首页> 外文期刊>Journal of the Chemical Society, Perkin Transactions 1 >New synthetic routes to alpha-amino acids and gamma-oxygenated alpha-amino acids. Reductive denitration and oxidative transformations of gamma-nitro-alpha-amino acids
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New synthetic routes to alpha-amino acids and gamma-oxygenated alpha-amino acids. Reductive denitration and oxidative transformations of gamma-nitro-alpha-amino acids

机译:合成α-氨基酸和γ-加氧α-氨基酸的新途径。 γ-硝基-α-氨基酸的还原脱硝和氧化转化

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摘要

Transformation of gamma-nitro-alpha-amino acid derivatives into alpha-amino acids by reductive denitration, into the gamma-oxo-alpha-amino acids by ozonolysis of the corresponding amino acid ester nitronate derivatives, and into gamma-hydroxy-alpha-amino acid derivatives by subsequent reduction of the oxo functionality, can be achieved in good yields. As the gamma-nitro-alpha-amino acid derivatives are prepared from N,O-protected dehydroalanines derivable from the corresponding alanine, serine and cysteine derivatives by specific routes, the overall procedures provide a means for selective conversion of these simple alpha-amino acids into more complex ones. [References: 52]
机译:通过还原性反硝化作用将γ-硝基-α-氨基酸衍生物转变为α-氨基酸,通过相应的氨基酸酯亚硝酸盐衍生物的臭氧分解,转变为γ-氧代-α-氨基酸,转变为γ-羟基-α-氨基酸通过随后降低氧代官能度可得到高产率的酸衍生物。由于γ-硝基-α-氨基酸衍生物是通过特定路线由可衍生自相应丙氨酸,丝氨酸和半胱氨酸衍生物的N,O保护的脱氢丙氨酸制备的,因此整个程序提供了选择性转化这些简单α-氨基酸的方法变成更复杂的[参考:52]

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