A facile entry to β,δ-diketo and syn-β,δ-dihydroxy esters
- 1 January 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (49) , 6467-6470
- https://doi.org/10.1016/s0040-4039(00)82375-8
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Synthesis of a novel HMG-COA reductase inhibitorTetrahedron Letters, 1988
- Asymmetric synthesis via acetal templates. 15. The preparation of enantiomerically pure mevinolin analogsTetrahedron Letters, 1988
- A Novel Method for the In situ Generation of Alkoxydialkylboranes and Their Use in the Selective Preparation of 1,3-syn DiolsChemistry Letters, 1987
- Total synthesis and biological evaluation of structural analogs of compactin and dihydromevinolinJournal of Medicinal Chemistry, 1987
- 1,3- diastereoselective reduction of β-hydroxyketones utilizing alkoxydialkylboranesTetrahedron Letters, 1987
- Synthesis of an HMG-CoA reductase inhibitor; a diastereoselective aldol approachTetrahedron Letters, 1987
- 1,3-syn diastereoselective reduction of β-hydroxyketones with diisobutylaluminum hydride and tributyltin hydrideTetrahedron Letters, 1986
- Stereoselective Reduction of δ‐Hydroxy‐β‐ketoestersHelvetica Chimica Acta, 1986
- Compactin (ML-236B) and related compounds as potential cholesterol-lowering agents that inhibit HMG-CoA reductaseJournal of Medicinal Chemistry, 1985
- Stereoselective reduction of β hydroxyketones to 1,3-diols highly selective 1,3-asymmetric induction via boron chelatesTetrahedron, 1984