Stereoselective synthesis of enantiopure amino compounds, via Mitsunobu azidation of (2S,R-S)-1-(p-tolylsulfinyl)butan-2-ol

Citation
P. Bravo et al., Stereoselective synthesis of enantiopure amino compounds, via Mitsunobu azidation of (2S,R-S)-1-(p-tolylsulfinyl)butan-2-ol, J CHEM R-S, (10), 1998, pp. 666-667
Citations number
13
Categorie Soggetti
Chemistry
Journal title
JOURNAL OF CHEMICAL RESEARCH-S
ISSN journal
03082342 → ACNP
Issue
10
Year of publication
1998
Pages
666 - 667
Database
ISI
SICI code
0308-2342(199810):10<666:SSOEAC>2.0.ZU;2-M
Abstract
Azidation of (2S,R-S)-1-(p-tolysulfinyl)butan-2-ol under Mitsunobu conditio ns is the key step for a highly stereoselective preparation of enantiomeric ally pure amino compounds via chiral sulfoxide chemistry.