An in Situ Directing Group Strategy for Chiral Anion Phase-Transfer Fluorination of Allylic Alcohols

Journal of the American Chemical Society

Volumn 136, Issue 37, 2014, Pages 12864-12867

  Zi, Weiwei ^a   Wang, Yi Ming ^a   Toste, F Dean ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HALOGENATION;

ALLYLIC ALCOHOL; DIRECTING GROUPS; ENANTIOSELECTIVE; HOMOALLYLIC ALCOHOL; MECHANISTIC STUDIES; PHASE-TRANSFER CONDITIONS; SITU GENERATION; TRANSITION STATE;

FLUORINATION;

ALCOHOL DERIVATIVE; ALKENE; ALLYL COMPOUND; AMIDE; ANION; BORONIC ACID DERIVATIVE; CARBON; FLUORINE; HYDROXYL GROUP; PHENOL; ALLYL ALCOHOL; PROPANOL;

ARTICLE; ASYMMETRIC SYNTHESIS; CATALYSIS; CATALYST; CHEMICAL BOND; ELECTROPHILICITY; ENANTIOSELECTIVITY; FLUORINATION; HYDROGEN BOND; ION TRANSPORT; PROTON TRANSPORT; CHEMICAL STRUCTURE; CHEMISTRY; HALOGENATION; STEREOISOMERISM;

ANIONS; HALOGENATION; MODELS, MOLECULAR; PROPANOLS; STEREOISOMERISM;

EID: 84918774922     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja507468u     Document Type: Article

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