Enantioselective Alkylations of γ-Oxo Esters
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397918708077302
Reference14 articles.
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2. Etude d'un modele d'induction asymetrique: Les oxazolidines α,β-insaturees issues de l'ephedrine
3. Addition diastereoselective sur une double liaison en α d'une oxazolidine chirale
4. Chiral 1,4-dihydropyridine equivalents: a new approach to the asymmetric synthesis of alkaloids. The enantiospecific synthesis of (+)- and (-)-coniine and dihydropinidine
5. Trimethylchlorosilane induced ring opening of 2-alkyloxazolidines to enamine derivatives
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1. Formation of Nitriles, Carboxylic Acids, and Derivatives by Alkylation, Acylation, and Substitution;Comprehensive Organic Transformations;2018-02-28
2. Stability Studies of Oxazolidine-Based Compounds Using 1H NMR Spectroscopy;Journal of Pharmaceutical Sciences;2010-08
3. Synthesis of γ-Amino Esters via Mn-Mediated Radical Addition to Chiral γ-Hydrazonoesters;Organic Letters;2009-02-06
4. The Use of N ‐Boc‐1,3‐Oxazolidines as Chiral Auxiliaries in Asymmetric Synthesis;European Journal of Organic Chemistry;2004-02
5. Diastereoselective aldol condensation with 2-(β-ethoxycarbonyl)oxazolidine derived from norephedrine. A chiral masked synthon of ethyl formylacetate;Tetrahedron;1999-02
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