1981
- Absolute stereochemistry of securinineTetrahedron, 1963