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|Type:||Artigo de periódico|
|Title:||1,5-asymmetric Induction In Boron-mediated Aldol Reactions Of β-oxygenated Methyl Ketones|
|Abstract:||This tutorial review describes that high levels of substrate-controlled, 1,5-stereoinduction are obtained in the boron-mediated aldol reactions of β-oxygenated methyl ketones with achiral and chiral aldehydes. Remote induction from the boron enolates gives the 1,5-anti adducts, with the enolate π-facial selectivity critically dependent upon the nature of the β-alkoxy protecting group. This 1,5-anti aldol methodology has been strategically employed in the total synthesis of several natural products with remarkable pharmacological activities. At present, the origin of the high level of 1,5-anti induction obtained with the boron enolates is unclear, although a model based on hydrogen bonding between the β-alkoxy oxygen and the formyl aldehyde hydrogen has recently been proposed. © The Royal Society of Chemistry 2008.|
|Citation:||Chemical Society Reviews. , v. 37, n. 3, p. 451 - 469, 2008.|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
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