Spontaneous resolution of julia-kocienski intermediates facilitates phase separation to produce Z - And e -monofluoroalkenes

Journal of the American Chemical Society

Volumn 137, Issue 15, 2015, Pages 5199-5203

  Zhao, Yanchuan ^a   Jiang, Fanzhou ^a   Hu, Jinbo ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

BIOACTIVITY; CARBONYL COMPOUNDS; DRUG PRODUCTS; ISOMERS; LIQUIDS; PHASE SEPARATION; SYNTHESIS (CHEMICAL);

BIOLOGICALLY ACTIVE COMPOUNDS; DRUG DEVELOPMENT; KINETIC RESOLUTION; LIQUID-LIQUID EXTRACTION; PHARMACOLOGICAL ACTIVITY; POTENTIAL ANTICANCER AGENTS; SPONTANEOUS RESOLUTION; Z- AND E- ISOMERS;

SEPARATION;

ALDEHYDE; ALKENE DERIVATIVE; CARBONYL DERIVATIVE; HYDROCHLORIC ACID; ALKENE; FLUORINATED HYDROCARBON;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; COLUMN CHROMATOGRAPHY; CRYSTALLOGRAPHY; ENVIRONMENTAL TEMPERATURE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; JULIA KOCIENSKI REACTION; LIQUID LIQUID EXTRACTION; PHASE SEPARATION; CHEMISTRY; ISOLATION AND PURIFICATION; KINETICS; STEREOISOMERISM; SYNTHESIS;

ALKENES; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; HYDROCARBONS, FLUORINATED; KINETICS; LIQUID-LIQUID EXTRACTION; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 84928475895     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.5b02112     Document Type: Article

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