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在温和条件下由胺和 CO2 平行合成脲和氨基甲酸酯。

Parallel synthesis of ureas and carbamates from amines and CO2 under mild conditions.

机构信息

Department of Chemistry, Merck Research Laboratories, 33 Avenue Louis Pasteur, Boston, Massachusetts 02115, USA.

出版信息

Org Lett. 2010 Mar 19;12(6):1340-3. doi: 10.1021/ol100259j.

Abstract

A mild and efficient library synthesis technique has been developed for the synthesis of ureas and carbamates from carbamic acids derived from the DBU-catalyzed reaction of amines and gaseous carbon dioxide. Carbamic acids derived from primary amines reacted with Mitsunobu reagents to generate isocyanates in situ which were condensed with primary and secondary amines to afford the desired ureas. Similarly, carbamic acids from secondary amines reacted with alcohols activated with Mitsunobu reagents to form carbamates.

摘要

已开发出一种温和且高效的文库合成技术,可用于从 DBU 催化胺与二氧化碳气体反应生成的氨基甲酸衍生的脲和氨基甲酸酯的合成。伯胺衍生的氨基甲酸与 Mitsunobu 试剂反应,原位生成异氰酸酯,然后与伯胺和仲胺缩合,得到所需的脲。类似地,仲胺衍生的氨基甲酸与用 Mitsunobu 试剂活化的醇反应,形成氨基甲酸酯。

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