Acyclic stereoselection via cyclic hydroboration. Synthesis of the Prelog-Djerassi lactonic acid.
- 31 December 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (38) , 3725-3728
- https://doi.org/10.1016/s0040-4039(01)82004-9
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Total synthesis of 6-deoxyerythronolide BJournal of the American Chemical Society, 1981
- The synthesis of chiral subunits for macrolide synthesis: the Prelog-Djerassi lactone and derivativesThe Journal of Organic Chemistry, 1981
- Remote asymmetric induction. A stereoselective approach to acyclic diols via cyclic hydroborationJournal of the American Chemical Society, 1980
- Highly Stereoselective Aldol Condensation Using an Enantioselective Chiral EnolateAngewandte Chemie International Edition in English, 1980
- Synthesis of the polyether antibiotic monensin. 2. Preparation of intermediatesJournal of the American Chemical Society, 1980
- Macrolide antibiotics. 1. Total synthesis of the Prelog-Djerassi lactone and methynolideJournal of the American Chemical Society, 1979
- Dehydrohalogenation by complex base. Preferential loss of "poorer" halogen leaving groupsJournal of the American Chemical Society, 1979
- Ruthenium(II) catalyzed rearrangement of diallyl ethers. A synthesis of .gamma.,.delta.-unsaturated aldehydes and ketonesThe Journal of Organic Chemistry, 1977
- The Structure of the Antibiotic Methymycin1Journal of the American Chemical Society, 1956
- Stoffwechselprodukte von Actinomyceten. 5. Mitteilung. Über das Lacton der β‐Hydroxy‐α, α′, γ‐trimethyl‐pimelinsäure, ein Abbauprodukt von Narbomycin, Pikromycin und MethymycinHelvetica Chimica Acta, 1956