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- W2953264725 endingPage "976" @default.
- W2953264725 startingPage "970" @default.
- W2953264725 abstract "Highly electrophilic dichlorofluoromethyl aryl ketones were obtained by oxidation of dichlorofluoromethyl aryl alcohols. Subsequent dechlorination of these ketones using sodium formaldehyde sulfoxylate (Rongalite) and reductive dehalogenating system SnCl2/Al led to various fluoromethyl aryl ketones and chlorofluoromethyl aryl ketones, respectively. Asymmetric reductions of these fluorinated ketones using the inexpensive baker's yeast produced the corresponding fluoromethyl aryl alcohols with different enantioselectivities." @default.
- W2953264725 created "2019-06-27" @default.
- W2953264725 creator A5008348778 @default.
- W2953264725 creator A5086825402 @default.
- W2953264725 creator A5089293192 @default.
- W2953264725 date "2007-01-01" @default.
- W2953264725 modified "2023-09-28" @default.
- W2953264725 title "New synthetic routes towards various α-fluorinated aryl ketones and their enantioselective reductions using baker's yeast" @default.
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- W2953264725 doi "https://doi.org/10.1016/j.tet.2006.11.019" @default.
- W2953264725 hasPublicationYear "2007" @default.
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