2,6-Bis[(2S)-tetrahydrofuran-2-yl]phenyl diselenide: An effective reagent for asymmetric electrophilic addition reactions to olefins
- 1 July 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (27) , 4753-4756
- https://doi.org/10.1016/s0040-4039(97)01030-7
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Design of optically active selenium reagents having a chiral tertiary amino group and their application to asymmetric inter- and intramolecular oxyselenenylationsTetrahedron, 1997
- Palladium(II)-catalyzed formation of γ-butyrolactones from 4-trimethylsilyl-3-alkyn-1-ols: Synthetic and mechanistic aspectsTetrahedron, 1996
- Practical Synthesis of (R,R)- and (S,S)-Bis[2,6-bis(1-ethoxyethyl)phenyl] DiselenideThe Journal of Organic Chemistry, 1996
- Asymmetric cyclization of unsaturated alcohols and carboxylic acids with camphor-based selenium electrophilesChemical Communications, 1996
- Asymmetric Reaction of Arylalkenes with DiselenidesAngewandte Chemie International Edition in English, 1995
- Asymmetric Ring Closure Reactions Mediated by a Chiral C2 Symmetrical Organoselenium ReagentThe Journal of Organic Chemistry, 1995
- Highly selective asymmetric intramolecular selenocyclisationJournal of the Chemical Society, Chemical Communications, 1995
- Asymmetric selenomethoxylation of olefins involving a chiral C2 symmetrical electrophilic organoselenium reagentThe Journal of Organic Chemistry, 1993
- Tandem michael-michael-ring closure (mimirc) reactionsTetrahedron, 1981
- Organic tellurium and selenium chemistry. Reduction of tellurides, selenides, and selenoacetals with triphenyltin hydrideJournal of the American Chemical Society, 1980