Enantioselective Michael addition catalyzed by cinchona alkaloids

Chirality

Volumn 13, Issue 10, 2001, Pages 614-618

  Szöllösi, György ^a   Bartók, Mihály ^a  

^a UNIVERSITY OF SZEGED   (Hungary)

Author keywords

ketoesters; Cinchona alkaloids; Enantioselectivity; Methyl vinyl ketone; Michael addition

Indexed keywords

CARBOXYLIC ACID DERIVATIVE; CINCHONA ALKALOID; ESTER DERIVATIVE; ETHYL 2 OXOCYCLOHEXANECARBOXYLATE; ETHYL 2 OXOCYCLOPENTANECARBOXYLATE; KETONE; METHYL GROUP; UNCLASSIFIED DRUG;

CATALYSIS; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONFERENCE PAPER; ENANTIOMER; GAS CHROMATOGRAPHY; NUCLEAR MAGNETIC RESONANCE; OPTICAL ROTATION; PRIORITY JOURNAL; REACTION ANALYSIS;

BUTANONES; CATALYSIS; CINCHONA ALKALOIDS; ESTERS; GAS CHROMATOGRAPHY-MASS SPECTROMETRY; MAGNETIC RESONANCE SPECTROSCOPY; METHODS; STEREOISOMERISM;

EID: 0035155508     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/chir.10000     Document Type: Conference Paper

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