Synthetic studies toward the mannopeptimycins: synthesis of orthogonally protected beta-hydroxyenduracididines.
Synthetic studies toward the mannopeptimycins: synthesis of orthogonally protected beta-hydroxyenduracididines.
复制标题
甘露肽霉素的合成研究：正交保护的β-羟基enduracididines的合成。
DOI：
10.1021/ol100219a
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发表时间：
2010
期刊：
影响因子：
5.2
通讯作者：
VanNieuwenhze,MichaelS
中科院分区：
文献类型：
--
作者：
Olivier,KevinS;VanNieuwenhze,MichaelS
The asymmetric synthesis of the nonproteinogenic amino acids (2S,3S,4′S)-β-hydroxyenduracididine3and (2R,3S,4′S)-β-hydroxyenduracididine4in orthogonally protected form in 15 total steps from Garner’s aldehyde is reported. The former andN-glycosylated form of the latter are found in the glycopeptide antibiotic mannopeptimycin.
