首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >A new efficient enantioselective synthesis of malonylphenylalanyl and malonylmethylphenylalanyl derivatives suitable for solid phase peptide synthesis
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A new efficient enantioselective synthesis of malonylphenylalanyl and malonylmethylphenylalanyl derivatives suitable for solid phase peptide synthesis

机译:适用于固相肽合成的丙二酰基苯丙氨酰基和丙二酰基甲基苯丙氨酰基衍生物的新型高效对映选择性合成

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摘要

A new synthesis of enantiomerically pure malonylphenylalanyl and malonylmethylphenylalanyl derivatives was developed in which the corresponding prochiral enamides were treated by asymmetric hydrogenation using the Rh(I)-(S,S)-Me-DuPHOS system.These unnatural amino acids were suitably protected and can be used in solid phase peptide synthesis.
机译:开发了对映体纯的丙二酰基苯丙氨酰基和丙二酰基甲基苯丙氨酰基衍生物的新合成方法,其中使用Rh(I)-(S,S)-Me-DuPHOS系统通过不对称氢化处理相应的前手性酰胺,对这些非天然氨基酸进行了适当的保护并可以用于固相肽合成。

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