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Chiral Diphosphites Derived from D ‐Glucose: New Ligands for the Asymmetric Catalytic Hydroformylation of Vinyl Arenes
Author(s) -
Diéguez Montserrat,
Pàmies Oscar,
Ruiz Aurora,
Castillón Sergio,
Claver Carmen
Publication year - 2001
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/1521-3765(20010716)7:14<3086::aid-chem3086>3.0.co;2-o
Subject(s) - stereocenter , hydroformylation , chemistry , ligand (biochemistry) , substituent , catalysis , rhodium , stereochemistry , enantioselective synthesis , asymmetric hydrogenation , biphenyl , medicinal chemistry , organic chemistry , receptor , biochemistry
A series of novel diphosphite ligands derived from readily available D ‐(+)‐glucose has been synthesized. These ligands have been applied to the Rh‐catalyzed hydroformylation of vinyl arenes. Both excellent enantioselectivities (up to 91 %) and regioselectivities (up to 98.8 %) were achieved under mild conditions. The advantage of these ligands is that their modular natures allow facile, systematic variation in the configurations at the stereocenters [C(3), C(5)] at the ligand bridge and in the biphenyl substituents, enabling their effects on the stereoselectivity to be studied. Results show that the absolute configuration of the product is governed by the configuration at the stereogenic center C(3), while the level of the enantioselectivity is influenced by a cooperative effect between stereocenters C(3) and C(5). Replacement of the tert ‐butyl substituent by methoxy substituents at the para positions of the biphenyl moieties improved the enantioselectivities. We have characterized the rhodium complexes formed under CO/H 2 by NMR techniques and in situ IR spectroscopy and have observed that there is a relationship between the structure of the [HRh(CO) 2 (PP)] species and their enantiodiscriminating performance in hydroformylation. Enantioselectivities were highest with ligands with a strong bis‐equatorial coordination preference, while an equilibrium of species with bis‐equatorial and equatorial‐axial coordination modes considerably reduced the ee 's.