BUTOXYCARBONYL-2-(TERT-BUTYLDIMETHYLSILOXY)PYRROLE AS A GLYCINE ANIONEQUIVALENT - A FLEXIBLE ENANTIOSELECTIVE ACCESS TO POLYHYDROXY-ALPHA-AMINO ACIDS

Authors
CASIRAGHI G RASSU G SPANU P PINNA L
Citation
G. Casiraghi et al., BUTOXYCARBONYL-2-(TERT-BUTYLDIMETHYLSILOXY)PYRROLE AS A GLYCINE ANIONEQUIVALENT - A FLEXIBLE ENANTIOSELECTIVE ACCESS TO POLYHYDROXY-ALPHA-AMINO ACIDS, Tetrahedron letters, 35(15), 1994, pp. 2423-2426
Citations number
22
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
35
Issue
15
Year of publication
1994
Pages
2423 - 2426
Database
ISI
SICI code
0040-4039(1994)35:15<2423:BAAGA>2.0.ZU;2-Q
Abstract
An efficient stereoselective route to polyhydroxy-alpha-amino acids 7a -f was developed by exploiting butoxycarbonyl-2-(tert-butyldimethylsil oxy)pyrrole as a glycine anion equivalent.