Diastereoselective fluorination of chiral imide enolates using n-fluoro-o-benzenedisulfonimide (nfobs)
- 25 February 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (9) , 1153-1156
- https://doi.org/10.1016/s0040-4039(00)91883-5
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- The enantioselective fluoroacetamide acetal claisen rearrangements of N-fluoroacetyl-trans-(2R,5R)-2,5-dimethylpyrrolidineTetrahedron Letters, 1991
- Synthesis of the monofluoro ketone peptide isostereThe Journal of Organic Chemistry, 1991
- N-fluoro-o-benzenedisulfonimide: a useful new fluorinating reagentTetrahedron Letters, 1991
- Preparation and properties of chiral fluoroorganic compoundsTetrahedron: Asymmetry, 1990
- The asymmetric synthesis of .alpha.-amino acids. Electrophilic azidation of chiral imide enolates, a practical approach to the synthesis of (R)- and (S)-.alpha.-azido carboxylic acidsJournal of the American Chemical Society, 1990
- ENANTIOMERICALLY PURE ETHYL (R)- AND (S)- 2-FLUOROHEXANOATE BY ENZYME-CATALYZED KINETIC RESOLUTIONOrganic Syntheses, 1990
- Enantioselective synthesis of monofluorinated chiral building blocks from malonic acidJournal of the Chemical Society, Perkin Transactions 1, 1990
- Tetrahedron report number 221Tetrahedron, 1987
- Asymmetric syntheses of α-amino acids from α-halogenated 10-sulfonamido-isobornyl esters.Tetrahedron Letters, 1986
- α-Fluorocarbonyl compounds and related chemistryTetrahedron, 1985