Synthesis of the C1′–C11′ portion of pamamycin-607 via a stereoselective oxymercuration of a gamma—silyloxyallene and a stereospecific magnesium—methanol reduction
- 1 January 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (43) , 5505-5508
- https://doi.org/10.1016/s0040-4039(00)80798-4
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Directed reduction of .beta.-hydroxy ketones employing tetramethylammonium triacetoxyborohydrideJournal of the American Chemical Society, 1988
- Selective reduction of α,β-unsaturated esters in the presence of olefinsTetrahedron Letters, 1987
- Stereoselectivity in the syntheses of substituted 2-(2-tetrahydrofuranyl)acrylates via intramolecular oxymercurations or oxypalladations of allenesTetrahedron Letters, 1987
- Structure of pamamycin-607, an aerial mycelium-inducing substance of Streptomyces albonigerTetrahedron 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
- Enantiodivergent syntheses of (+)- and (-)-nonactic acid and the total synthesis of nonactinJournal of the American Chemical Society, 1984
- Pamamycin: A new antibiotic and stimulator of aerial mycelia formation.The Journal of Antibiotics, 1979