Synthesis and application of C-2-symmetric diamino FERRIPHOS as ligands for enantioselective Rh-catalyzed preparation of chiral alpha-amino acids

Citation
Jja. Perea et al., Synthesis and application of C-2-symmetric diamino FERRIPHOS as ligands for enantioselective Rh-catalyzed preparation of chiral alpha-amino acids, TETRAHEDR-A, 10(2), 1999, pp. 375-384
Citations number
36
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON-ASYMMETRY
ISSN journal
09574166 → ACNP
Volume
10
Issue
2
Year of publication
1999
Pages
375 - 384
Database
ISI
SICI code
0957-4166(19990129)10:2<375:SAAOCD>2.0.ZU;2-O
Abstract
C-2-Symmetrical ferrocenyl diamino diphosphines (diamino FERRIPHOS ligands) proved to be excellent ligands for the rhodium-catalyzed enantioselective reduction of methyl alpha-acetamidoacrylates, The straightforward synthesis , their air stability and the easy modification of their structure makes th ese ligands especially interesting for transition metal-catalyzed hydrogena tions. alpha-Amino acids with enantioselectivities greater than 95% (and up to 99.3% ee) were obtained with no need of further recrystallization. (C) 1999 Elsevier Science Ltd. All rights reserved.