ENANTIOSELECTIVE SYNTHESIS OF N-FMOC PROTECTED DI-TERT-BUTYL 4-PHOSPHONOMETHYL-L-PHENYLALANINE - A HYDROLYTICALLY STABLE ANALOG OF O-PHOSPHOTYROSINE

Authors
LIU WQ ROQUES BP GARBAYJAUREGUIBERRY C
Citation
Wq. Liu et al., ENANTIOSELECTIVE SYNTHESIS OF N-FMOC PROTECTED DI-TERT-BUTYL 4-PHOSPHONOMETHYL-L-PHENYLALANINE - A HYDROLYTICALLY STABLE ANALOG OF O-PHOSPHOTYROSINE, Tetrahedron : asymmetry, 6(3), 1995, pp. 647-650
Citations number
18
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
6
Issue
3
Year of publication
1995
Pages
647 - 650
Database
ISI
SICI code
0957-4166(1995)6:3<647:ESONPD>2.0.ZU;2-5
Abstract
Fmoc-L-Pmp(tBu)(2)-OH was prepared with high enantiomeric purity by an asymmetric synthetic pathway, using a camphor sultam as chiral auxili ary.