Enantioselective catalyses .110. new chiral phosphanes derived from substituted quinolines

Brunner, Henri and Rückert, T. (1997) Enantioselective catalyses .110. new chiral phosphanes derived from substituted quinolines. SYNTHESIS-STUTTGART, 1997 (11). pp. 1309-1314. ISSN 0039-7881, 1437-210X

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Abstract

Optically active, two-layer phosphanes were obtained by reaction of quinolineamines with metalated 1,2-bisphosphanylbenzene and chiral monodentate quinolinephosphanes were synthesized by reaction of optically active quinolineamines with lithium diphenylphosphide. The precursors were built up from quinoline derivatives containing bromomethyl groups and chiral secondary amines.

Item Type: Article
Uncontrolled Keywords: ASYMMETRIC HYDROGENATION; ACID; DERIVATIVES; COMPLEXES; LIGANDS; METAL; chiral two-layer phosphanes derived from optically; active quinolineamines
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Anorganische Chemie > Alumni or Retired Professors > Prof. Dr. Henri Brunner
Depositing User: Dr. Gernot Deinzer
Date Deposited: 28 Mar 2023 06:15
Last Modified: 28 Mar 2023 06:15
URI: https://pred.uni-regensburg.de/id/eprint/50463

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