Chiral synthons for 2-amino alcohols. Facile preparation of optically active amino hydroxy acids of biological interest.
作者： Tadao Ishizuka , Seigo Ishibuchi , Takehisa Kunieda
DOI: 10.1016/S0040-4020(01)80540-8
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摘要: Abstract A promising method for the versatile synthesis of chiral 2-amino alcohols is provided by enantioselective functionalization olefinic moiety simple heterocycle, 2-oxazolone, involving a stereodefined introduction easily replaceable groups followed stepwise substitution. Versatility this shown in unusual hydroxy amino acids such as statine and hydroxyglutamic acid, which are key components bioactive peptides.
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