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filingDate 2009-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2012-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2012508722-A
titleOfInvention Chiral ligand
abstract Formula (1): [wherein R 1 is C 1 -C 8 -alkyl, unsubstituted cyclopentyl, cyclohexyl, norbornyl or adamantyl, or 1 to 3 C 1 -C 4 -alkyl or C 1 -C Cyclopentyl or cyclohexyl substituted by 4 -alkoxy, or unsubstituted or 1-3 C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -fluoroalkyl or C 1 -C 4 - fluoroalkoxy, F and benzyl substituted by Cl, phenyl, naphthyl and anthryl, R 2 and R 3 are each independently at C- bonded hydrocarbon group or heterocyclic hydrocarbon group There, R 4 is, C 1 -C 4 - alkyl, cyclopentyl, cyclohexyl, phenyl, methylphenyl, Mechiruben A method for preparing a ligand of a is] le or benzyl, (a) Formula (A): wherein the compound of R 4 are as defined above), ortho amine side chains Stereoselectively metallized with a dihalide of formula R 1 -PX2 where R 1 is as defined above and X is Cl or Br, and stereoselective hydrolysis results in SPO. To obtain a compound of formula (1) by reaction with a secondary phosphine of formula H-PR 2 R 3, where R 2 and R 3 are as defined above. Obtaining. Novel ligands and their metal complexes obtained by this method.
priorityDate 2008-11-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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