Enantioselective aldol reaction mediated by chiral lithium amide bases
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Stereoselective Aldol Reactions withα-Unsubstituted Chiral Enolates
2. ENANTIOSELECTIVE CROSS ALDOL REACTION VIA DIVALENT TIN ENOLATE
3. Enantioselektive 1,2-Additionen von Li-, Mg-, Zn- und Cu-organischen Verbindungen und von Li-Enolaten an Carbonylverbindungen im chiralen Medium DDB
4. Stereoselective additions to carboxylic acid dianions and β-lactone substituted ester enolates
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1. Enantioselective [2,3]-Wittig Rearrangement of Carboxylic Acid Derived Enolates by Tetradentate Chiral Lithium Amide;Synlett;2023-02-21
2. Formation of Aldehydes and Ketones by Condensation Reactions;Comprehensive Organic Transformations;2018-02-28
3. An Effect of H-bonding in Synthesis of 1, 5-Diketones via Tandem Aldol-Michael Addition Reaction Using Room Temperature Ionic Liquid (RTIL).;ChemistrySelect;2017-02-13
4. Nucleophilic Species That Form Carbon-Carbon Bonds;Organic Synthesis;2017
5. Chiral Lithium Amides: Tuning Asymmetric Synthesis on the Basis of Structural Parameters;The Chemical Record;2016-12-20
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