New strategies for the construction of macrolide antibiotic subunits using organoiron precursors
- 1 January 1985
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 41 (24) , 5765-5770
- https://doi.org/10.1016/s0040-4020(01)91415-2
Abstract
No abstract availableThis publication has 28 references indexed in Scilit:
- Organoiron complexes in organic synthesis. 33. Tricarbonylcyclohexadienyliron complexes as aryl cation equivalents: a formal synthesis of (.+-.)-O-methyljoubertiamineThe Journal of Organic Chemistry, 1984
- Iron-Stabilized Carbocations as Intermediates for Organic SynthesisScience, 1984
- Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistryJournal of the American Chemical Society, 1983
- Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenonesThe Journal of Organic Chemistry, 1982
- Diene and dienyl complexes of iron: Reactivity and synthetic utilityTransition Metal Chemistry, 1981
- Tricarbonyl(diene)iron complexes: synthetically useful propertiesAccounts of Chemical Research, 1980
- Cyclofunctionalization of olefinic urethanes using benzeneselenenyl chloride in the presence of silica gel: a general route to nitrogen heterocyclesThe Journal of Organic Chemistry, 1980
- Phenylseleno- and phenylsulfenolactonizations. Two highly efficient and synthetically useful cyclization proceduresJournal of the American Chemical Society, 1979
- Nachbargruppenbeteiligung bei Additionsreaktionen, IV. Darstellung von α.α‐disubstituierten δ‐Arylselenenyl‐und δ‐Aryltelluro‐γ‐valerolactonenEuropean Journal of Inorganic Chemistry, 1960
- Addition of tellurium compounds to double bondsTetrahedron Letters, 1959