A stereoselective concise synthesis of C2- and meso-aminodiols from (R)-phenylglycinol
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Stereoselective reduction of prochiral ketones, using aluminum hydride reagents prepared from lialh4 and chiral diethanolamines.
2. A chiral samarium-based catalyst for the asymmetric Meerwein-Ponndorf-Verley reduction
3. A modular approach for ligand design for asymmetric allylic alkylations via enantioselective palladium-catalyzed ionizations
4. Transimination. Conversion of nitriles into secondary amines in a one-pot reaction
5. Synthesis of chiral diaza-18-crown-6 derivatives from optically active diethanolamines
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1. Homoallylic amines as efficient chiral inducing frameworks in the conjugate addition of amides to α,β-unsaturated esters. An entry to enantio-enriched diversely substituted amines;Organic & Biomolecular Chemistry;2020
2. Asymmetric Synthesis of Both Diastereomers of α,α′-disubstituted Iminodiacetic Acid Derivatives Using Stereoselective Nucleophilic Substitution of α-Bromo Esters;Bulletin of the Korean Chemical Society;2018-04-06
3. Formation of Amines from Other Amines and Derivatives;Comprehensive Organic Transformations;2018-02-28
4. ChemInform Abstract: A Stereoselective Concise Synthesis of C2- and meso-Aminodiols from (R) -Phenylglycinol.;ChemInform;2010-08-18
5. Concise Synthesis of Tricyclic Isoindolinones via One-Pot Cascade Multicomponent Sequences;Organic Letters;2009-03-25
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