1,2-Asymmetric induction in the radical addition of organotin hydrides to (−)-menthyl(E)-2,3-disubstituted propenoates
- 30 March 1998
- journal article
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 555 (2) , 151-159
- https://doi.org/10.1016/s0022-328x(97)00637-2
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Acyclic Diastereofacial Selection in Intermolecular Radical Reactions StericvsElectronic ControlsSynlett, 1994
- Stereoselective hydrostannation: Synthesis and absolute configuration of (−)-menthyl 2,3-diphenyl-3-(trimethylstannyl) propanoates and derivativesJournal of Organometallic Chemistry, 1992
- Acyclic stereochemical control in free-radical reactionsAccounts of Chemical Research, 1991
- Experimental test of karplus‐type relationships for 3J(Sn, C) and 3J(Sn, H)Magnetic Resonance in Chemistry, 1988
- Organotin compounds. 6. Hydrostannation of methyl (E)-disubstituted propenoates with trimethyltin hydride and dimethyltin chlorohydrideOrganometallics, 1985
- Organotin compoundsJournal of Organometallic Chemistry, 1982
- Organotin hydride additions to E- And Z-trisubstituted ethylenes synthesis of some new functionally substituted organotin compoundsJournal of Organometallic Chemistry, 1981
- Carbon-13 Fourier transform NMR study of the organotin compounds. II. Karplus-type dependence of vicinal tin-119-carbon-13 couplingJournal of the American Chemical Society, 1974
- The absolute configuration of αα′-diphenylsuccinic acid. The (±)-and meso-αα′-diphenylsuccinic anhydridesJournal of the Chemical Society C: Organic, 1968
- The Stereochemical Course of the Raney Nickel-catalyzed Cleavage of 2-Arylethanols1,2Journal of the American Chemical Society, 1959