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- W2035862873 abstract "Zinkchlorid machts möglich und katalysiert die enantiospezifische Kreuzkupplung von α-Hydroxyestertriflaten mit Grignard-Reagentien unter milden Bedingungen (siehe Schema). Enantiomerenreine α-Hydroxyester sind direkt aus dem chiralen Pool oder durch die Diazotierung von α-Aminosäuren zugänglich. Beide Reaktionspartner können breit variiert werden, und die Umsetzung verläuft mit umgekehrter Polarität wie die klassische Enolatalkylierung. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2001/2008/z800733_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
- W2035862873 created "2016-06-24" @default.
- W2035862873 creator A5067624195 @default.
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- W2035862873 date "2008-07-07" @default.
- W2035862873 modified "2023-10-17" @default.
- W2035862873 title "Zink‐katalysierte enantiospezifische sp<sup>3</sup>‐sp<sup>3</sup>‐Kreuzkupplung von α‐Hydroxyestertriflaten mit Grignard‐Reagentien" @default.
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- W2035862873 doi "https://doi.org/10.1002/ange.200800733" @default.
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