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Palladium-Catalyzed Hydroaminocarbonylation of Alkynes with Tertiary Amines via C–N Bond Cleavage
Organic Letters ( IF 5.2 ) Pub Date : 2017-11-07 00:00:00 , DOI: 10.1021/acs.orglett.7b03331
Bao Gao 1 , Hanmin Huang 1, 2, 3
Affiliation  

An efficient strategy for the cleavage of the C–N bond of tertiary amines was developed with DTBP as an oxidant, in which the cleaved H atom and amine moiety were successfully transferred to the desired products. This strategy has enabled an efficient palladium-catalyzed hydroaminocarbonylation of alkynes with tertiary amines. Notably, the catalyst loading could be lowered from 5 to 0.1 mol %, which represents the lowest catalyst loading among the reported work on carbonylation via C–N bond activation.

中文翻译:

通过C–N键裂解,钯催化叔胺与炔烃催化的氢氨基羰基化反应

以DTBP为氧化剂,开发了一种有效的叔胺C–N键断裂的策略,其中已断裂的H原子和胺部分已成功转移到所需的产物中。该策略已使炔烃与叔胺有效地进行钯催化的氢氨基羰基化。值得注意的是,催化剂的负载量可以从5 mol%降低到0.1 mol%,这代表了在报告的通过C–N键活化进行羰基化的最低催化剂负载量。
更新日期:2017-11-07
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