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甲醛叔丁基腙与α-酮酯的不对称形式羰基-ene 反应:双脲催化剂的双重活化。

Asymmetric formal carbonyl-ene reactions of formaldehyde tert-butyl hydrazone with α-keto esters: dual activation by bis-urea catalysts.

机构信息

Instituto Investigaciones Químicas (CSIC-US), C/Américo Vespucio, 49, 41092 Sevilla, Spain.

出版信息

J Am Chem Soc. 2012 Aug 8;134(31):12912-5. doi: 10.1021/ja305209w. Epub 2012 Jul 26.

Abstract

The dual activation of α-keto esters and formaldehyde tert-butyl hydrazone by BINAM-derived bis-ureas is the key to achieve high reactivity and excellent enantioselectivities in nucleophilic addition (formal carbonyl-ene reaction) to functionalized tertiary carbinols. Ensuing high-yielding diazene-to-aldehyde tranformations and subsequent derivatizations provides a direct entry to a variety of densely functionalized products.

摘要

BINAM 衍生的双脲对 α-酮酯和甲醛叔丁基腙的双重活化是实现亲核加成(醛羰基-ene 反应)到功能化叔醇高反应性和优异对映选择性的关键。随后高产的二氮烯到醛的转化和随后的衍生化提供了直接进入各种高度官能化产物的途径。

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