首页> 外文会议>International Mass Spectrometry Conference >ENANTIOSELECTIVE REDUCTION FROM QUATERNARY COPPER D,L AMINO ACID COMPLEXES: ORIGIN OF THE WEAK CHIRAL EFFECT OBSERVED WITH D/L ASPARTIC AND GLUTAMIC ACIDS
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ENANTIOSELECTIVE REDUCTION FROM QUATERNARY COPPER D,L AMINO ACID COMPLEXES: ORIGIN OF THE WEAK CHIRAL EFFECT OBSERVED WITH D/L ASPARTIC AND GLUTAMIC ACIDS

机译:从季铜D,L氨基酸复合物的对映选择性减少:用D / L天冬氨酸和谷氨酸观察到弱手性效应的来源

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Amino acid enantiomers (AA_L/AA_D) distinction was a challenge solve after the 2000s. A method proposed by G. Cooks (1) was based on (i) electrospray formation of quaternary [2AA'_L+AA_(L/D)H+Cu~(II)]~+ complex diastereomers (AA_L' as reference, AA_(L/D), that of unknown chirality) and (ii) their comparative dissociations by CID. Applying this approach and using AA'_L=phenylglycine, an enantioselective reduction accompanying expected chiral effects were observed (2).
机译:氨基酸对映异构体(AA_L / AA_D)区别在2000年代之后是一种攻击问题。 G.烹饪(1)提出的方法基于(i)季铵的电喷雾形成[2AA'_L + AA_(L / D)H + Cu〜(II)]〜+复合物非对映异构体(AA_L'作为参考,AA_ (L / D),未知的手性)和(ii)CID的比较解剖。应用这种方法并使用AA'_L =苯基甘氨酸,观察到伴随预期的手性效应的对映选择性降低(2)。

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