New class of β-aminoalcohol ligands derived from isosorbide and isomannide: Application in hydrogen transfer reduction of prochiral ketones

Tetrahedron

Volumn 66, Issue 46, 2010, Pages 8893-8898

  Le, Tin Thanh ^a   Guillarme, Stéphane ^a   Saluzzo, Christine ^a  

^a UNIVERSITÉ DU MAINE   (France)

Author keywords

Aminoalcohols; Asymmetric hydrogen transfer reduction; Biomass; Enantioselective catalysis; Homogeneous catalysis

Indexed keywords

ACETOPHENONE; AMINOALCOHOL; EPOXIDE; ISOMANNIDE; ISOSORBIDE; LIGAND; MANNITOL; RUTHENIUM COMPLEX; STARCH; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC CATALYSIS; CHIRALITY; ELECTRON TRANSPORT; ENANTIOSELECTIVITY; PRIORITY JOURNAL; REACTION OPTIMIZATION; REACTION TIME; REDUCTION; RING OPENING; STEREOCHEMISTRY; SYNTHESIS; TEMPERATURE;

EID: 77958191132     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.09.060     Document Type: Article

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