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几种手性α-乙酰氨基-β-芳基丙烯酸类化合物的合成 被引量:1

Synthesis of new types of chiral α-acetylamino-β-aryl acrylic acid compounds
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摘要 以乙酰甘氨酸和苯甲醛及其衍生物为原料 ,合成了一系列含碳碳双键的前手性底物 ,(Z) -2 -乙酰氨基苯丙烯酸、(Z) -2 -乙酰氨基 -3 -(对甲氧苯基 ) -丙烯酸、(Z) -2 -乙酰氨基 -3 -(对氯苯基 ) -丙烯酸、(Z) -2 -乙酰氨基 -3 -(间氯苯基 ) -丙烯酸、(Z) -2 -乙酰氨基 -3 -(间硝基苯基 ) -丙烯酸。后 4种是新的有机化合物。产物结构经过核磁共振。 Through the reaction of acetylaminoacetic acid with benzaldehyde,and its derivatives,a series of pre-chiral substrates including CC double bond were synthesized;(Z)-2-acetylamino phenyl acrylic acid,(Z)-2-acetylamino-3-(p-methoxyphenyl) acrylic acid,(Z)-2-acetylamino-3-(p-chloro-phenyl) acrylic acid,(Z)-2-acetylamino-3-(m-chloro-phenyl) acrylic acid,and (Z)-2-acetylamino-3-(m-nitro-phenyl) acrylic acid.All the above compounds except the first one are new organic compounds.The products were proved right by unclear magnetic resonance and mass spectrometry.
作者 陈晓彬
出处 《化学试剂》 CAS CSCD 北大核心 2002年第6期365-366,共2页 Chemical Reagents
关键词 手性α-乙酰氨基-β-芳基丙烯酸 合成 (Z)-2-乙酰氨基-3-(间氯苯基)-丙烯酸 (Z)-2-乙酰氨基-3-(间硝基苯基)-丙烯酸 不对称催化 Z)-2-acetylamino phenyl acrylic acid,(Z)-2-acetylamino-3-(p-methoxypheny) acrylic acid,(Z)-2-acetylamino-3-(p-chloro-phenyl) acrylic acid,(Z)-2-acetylamino-3-(m-chloro-phenyl) acrylic acid,(Z)-2-acetylamino-3-(m-nitro-phenyl) acrylic acid,organ
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同被引文献9

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