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|Type:||Artigo de periódico|
|Title:||An Easy And Efficient Method To Produce γ-amino Alcohols By Reduction Of β-enamino Ketones|
|Abstract:||Reduction of β-enamino ketones 2 with NaBH4 in glacial acetic acid gave γ-amino alcohols 1 in 70% to 98% yield with diastereomeric excesses, preferentially the syn product, from 44% to 90%. The stereochemistry of these compounds was confirmed by analysis of their tetrahydro-1,3-oxazine derivatives 3.|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
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