THE CHIRAL AMINO ALCOHOL, CIS-2-AMINO-1-ACENAPHTHENOL - SYNTHESIS, RESOLUTION, AND APPLICATION TO THE DIASTEREOSELECTIVE [2,3]-WITTIG REARRANGEMENT

Authors
SUDO A HASHIMOTO Y KIMOTO H HAYASHI K SAIGO K
Citation
A. Sudo et al., THE CHIRAL AMINO ALCOHOL, CIS-2-AMINO-1-ACENAPHTHENOL - SYNTHESIS, RESOLUTION, AND APPLICATION TO THE DIASTEREOSELECTIVE [2,3]-WITTIG REARRANGEMENT, Tetrahedron : asymmetry, 5(7), 1994, pp. 1333-1346
Citations number
29
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
5
Issue
7
Year of publication
1994
Pages
1333 - 1346
Database
ISI
SICI code
0957-4166(1994)5:7<1333:TCAAC->2.0.ZU;2-D
Abstract
The chiral amino alcohol, cis-2-amino-1-acenaphthenol, was synthesized , and resolved by a simple procedure. This new chiral amino alcohol wa s converted into an oxazoline derivative and applied as a chiral auxil iary to the diastereoselective [2,3]-Wittig rearrangement.