The physico-chemical properties of cinchona alkaloids responsible for their unique performance in chiral catalysis

Topics in Catalysis

Volumn 48, Issue 1-4, 2008, Pages 120-127

  Mink, Larry ^b   Ma, Zhen ^a   Olsen, Ryan A ^a   James, Joanna N ^c   Sholl, David S ^c   Mueller, Leonard J ^a   Zaera, Francisco ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b CALIFORNIA STATE UNIVERSITY   (United States)

^c CARNEGIE MELLON UNIVERSITY   (United States)

Author keywords

Adsorption; Chiral catalysis; Cinchona alkaloids; Enantioselectivity; In situ infrared spectroscopy; Protonation; Rotational conformers; Solubility

Indexed keywords

ACTIVE SITE; ADSORPTION BEHAVIOR; CHIRAL CATALYSIS; CHIRAL ENVIRONMENT; CINCHONA ALKALOID; CINCHONA ALKALOIDS; COMPARATIVE STUDIES; COUNTER ANIONS; ENANTIOSELECTIVE; IN-SITU; LIQUID PHASE; METAL SURFACES; MOLECULAR GROUPS; NITROGEN ATOM; PERIPHERAL POSITIONS; PHYSICOCHEMICAL PROPERTY; QUINUCLIDINES; RAPID ADSORPTION; ROTATIONAL CONFORMERS; SOLID SURFACE;

ADSORPTION; CATALYSIS; CHEMICAL PROPERTIES; ENANTIOSELECTIVITY; INFRARED SPECTROSCOPY; ISOMERIZATION; METABOLITES; NITROGEN COMPOUNDS; PROTONATION; SOLUBILITY; STEREOCHEMISTRY;

CONFORMATIONS;

EID: 55549100733     PISSN: 10225528     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11244-008-9041-z     Document Type: Conference Paper

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