Asymmetric synthesis via acetal templates. 15. The preparation of enantiomerically pure mevinolin analogs
Open Access
- 1 January 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (31) , 3757-3760
- https://doi.org/10.1016/s0040-4039(00)82107-3
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Synthesis of an HMG-CoA reductase inhibitor; a diastereoselective aldol approachTetrahedron Letters, 1987
- 1,3- diastereoselective reduction of β-hydroxyketones utilizing alkoxydialkylboranesTetrahedron Letters, 1987
- Asymmetric synthesis via acetal templates. 13. Preparation of aldol compounds from butane-1,3-diol acetalsThe Journal of Organic Chemistry, 1987
- 3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 3. 7-(3,5-Disubstituted-[1,1'-biphenyl]-2-yl)-3,5-dihydroxy-6-heptenoic acids and their lactone derivativesJournal of Medicinal Chemistry, 1986
- A diastereospecific, non-racemic synthesis of a novel β-hydroxy-δ-lactone HMG-CoA reductase inhibitorTetrahedron Letters, 1985
- Synthetic and biological studies of compactin and related compounds. 2. Synthesis of the lactone moiety of compactinThe Journal of Organic Chemistry, 1984
- Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketonesThe Journal of Organic Chemistry, 1983
- Chemistry of enol silyl ethers. A general synthesis of 3-hydroxyhomophthalates and a biomimetic synthesis of sclerinCanadian Journal of Chemistry, 1983
- Über die Depolymerisierung von Poly‐(R)‐3‐hydroxy‐buttersäureester (PHB)Helvetica Chimica Acta, 1982
- Monacolin K, a new hypocholesterolemic agent produced by a Monascus species.The Journal of Antibiotics, 1979