A highly stereoselective conversion of α,β-epoxy esters to α-hydroxy esters. An efficient route to optically active α-hydroxyesters
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (38) , 4435-4436
- https://doi.org/10.1016/s0040-4039(00)96531-6
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
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- Nucleophilic opening of 2,3-epoxy acids and amides mediated by titanium isopropoxide. Highly enhanced C-3 selectivityThe Journal of Organic Chemistry, 1985
- Regioselective openings of 2,3-epoxy acids with organocupratesTetrahedron Letters, 1985
- A Convenient Synthesis of α-Keto-esters and Unsymmetrical 1,2-Diketones from Carbonyl CompoundsSynthesis, 1975