Matches in SemOpenAlex for { <https://semopenalex.org/work/W2165067173> ?p ?o ?g. }
- W2165067173 endingPage "4525" @default.
- W2165067173 startingPage "4513" @default.
- W2165067173 abstract "The synthesis, CSP-HPLC resolution, and absolute configuration assignment of a series of 4-dialkylaminopyridine-based atropisomeric biaryls are described. Screening of these enantiomerically pure catalysts, which differ only in the nature of the 4-dialkylamino substituent, for the kinetic resolution of 1-(1-naphthyl)ethanol reveals the importance of this group on the selectivity of catalysis. The di-n-butylamino derivative displays the most favourable catalytic profile. The utility of this catalyst for the kinetic resolution of a selection of sec-alcohols, including a precursor for the synthesis of the antidepressant fluoxetine hydrochloride (Prozac®) are reported. The possible role of the dialkylamino group in chirality transfer is discussed." @default.
- W2165067173 created "2016-06-24" @default.
- W2165067173 creator A5025860787 @default.
- W2165067173 creator A5040804835 @default.
- W2165067173 creator A5048725045 @default.
- W2165067173 creator A5049300795 @default.
- W2165067173 creator A5088510055 @default.
- W2165067173 date "2004-05-01" @default.
- W2165067173 modified "2023-10-16" @default.
- W2165067173 title "New atropisomeric biaryl derivatives of 4-aminopyridine—identification of an improved nucleophilic catalyst for asymmetric acylation of sec-alcohols" @default.
- W2165067173 cites W1976971773 @default.
- W2165067173 cites W1987684252 @default.
- W2165067173 cites W1994983857 @default.
- W2165067173 cites W1998576063 @default.
- W2165067173 cites W2002392171 @default.
- W2165067173 cites W2007884545 @default.
- W2165067173 cites W2009468076 @default.
- W2165067173 cites W2012028316 @default.
- W2165067173 cites W2013890623 @default.
- W2165067173 cites W2017747865 @default.
- W2165067173 cites W2018495952 @default.
- W2165067173 cites W2019042407 @default.
- W2165067173 cites W2020631791 @default.
- W2165067173 cites W2021056577 @default.
- W2165067173 cites W2023278166 @default.
- W2165067173 cites W2027658949 @default.
- W2165067173 cites W2032504638 @default.
- W2165067173 cites W2034802512 @default.
- W2165067173 cites W2038696941 @default.
- W2165067173 cites W2042154265 @default.
- W2165067173 cites W2045002801 @default.
- W2165067173 cites W2048420778 @default.
- W2165067173 cites W2048722894 @default.
- W2165067173 cites W2054934071 @default.
- W2165067173 cites W2064046534 @default.
- W2165067173 cites W2064166025 @default.
- W2165067173 cites W2071047685 @default.
- W2165067173 cites W2076009546 @default.
- W2165067173 cites W2080402976 @default.
- W2165067173 cites W2088595696 @default.
- W2165067173 cites W2089336861 @default.
- W2165067173 cites W2107843175 @default.
- W2165067173 cites W2127649211 @default.
- W2165067173 cites W2949300601 @default.
- W2165067173 cites W2949404125 @default.
- W2165067173 cites W2949482090 @default.
- W2165067173 cites W2949699007 @default.
- W2165067173 cites W2950012646 @default.
- W2165067173 cites W2951430266 @default.
- W2165067173 cites W2952620304 @default.
- W2165067173 cites W2952845563 @default.
- W2165067173 cites W2953148088 @default.
- W2165067173 cites W2953177588 @default.
- W2165067173 cites W4211250522 @default.
- W2165067173 doi "https://doi.org/10.1016/j.tet.2004.01.098" @default.
- W2165067173 hasPublicationYear "2004" @default.
- W2165067173 type Work @default.
- W2165067173 sameAs 2165067173 @default.
- W2165067173 citedByCount "73" @default.
- W2165067173 countsByYear W21650671732012 @default.
- W2165067173 countsByYear W21650671732013 @default.
- W2165067173 countsByYear W21650671732014 @default.
- W2165067173 countsByYear W21650671732015 @default.
- W2165067173 countsByYear W21650671732016 @default.
- W2165067173 countsByYear W21650671732017 @default.
- W2165067173 countsByYear W21650671732018 @default.
- W2165067173 countsByYear W21650671732019 @default.
- W2165067173 countsByYear W21650671732020 @default.
- W2165067173 countsByYear W21650671732022 @default.
- W2165067173 countsByYear W21650671732023 @default.
- W2165067173 crossrefType "journal-article" @default.
- W2165067173 hasAuthorship W2165067173A5025860787 @default.
- W2165067173 hasAuthorship W2165067173A5040804835 @default.
- W2165067173 hasAuthorship W2165067173A5048725045 @default.
- W2165067173 hasAuthorship W2165067173A5049300795 @default.
- W2165067173 hasAuthorship W2165067173A5088510055 @default.
- W2165067173 hasConcept C106159729 @default.
- W2165067173 hasConcept C111771559 @default.
- W2165067173 hasConcept C118792377 @default.
- W2165067173 hasConcept C121332964 @default.
- W2165067173 hasConcept C124668440 @default.
- W2165067173 hasConcept C138268822 @default.
- W2165067173 hasConcept C146686406 @default.
- W2165067173 hasConcept C154945302 @default.
- W2165067173 hasConcept C161790260 @default.
- W2165067173 hasConcept C162324750 @default.
- W2165067173 hasConcept C167981757 @default.
- W2165067173 hasConcept C178790620 @default.
- W2165067173 hasConcept C178907741 @default.
- W2165067173 hasConcept C185592680 @default.
- W2165067173 hasConcept C193557335 @default.
- W2165067173 hasConcept C20621625 @default.
- W2165067173 hasConcept C21951064 @default.
- W2165067173 hasConcept C2778689049 @default.
- W2165067173 hasConcept C28173026 @default.
- W2165067173 hasConcept C41008148 @default.
- W2165067173 hasConcept C52703039 @default.
- W2165067173 hasConcept C62520636 @default.