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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Asymmetric synthesis of aziridine 2-phosphonates and azirinyl phosphonates from enantiopure sulfinimines
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Asymmetric synthesis of aziridine 2-phosphonates and azirinyl phosphonates from enantiopure sulfinimines

机译:从对映体纯的亚磺酸亚胺中不对称合成氮丙啶2-膦酸酯和氮丙啶膦酸酯

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摘要

Enantiopure sulfinimine (S)-4 was employed in a Darzens-type synthesis of aziridine 2-phosphonates (-)-7/(+)-8 which were transformed into alpha-amino phosphonates (S)-11/(R)-12 and the first enantiopure examples of azirinyl phosphonates 13-15. (C) 1998 Elsevier Science Ltd. All rights reserved. [References: 28]
机译:对映体纯亚磺胺(S)-4用于氮丙啶2-膦酸酯(-)-7 /(+)-8的Darzens型合成,将其转变为α-氨基膦酸酯(S)-11 /(R)-12以及氮丙啶基膦酸酯13-15的第一个对映纯实例。 (C)1998 Elsevier ScienceLtd。保留所有权利。 [参考:28]

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