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银催化苄基C(sp3)—H键与炔丙基C(sp3)—H键的位点选择性胺化

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探讨了一种合成环状氨基磺酸酯的新方法。采用AgClO4/三(2-吡啶基甲基)胺催化体系,催化苄基C(sp3)—H键与炔丙基C(sp3)—H键的分子内位点选择性胺化反应,以89%收率和9。2∶1位点选择性得到了环状氨基磺酸酯。反应具有条件温和、官能团耐受性好、原子经济性和步骤经济性高等优点,为碳氮的构建提供了一种选择策略。
Silver Catalyzed Site-Selective C(sp3)—H Bond Amination of Benzyl Over Propinyl C(sp3)—H Bond
In recent years,construction of C—N bonds through nitrogen source provided by nitrene has become a novel and important synthesis strategy in organic reactions,further-more,these methods have been widely used in pharmaceutical chemistry and total synthesis of natural products.In this paper,the AgClO4/tris(2-pyridylmethyl)amine catalyzed intra-molecular site-selective amination of benzyl C(sp3)—H bond and propinyl C(sp3)—H bond to give the cyclic sulfamates in 89%yields and 9.2∶1 site-selectivity.This reaction has the advantages of mild conditions,good functional group tolerance,high atom economy and step economy,which provides a strategy for the construction of C—N bonds.

silver-catalyzed nitrenesite-selective aminationcyclic sulfamate derivativesbenzyl C(sp3)—H bond

矫鲁振、李延顺、滕大为

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青岛科技大学 化工学院,山东 青岛 266042

山东科技职业学院,山东 潍坊 261021

银催化的氮宾 位点选择性胺化 环状氨基磺酸酯衍生物 苄基C(sp3)—H键

2024

青岛科技大学学报(自然科学版)
青岛科技大学

青岛科技大学学报(自然科学版)

CSTPCD
影响因子:0.297
ISSN:1672-6987
年,卷(期):2024.45(5)