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一种简洁且以多样性为导向的SAG衍生物合成方法。

A concise and diversity-oriented approach to the synthesis of SAG derivatives.

作者信息

Wang Nengdong, Xiang Jing, Ma Zhibo, Quan Junmin, Chen Jiahua, Yang Zhen

机构信息

Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Peking University, Beijing, 100871, China.

出版信息

J Comb Chem. 2008 Nov-Dec;10(6):825-34. doi: 10.1021/cc800025n. Epub 2008 Aug 28.

Abstract

An efficient and rapid solution-phase combinatorial synthesis of the SAG library was developed. The salient features for this library synthesis is the application of carbothioamide-derived palladacycle-catalyzed Suzuki coupling reactions for the parallel synthesis of a series of pyridine-based biaryl aldehydes under aerobic conditions and a direct N-alkylation of carbamates using NaH as base in DMF in the presence of catalytic amount of water. The resultant library has been submitted to biological screening to evaluate their potential role in the regulation of Hedgehog pathway.

摘要

开发了一种高效、快速的SAG文库溶液相组合合成方法。该文库合成的显著特点是应用基于碳硫酰胺的钯环催化铃木偶联反应,在有氧条件下平行合成一系列吡啶基联芳醛,以及在催化量水存在下,以NaH为碱,在DMF中对氨基甲酸酯进行直接N-烷基化反应。所得文库已提交进行生物筛选,以评估它们在刺猬信号通路调控中的潜在作用。

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