Synthesis of the unnatural amino acid AGDHE, a constituent of the cyclic depsipeptides callipeltins A and D.

Synthesis of the unnatural amino acid AGDHE, a constituent of the cyclic depsipeptides callipeltins A and D.
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非天然氨基酸 AGDHE 的合成,它是环状缩酚肽 callipeltins A 和 D 的组成部分。

DOI:
10.1021/ol0269852
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发表时间:
2002
期刊:
影响因子:
5.2
通讯作者:
Lipton,MarkA
Lipton,MarkA
中科院分区:
化学1区
文献类型:
--
作者:
Thoen,JasonC;Morales-Ramos,AngelI;Lipton,MarkA

文献摘要

相似文献

以受保护的1-鸟氨酸衍生物为原料,经13步反应(总收率15%)合成了新的氨基酸残基(2R,3R,4S)-4-amido-7-guanidino-2,3-dihydroxyheptanoic酸(AGDHE,3)及其(2S,3S,4S)非对映异构体,并用核磁共振氢谱对其构型进行了重新鉴定。
The novel amino acid residue (2R,3R,4S)-4-amido-7-guanidino-2,3-dihydroxyheptanoic acid (AGDHE,3), a constituent of the cyclic depsipeptides callipeltins A and D, and its (2S,3S,4S) diastereomer were synthesized from a protectedl-ornithine derivative in 13 steps (15% overall yield), and its configurational assignment was reexamined by1H NMR.