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N-Boc-aminals as easily accessible precursors for less accessible N-Boc-imines: facile synthesis of optically active propargylamine derivatives using Mannich-type reactions

机译:N-Boc-氨基缩醛作为易获得的N-Boc-亚胺的易于获得的前体:使用曼尼希型反应轻松合成旋光炔丙基胺衍生物

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摘要

We developed a facile and practical synthesis of N-Boc-aminals, which can be used as precursors for less accessible N-Boc-imines. Aminals were obtained via simple dehydration condensation reactions of t-butyl carbamate (BocNH(2)) and various aldehydes in acetic anhydride, followed by filtration and washing with hexane. The obtained N-Boc-alkynylaminals could be successfully applied in enantioselective Mannichtype reactions, catalyzed by chiral phosphoric acids, to afford optically active propargylamine derivatives. (C) 2016 Published by Elsevier Ltd.
机译:我们开发了一种简便实用的N-Boc-氨基缩醛合成方法,可以将其用作难以获得的N-Boc-亚胺的前体。通过氨基甲酸叔丁酯(BocNH(2))和各种醛在乙酸酐中的简单脱水缩合反应,然后过滤并用己烷洗涤,可以得到缩醛。所获得的N-Boc-炔基laminals可以成功地用于手性磷酸催化的对映选择性曼尼希型反应,从而提供光学活性的炔丙基胺衍生物。 (C)2016由Elsevier Ltd.出版

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