Modular chiral diphosphite derived from l-tartaric acid. Applications in metal-catalyzed asymmetric reactions

Journal of Molecular Catalysis A: Chemical

Volumn 328, Issue 1-2, 2010, Pages 68-75

  Rosas Hernández, Alonso ^a   Vargas Malvaez, Edgar ^a   Martin, Erika ^a   Crespi, Laura ^b   Bayón, J Carles ^b  

^a UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^b UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

Author keywords

Allylic alkylation; Asymmetric catalysis; Chiral diphosphite; Hydroformylation

Indexed keywords

ACTIVE SPECIES; ALLYLIC ALKYLATION; ALLYLIC SUBSTITUTION; ASYMMETRIC CATALYSIS; ASYMMETRIC REACTION; BIPHENYL MOIETY; CATALYTIC SPECIES; CHIRAL DIPHOSPHITE; CONVERSION RATES; COORDINATION PROPERTIES; CYCLIC SUBSTRATES; DIASTEREOISOMERS; DIMETHYL MALONATE; DIPHOSPHITE; KINETIC RESOLUTION; L-TARTARIC ACIDS; METAL ATOMS; PENTACOORDINATED; RHODIUM AND PALLADIUM COMPLEXES; TARTARIC ACIDS;

ACIDS; ALKYLATION; CATALYSIS; ENANTIOSELECTIVITY; HYDROCARBONS; HYDROFORMYLATION; HYDROXYLATION; LIGANDS; PALLADIUM; RHODIUM; RHODIUM COMPOUNDS; STYRENE; SUBSTITUTION REACTIONS; SUBSTRATES;

PALLADIUM COMPOUNDS;

EID: 77955466850     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2010.06.001     Document Type: Article

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