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Diastereoselective aldol condensation with 2-(β-ethoxycarbonyl)oxazolidine derived from norephedrine. A chiral masked synthon of ethyl formylacetate

✍ Scribed by María García-Valverde; Javier Nieto; Rafael Pedrosa; Martina Vicente

Book ID
104209249
Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
467 KB
Volume
55
Category
Article
ISSN
0040-4020

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ChemInform Abstract: Diastereoselective
ChemInform Abstract: Diastereoselective Aldol Condensation with 2-(β-Ethoxycarbonyl)oxazolidine Derived from Norephedrine. A Chiral Masked Synthon of Ethyl Formylacetate.
✍ Maria Garcia-Valverde; Javier Nieto; Rafael Pedrosa; Martina Vicente 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB

Diastereoselective Aldol Condensation with 2-(β-Ethoxycarbonyl)oxazolidine Derived from Norephedrine. A Chiral Masked Synthon of Ethyl Formylacetate. -The aldol condensation of the title synthon (I) with aromatic aldehydes allows the synthesis of β-hydroxy esters with moderate to high diastereoselec