3-Methyl-γ-butyrolactone as a source of 2-methyl-3-hydroxyketones and 2-methyl-1,3-diols: a synthesis of the C19C27 fragment of rifamycin S by linear iteration
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (16) , 1725-1728
- https://doi.org/10.1016/s0040-4039(00)95405-4
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- Total synthesis of elaiophylin (azalomycin B)Tetrahedron Letters, 1986
- Regiochemical control in the hemiacetalization of a dihydroxydialdehyde. An application of the use of homochiral 3-methyl-δ-butyrolactones to the construction of homochiral tripropionate units.Tetrahedron Letters, 1986
- Total synthesis of (+)-11,11'-di-O-methylelaiophylidene, an aglycon of elaiophylinJournal of the American Chemical Society, 1985
- Tetrahedron report number 190Tetrahedron, 1985
- An introduction of chiral centers into acyclic systems based on stereoselective ketone reductionAccounts of Chemical Research, 1984
- Stereoselective reduction of β hydroxyketones to 1,3-diols highly selective 1,3-asymmetric induction via boron chelatesTetrahedron, 1984
- Stereocontrolled total synthesis of Antibiotic A-23187 (calcimycin)Journal of the American Chemical Society, 1982
- Stoffwechselprodukte von Mikroorganismen. 211. Milteilung. Röntgenstrukturanalyse von ElaiophylinHelvetica Chimica Acta, 1982
- Total synthesis of rifamycins. 1. Stereocontrolled synthesis of the aliphatic building blockJournal of the American Chemical Society, 1980
- Structure of A23187, a divalent cation ionophoreJournal of the American Chemical Society, 1974