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一种用于不对称氮杂-Henry反应的新型双硫脲有机催化剂。

A Novel Bis-Thiourea Organocatalyst for the Asymmetric Aza-Henry Reaction.

作者信息

Rampalakos Constantinos, Wulff William D

机构信息

Department of Chemistry, Michigan State University, East Lansing, Michigan 48824.

出版信息

Adv Synth Catal. 2008 Aug 4;350(11-12):1785-1790. doi: 10.1002/adsc.200800214.

Abstract

A novel bis-thiourea BINAM-based catalyst for the asymmetric aza-Henry reaction has been developed. This catalyst promotes the reaction of -Boc imines with nitroalkanes to afford β-nitroamines with good yields and high enantioselectivities. This catalyst has the advantage that it can be prepared in a single step from commercially available materials. A model is proposed for the catalyst action where the both components of the reaction are activated simultaneously by hydrogen bonding. Regardless of the mechanism, the success of the present catalyst demonstrates the potential of bis-thioureas as an interesting class of relatively unexplored catalysts.

摘要

一种新型的基于双硫脲 BINAM 的催化剂已被开发用于不对称氮杂-Henry 反应。该催化剂能促进 -Boc 亚胺与硝基烷烃的反应,以良好的产率和高对映选择性得到 β-硝基胺。这种催化剂的优点是可以从市售原料一步制备而成。提出了一种催化剂作用模型,其中反应的两个组分通过氢键同时被活化。无论其作用机理如何,本催化剂的成功都证明了双硫脲作为一类相对未被充分探索的有趣催化剂的潜力。

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