Generation of a configurationally stable, enantioenriched α-oxy-α-methylbenzyllithium: Stereodivergence of its electrophilic substitution
- 1 January 1994
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 50 (20) , 6097-6108
- https://doi.org/10.1016/s0040-4020(01)90461-2
Abstract
No abstract availableThis publication has 58 references indexed in Scilit:
- Stereochemical studies on chiral, nonconjugated, nitrogen-substituted carbanions generated by tin-lithium exchangeJournal of the American Chemical Society, 1991
- η1‐(1S, 2E)‐1‐(N,N‐diisopropylcarbamoyloxy)‐3‐trimethylsilylallyllithium(-)‐Sparteine: Structure of a Chiral, Carbamoyloxy‐substituted Allyllithium CompoundAngewandte Chemie International Edition in English, 1991
- Generation of a Configurationally Stable Chiral Benzyllithium Derivative, and the Capricious Stereochemistry of Its Electrophilic SubstitutionAngewandte Chemie International Edition in English, 1990
- Chiral Lithium‐1‐oxyalkanides by Asymmetric Deprotonation; Enantioselective Synthesis of 2‐Hydroxyalkanoic Acids and Secondary AlkanolsAngewandte Chemie International Edition in English, 1990
- Superbases for organic synthesisPublished by Walter de Gruyter GmbH ,1988
- A convenient method for estimation of alkyllithium concentrationsThe Journal of Organic Chemistry, 1976
- Electrophilic Substitution at Saturated Carbon. XIV. Asymmetric Solvation of Carbanions in Stereospecific Hydrogen-Deuterium Exchange Reactions1,2Journal of the American Chemical Society, 1961
- Electrophilic Substitution at Saturated Carbon. VI. Stereochemical Capabilities of Carbanions1Journal of the American Chemical Society, 1959
- Studies in Stereochemistry. XXX. Models for Steric Control of Asymmetric Induction1Journal of the American Chemical Society, 1959
- Studies in Stereochemistry. XXIII. The Preparation and Complete Resolution of the 1,2-Diphenyl-2-methyl-1-butanol System1Journal of the American Chemical Society, 1954