Stereoselective preparation of lipidated carboxymethyl-proline/pipecolic acid derivatives via coupling of engineered crotonases with an alkylmalonyl-CoA synthetase.

Stereoselective preparation of lipidated carboxymethyl-proline/pipecolic acid derivatives via coupling of engineered crotonases with an alkylmalonyl-CoA synthetase.
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通过工程化巴豆酸酶与烷基丙二酸单酰辅酶A合成酶的偶联,立体选择性地制备脂质化羧甲基脯氨酸/哌可酸衍生物。

DOI:
10.1039/c3ob41525b
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发表时间:
2013
影响因子:
3.2
通讯作者:
Hamed RB
Hamed RB
中科院分区:
化学3区
文献类型:
--
作者:
Hamed RB

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The trisubstituted enolate- and C–C bond-forming capacities of engineered carboxymethylproline synthases CMPSs are coupled with the malonyl-CoA synthetase MatB to enable stereoselective preparation of 5- and 6-membered N-heterocycles functionalised with alkyl-substituted carboxymethyl side chains, starting from achiral alkyl-substituted malonic acids and L-amino acid semialdehydes. The results illustrate the biocatalytic utility of crotonases in tandem enzyme-catalysed reactions for stereoselective synthesis.
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