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Volumn 138, Issue 11, 2016, Pages 3863-3875

Enantiodivergent Fluorination of Allylic Alcohols: Data Set Design Reveals Structural Interplay between Achiral Directing Group and Chiral Anion

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSTS; ENANTIOSELECTIVITY; FLUORINATION; FLUORINE; FREE ENERGY; HALOGENATION; PHOSPHORIC ACID; STATISTICS; SUBSTRATES;

EID: 84962045450     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.6b00356     Document Type: Article
Times cited : (114)

References (126)
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    • For the entirety of this article, we have defined the result in Figure 1 B as the standard enantioselectivity (i.e. the (S)-catalyst affords the (S)-product). On the basis of this convention, the predominant formation of the (R)-product was considered "negative" when using the (S)-catalyst. Similarly, if use of the (R)-catalyst results in the (S) enantiomer as the major product, this result is considered "negative". This convention was opted as it better alerts the reader to the fact that the enantioselectivity inversion is independent of the catalyst enantiomer used (as opposed to the (R) and (S) terminology)
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