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|Type:||Artigo de periódico|
|Title:||Enantioselective Total Synthesis Of (-)-ericanone|
De Lucca Jr. E.C.
|Abstract:||The first total synthesis of (-)-ericanone was achieved in 10 steps with a 16% overall yield from p-hydroxybenzaldehyde. Notable features of this stereocontrolled approach include a Keck allylation to install the stereocenter at C3 and a 1,5-anti aldol reaction to install the hydroxyl group at C7. © 2012 Elsevier Ltd. All rights reserved.|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
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