meso Epoxides in Asymmetric Synthesis: Enantioselective Opening by Nucleophiles in the Presence of Chiral Lewis Acids
- 1 September 1992
- journal article
- highlight
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 31 (9) , 1179-1180
- https://doi.org/10.1002/anie.199211791
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Catalytic Enantioselective Epoxidations of Simple OlefinsAngewandte Chemie International Edition in English, 1991
- Katalytische enantioselektive Epoxidierungen einfacher OlefineAngewandte Chemie, 1991
- Asymmetric Ring Opening of Symmetrical Epoxides with Trimethylsilyl Azide Using Chiral Titanium ComplexesSynlett, 1991
- Neue chirale Tripod‐Phosphane mit C3‐SymmetrieAngewandte Chemie, 1990
- New Chiral C3‐Symmetric Tripodal PhosphanesAngewandte Chemie International Edition in English, 1990
- Synthese und Struktur eines chiralen,C3-symmetrischen MonophosphansAngewandte Chemie, 1988
- Synthesis and Crystal Structure of a ChiralC3-Symmetric MonophosphaneAngewandte Chemie International Edition in English, 1988
- Metal(II) d-Tartrates Catalyzed Asymmetric Ring Opening of Oxiranes with Various NucleophilesBulletin of the Chemical Society of Japan, 1988
- A New Synthesis of Optically Active trans β-Amino Alcohols by Asymmetric Ring-opening of Symmetrical OxiranesChemistry Letters, 1987
- Asymmetric induction. 3. Enantioselective deprotonation by chiral lithium amide basesThe Journal of Organic Chemistry, 1980