Decarbonylative approach to the synthesis of enamides from amino acids: stereoselective synthesis of the (Z)-aminovinyl-D-cysteine unit of mersacidin.
Decarbonylative approach to the synthesis of enamides from amino acids: stereoselective synthesis of the (Z)-aminovinyl-D-cysteine unit of mersacidin.
复制标题
DOI:
10.1021/ol203399x
复制
发表时间:
2012-02-17
期刊:
影响因子:
5.2
通讯作者:
VanNieuwenhze MS
中科院分区:
文献类型:
--
作者:
García-Reynaga P;Carrillo AK;VanNieuwenhze MS
The Pd- and Ni-promoted decarbonylation of amino acid thioesters proceeds smoothly to yield enamides. The synthesis of the (S)-(Z)-AviMeCys subunit of mersacidin, an MRSA-active lantibiotic, via this approach, is described.
登录
查看更多内容
影响因子:
5.2
作者:
Banerjee, Biplab;Litvinov, Dmitry N.;Kang, Junghoon;Bettale, Jennifer D.;Castle, Steven L.
通讯作者:
Castle, Steven L.
影响因子:
2.1
作者:
CRISP, GT;BUBNER, TP
通讯作者:
BUBNER, TP
影响因子:
3.6
作者:
Wang, X;Porco, JA
通讯作者:
Porco, JA
DOI:
10.1039/c39910000627
发表时间:
1991-05-01
影响因子:
--
作者:
WENKERT, E;CHIANELLI, D
通讯作者:
CHIANELLI, D
影响因子:
15
作者:
Yang, Hao;Li, Hao;Liebeskind, Lanny S.
通讯作者:
Liebeskind, Lanny S.