http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102199125-B

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Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b1b95a0151fe6cf57f119866e3a10c11
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-02
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filingDate 2011-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-07-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e826c71f8064b81f488e99d937027d9a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7b033a53b8fd8fafcc9dbdaf1b9f4a4f
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publicationDate 2012-07-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102199125-B
titleOfInvention Fluorine-containing imidazoline derivatives and preparation method thereof
abstract The invention relates to a fluorine-containing imidazoline derivative and a synthesis method thereof. The structural formula of the compound is: and . (2R,4S)-4-phenyl-1,2-dimethyl-2-trifluoromethyl imidazoline and (2R,4R)-4-phenyl-1,2-dimethyl- 2-Trifluoromethylimidazoline was applied to the aldol condensation reaction, and α, β-dihydroxy ketone compounds could be synthesized with high stereoselectivity. When the reaction substrate aldehyde is an electron-withdrawing aromatic aldehyde, the reaction results show relatively good enantioselectivity, and when the reaction substrate aldehyde is an electron-pushing aromatic aldehyde and aliphatic aldehyde, the reaction result shows relatively poor enantioselectivity sex. The catalyst has a certain application prospect for the aldol condensation reaction.
priorityDate 2011-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Predicate Subject
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Total number of triples: 23.