Abstract
The anions from β-keto esters or β-diketones were reacted with diethyl phosphorochloridate to yield the corresponding enol phosphates. These enol phosphates were coupled with dialkylcuprates to produce the β-substituted α,β-unsaturated esters or ketones in good yield. Starting from acyclic β-keto esters this sequence was used to stereoselectively generate tri- and tetrasubstituted olefins.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
169 articles.
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