首页> 外文期刊>Organic letters >Asymmetric Phase-Transfer Catalysts Bearing Multiple Hydrogen-Bonding Donors: Highly Efficient Catalysts for Enantio- and Diastereoselective Nitro-Mannich Reaction of Amidosulfones
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Asymmetric Phase-Transfer Catalysts Bearing Multiple Hydrogen-Bonding Donors: Highly Efficient Catalysts for Enantio- and Diastereoselective Nitro-Mannich Reaction of Amidosulfones

机译:带有多个氢键供体的不对称相转移催化剂:酰胺砜对映和非对映选择性硝基曼尼希反应的高效催化剂

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摘要

Bifunctional asymmetric phase-transfer catalysts bearing multiple hydrogen-bonding donors have rarely been explored. The first quaternary ammonium type of these catalysts derived from cinchona alkaloids were readily prepared and found to be highly efficient catalysts for asymmetric nitro-Mannich reactions of amidosulfones. Compared with previous reports, very broad substrate generality was observed, and both enantiomers of the products were achieved in high enantio- and diastereoselectivity (90-99% ee, 13:1 to 99:1 dr).
机译:带有多个氢键供体的双官能不对称相转移催化剂很少被研究。这些衍生自金鸡纳生物碱的催化剂的第一季铵类型很容易制备,并被发现是酰胺砜不对称硝基-曼尼希反应的高效催化剂。与以前的报道相比,观察到非常广泛的底物通用性,并且产物的两种对映异构体均以高对映体和非对映体选择性获得(90-99%ee,13:1至99:1 dr)。

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