The stereoselective construction of E- and Z-Δ-Ile from E-dehydroamino acid ester: the synthesis of the phomopsin A tripeptide side chain.
The stereoselective construction of E- and Z-Δ-Ile from E-dehydroamino acid ester: the synthesis of the phomopsin A tripeptide side chain.
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DOI：
10.1039/c5cc08458j
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发表时间：
2016-01
影响因子：
4.9
通讯作者：
Yoko Yasuno;A. Nishimura;Yoshifumi Yasukawa;Yuma Karita;Y. Ohfune;T. Shinada
中科院分区：
文献类型：
--
作者：
Yoko Yasuno;A. Nishimura;Yoshifumi Yasukawa;Yuma Karita;Y. Ohfune;T. Shinada
The stereoselective synthesis of the phomopsin A tripeptide side chain was achieved by using methyl 2-(((benzyloxy)carbonyl)amino)-2-(diphenoxyphosphoryl)acetate as a common synthetic precursor for the synthesis of E-Δ-dehydroisoleucine and E-Δ-aspartate.
