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.
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DOI:
10.1021/ol203399x
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发表时间:
2012-02-17
期刊:
影响因子:
5.2
通讯作者:
VanNieuwenhze MS
VanNieuwenhze MS
中科院分区:
化学1区
文献类型:
--
作者:
García-Reynaga P;Carrillo AK;VanNieuwenhze MS

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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.
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