Novel P,N ligands derived from (R)- and (S)-1-phenylethylamine with (2R,5R)-2,5-dimethylphospholanyl groups (DuPHAMIN) for asymmetric catalysis

European Journal of Inorganic Chemistry

Volumn , Issue 9, 2003, Pages 1748-1755

  Brauer, David J ^a   Kottsieper, Konstantin W ^a   Roßenbach, Stefan ^a   Stelzer, Othmar ^a  

^a UNIVERSITY OF WUPPERTAL   (Germany)

Author keywords

Asymmetric catalysis; N,P ligands; Rhodium

Indexed keywords

CATALYSIS; CATALYST ACTIVITY; CHELATION; ENANTIOMERS; HYDROGENATION; LIGANDS; LITHIUM COMPOUNDS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; RHODIUM COMPOUNDS; SOLVENTS; SULFUR COMPOUNDS;

1-PHENYLETHYLAMINE; ASYMMETRIC CATALYSIS; CHELATING LIGANDS; DONOR ATOMS; ENANTIOMERIC PURITY; N,P LIGAND; P LIGANDS; P-N LIGANDS; RH COMPLEXES; STEREOGENIC CENTERS;

SALTS;

2,5 DIMETHYLPHOSPHOLANYL; 2,5 HEXANEDIOL; 2,5 NORBONADIENE; ALKANE DERIVATIVE; ALKENE DERIVATIVE; ALPHA METHYLBENZYLAMINE; ALUMINUM; CATION; CINNAMIC ACID DERIVATIVE; ESTER DERIVATIVE; HEXANE; LIGAND; LITHIUM DERIVATIVE; METHYL ACETAMIDOCINNAMATE; METHYL GROUP; PHOSPHORAMIDIC ACID; SULFATE; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC CATALYSIS; ATOMIC PARTICLE; CRYSTAL STRUCTURE; ENANTIOMER; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROGENATION; ISOMER; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; NUCLEAR OVERHAUSER EFFECT; PHOSPHORUS NUCLEAR MAGNETIC RESONANCE; PROTEIN TERTIARY STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; QUANTITATIVE ANALYSIS; REDUCTION; ROOM TEMPERATURE;

EID: 0038244977     PISSN: 14341948     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejic.200200388     Document Type: Article

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