Use of the -vinyloxyborane derived from S-phenyl propanethioate for stereospecific aldol-type condensation. A simplified synthesis of the prelog-djerassi lactonic acid
- 31 December 1979
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 20 (41) , 3937-3940
- https://doi.org/10.1016/s0040-4039(01)86469-8
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Stereoselective synthesis of β-hydroxy-α-methylketones via - and -vinyloxyboranes generated directly from cyclohexyl ethyl ketoneTetrahedron Letters, 1979
- Stereoselective synthesis of β-hydroxy-α-methylcarboxylic acid thiol esters via vinyloxyboranesTetrahedron Letters, 1979
- Highly stereoselective synthesis of (.+-.)-.alpha.-multistriatinThe Journal of Organic Chemistry, 1979
- Dehydrohalogenation by complex base. Preferential loss of "poorer" halogen leaving groupsJournal of the American Chemical Society, 1979
- Acyclic stereoselection. 2. Synthesis of 3-hydroxy-2-methyl- and 3-hydroxy-2,4-dimethylcarboxylic acidsJournal of the American Chemical Society, 1977
- NEW CROSS-ALDOL REACTION Via VINYLOXYBORANESChemistry Letters, 1976
- Syntheses of macrolide antibiotics. I. MethymycinJournal of the American Chemical Society, 1975
- 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
- Studies in Stereochemistry. X. The Rule of “Steric Control of Asymmetric Induction” in the Syntheses of Acyclic SystemsJournal of the American Chemical Society, 1952