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首页> 外文期刊>Tetrahedron, Asymmetry: The International Journal for Repid Publication on all Aspects of Asymmetry in Orgainc, Inorganic, Organometallic, Physical and Bio-Organic Chemistry >Stereospecific synthesis and absolute configuration of the (2S,3S,4S)-isomer of 2-methyl-2-(carboxycyclopropyl)glycine (MCCG)
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Stereospecific synthesis and absolute configuration of the (2S,3S,4S)-isomer of 2-methyl-2-(carboxycyclopropyl)glycine (MCCG)

机译:2-甲基-2-(羧基环丙基)甘氨酸(MCCG)的(2S,3S,4S)异构体的立体定向合成和绝对构型

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摘要

The conformationally restricted metabotropic glutamate receptor antagonist (2S,3S,4S)-2-methyl-2-(carboxycyclopropyl)glycine 1 (MCCG) has been synthesized in a stereoselective manner (>99% ee) with the (2S 3S,4S) absolute configuration of this molecule being confirmed by X-ray crystallographic analysis. Subsequent physico-chemical studies were undertaken and the data are at odds with those of the commercially available product. (C) 2003 Elsevier Science Ltd. All rights reserved. [References: 15]
机译:构象受限的代谢型谷氨酸受体拮抗剂(2S,3S,4S)-2-甲基-2-(羧基环丙基)甘氨酸1(MCCG)已与(2S 3S,4S)以立体选择性方式(> 99%ee)合成通过X射线晶体学分析证实了该分子的绝对构型。随后进行了理化研究,数据与市售产品不一致。 (C)2003 Elsevier ScienceLtd。保留所有权利。 [参考:15]

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