Synthesis of 1,3-Oxaselenan-2-imines from Isoselenocyanates

G. Sommen, H. Heimgartner
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引用次数: 7

Abstract

The reactions ofaryl isoselenocyanates 1 with 3-chloropropan- 1-ol (8) in the presence of sodium hydride in dichloromethane at room temperature gave 1,3-oxaselenan-2-imines 10 in fair yield. A reaction mechanism via nucleophilic attack of the alcoholate at the isoselenocyanate 1, followed by an 6-exo-teτ cyclization, is most likely.
由异硒氰酸酯合成1,3-草甘膦-2-亚胺
异硒氰酸芳基1与3-氯丙- 1-醇(8)在氢化钠存在下,在室温下在二氯甲烷中反应得到产率相当的1,3-草二烯酸-2-亚胺10。最可能的反应机制是通过醇酯在异硒氰酸酯1上的亲核攻击,然后是6-外显子teτ环化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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