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|Type:||Artigo de periódico|
|Title:||Hyphenating the Curtius Rearrangement with Morita-Baylis-Hillman Adducts: Synthesis of Biologically Active Acyloins and Vicinal Aminoalcohols|
|Abstract:||Using Morita-Baylis-Hillman adducts as substrates, the Curtius rearrangement was performed in a sequence that allowed the synthesis of several hydroxy-ketones (acyloins) with great structural diversity and in good overall yields. These acyloins in turn were easily transformed into 1,2-anti aminoalcohols through a highly diastereoselective reductive amination step. The synthetic utility of these approaches was exemplified by performing the syntheses of (+/-)-bupropion, a drug used to treat the abstinence syndrome of smoker and (+/-)-spisulosine, a potent anti-tumoral compound originally isolated from a marine source.|
|Editor:||Soc Brasileira Quimica|
|Citation:||Journal Of The Brazilian Chemical Society. Soc Brasileira Quimica, v. 22, n. 8, n. 1568, n. U330, 2011.|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
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