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在温和条件下由伯胺和二氧化碳合成氰基甲酰胺。合成角蛋白胺。

Synthesis of cyanoformamides from primary amines and carbon dioxide under mild conditions. Synthesis of ceratinamine.

作者信息

García-Egido Eduardo, Paz Jairo, Iglesias Beatriz, Muñoz Luis

机构信息

Departamento de Química Orgánica, Facultade de Química, Universidade de Vigo, 36310 Vigo, Spain.

出版信息

Org Biomol Chem. 2009 Oct 7;7(19):3991-9. doi: 10.1039/b912043b. Epub 2009 Jul 23.

DOI:10.1039/b912043b
PMID:19763302
Abstract

Treatment of primary amines with tetramethylphenylguanidine (PhTMG) and a cyanophosphonate at -10 degrees Celsius under an atmosphere of carbon dioxide provides cyanoformamides in very high to excellent yields. The reaction proceeds efficiently within a short time. By-products were not detected in most runs and epimerization was not found when optically pure alpha-aminoesters were used as substrates. As an example, the reaction was applied to the synthesis of the marine natural product ceratinamine.

摘要

在二氧化碳气氛下,于-10摄氏度用四甲基苯基胍(PhTMG)和氰基膦酸酯处理伯胺,可得到产率非常高至优异的氰基甲酰胺。该反应在短时间内有效进行。在大多数反应中未检测到副产物,并且当使用光学纯的α-氨基酯作为底物时未发现差向异构化。例如,该反应被应用于海洋天然产物角胺的合成。

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