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烯丙基硫醚是水相交叉复分解反应中的优势底物:用于位点选择性蛋白质修饰。

Allyl sulfides are privileged substrates in aqueous cross-metathesis: application to site-selective protein modification.

作者信息

Lin Yuya A, Chalker Justin M, Floyd Nicola, Bernardes Gonçalo J L, Davis Benjamin G

机构信息

Chemistry Research Laboratory, Department of Chemistry, University of Oxford, 12 Mansfield Road, Oxford OX1 3TA, U.K.

出版信息

J Am Chem Soc. 2008 Jul 30;130(30):9642-3. doi: 10.1021/ja8026168. Epub 2008 Jul 1.

Abstract

Allyl sulfides undergo efficient cross-metathesis in aqueous media with Hoveyda-Grubbs second generation catalyst 1. The high reactivity of allyl sulfides in cross-metathesis was exploited in the first examples of cross-metathesis on a protein surface. S-Allylcysteine was incorporated chemically into the protein, providing the requisite allyl sulfide handle. Preliminary efforts to genetically incorporate S-allylcysteine into proteins are also reported.

摘要

烯丙基硫醚在水性介质中与第二代霍维达-格鲁布斯催化剂1能高效地进行交叉复分解反应。烯丙基硫醚在交叉复分解反应中的高反应活性被应用于蛋白质表面交叉复分解反应的首个实例中。S-烯丙基半胱氨酸通过化学方法被引入到蛋白质中,提供了所需的烯丙基硫醚基团。本文还报道了将S-烯丙基半胱氨酸基因编码到蛋白质中的初步研究成果。

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