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首页> 外文期刊>Letters in Organic Chemistry >Synthesis of Chiral 2-(6,8-dichloro-4-methyl-1,1,3-trioxo-3,4-dihydro-1H-1λ6-benzo[1,2,4]thiadiazin-2-yl) Carboxylic Acids Derived from Enantiomeric Amino Acids
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Synthesis of Chiral 2-(6,8-dichloro-4-methyl-1,1,3-trioxo-3,4-dihydro-1H-1λ6-benzo[1,2,4]thiadiazin-2-yl) Carboxylic Acids Derived from Enantiomeric Amino Acids

机译:手性2-(6,8-二氯-4-甲基-1,1,3-三氧代-3,4-二氢-1H-1λ6-苯并[1,2,4]噻二嗪-2-基)羧酸的合成衍生自对映体氨基酸

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摘要

A series of new chiral 2-(6,8-dichloro-4-methyl-1,1,3-trioxo-3,4-dihydro-1H-1λ6-benzo[1,2,4]thiadiazin-2-yl) carboxylic acids 7a-g containing the chiral amino acid residue were synthesized by adopting the chemical transformations, which have not affected the chirality of the amino acid residue. No significant racemization of the chiral centre was observed during the synthesis of enantiomeric benzothiadiazine 1,1-dioxide derivatives from the corresponding D and L amino acids. Structures of all the newly synthesized compounds were determined by analytical and spectral data.
机译:一系列新的手性2-(6,8-二氯-4-甲基-1,1,3-三氧代-3,4-二氢-1H-1λ6-苯并[1,2,4]噻二嗪-2-基)通过化学转化合成了含有手性氨基酸残基的羧酸7a-g,其不影响氨基酸残基的手性。从相应的D和L氨基酸合成对映体苯并噻二嗪1,1-二氧化物衍生物时,未观察到手性中心的明显消旋。通过分析和光谱数据确定所有新合成的化合物的结构。

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