2010
DOI: 10.1002/chin.201026127
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ChemInform Abstract: N‐Heterocyclic Carbene Catalyzed Transformations of 3‐Halopropenals to the Equivalents of β‐Acylvinyl Anions.

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“…Additionally, alkyl-substituted ynals and α-keto esters were not described. Concurrently, Ma and co-workers, building on previous work, reported a highly enantioselective [3 + 2] annulation of β-bromo enals and N- protected isatins to furnish spirooxindole-butenolides, catalyzed by a N- heterocyclic carbene catalyst bearing a hydroxyl moiety ( B 28 ) (Scheme ) …”
Section: Catalysis Involving Acylazolium Intermediatesmentioning
confidence: 99%
“…Additionally, alkyl-substituted ynals and α-keto esters were not described. Concurrently, Ma and co-workers, building on previous work, reported a highly enantioselective [3 + 2] annulation of β-bromo enals and N- protected isatins to furnish spirooxindole-butenolides, catalyzed by a N- heterocyclic carbene catalyst bearing a hydroxyl moiety ( B 28 ) (Scheme ) …”
Section: Catalysis Involving Acylazolium Intermediatesmentioning
confidence: 99%