在Pd II / Cu(II)羧酸盐/ CO的存在下,依靠双重C–N键裂解策略,可实现具有高结构和功能多样性的胍衍生物的高效非酶分解为苯胺产物。在这种分解过程中,Pd II物质,Cu(II)羧酸盐和CO的协同作用不仅提供N-酰化剂,而且还提供引发该C–N键裂解序列的引发剂。目前的结果表明,Pd II / Cu(II)羧酸盐/ CO系统为非反应性C–N单键的高选择性裂解提供了一种方便实用的方法。
Copper-Catalyzed Guanidinylation of Aryl Iodides: The Formation of N,N′-Disubstituted Guanidines
摘要:
A copper-catalyzed cross-coupling reaction of guanidine nitrate with aryl iodides was used for the formation of N,N'-disubstituted guanidines to be used as potential therapeutics for strokes. A relatively inexpensive commercially available guanidine salt and a series of aryl iodides together with copper iodide and N,N-diethylsalicylamide as an efficient catalyst/ligand system provided a simple diarylation procedure.
Regenerable solvent mixtures for acid-gas separation
申请人:Research Triangle Institute
公开号:US10960345B2
公开(公告)日:2021-03-30
A solvent system for the removal of acid gases from mixed gas streams is provided. Also provided is a process for removing acid gases from mixed gas streams using the disclosed solvent systems. The solvent systems may be utilized within a gas processing system.
Cleavage of C–N bonds in guanidine derivatives and its relevance to efficient C–N bonds formation
作者:Denghu Chang、Dan Zhu、Peng Zou、Lei Shi
DOI:10.1016/j.tet.2015.01.050
日期:2015.3
nonenzymatic decomposition of guanidine derivatives with high structural and functional diversity into anilide products is achieved in the presence of PdII/Cu(II) carboxylates/CO, relying on a dual C–N bonds cleavage strategy. In this decomposition process, the cooperative action of PdII species, Cu(II) carboxylates, and CO provides not only the N-acylating agents but also an initiator to trigger this
在Pd II / Cu(II)羧酸盐/ CO的存在下,依靠双重C–N键裂解策略,可实现具有高结构和功能多样性的胍衍生物的高效非酶分解为苯胺产物。在这种分解过程中,Pd II物质,Cu(II)羧酸盐和CO的协同作用不仅提供N-酰化剂,而且还提供引发该C–N键裂解序列的引发剂。目前的结果表明,Pd II / Cu(II)羧酸盐/ CO系统为非反应性C–N单键的高选择性裂解提供了一种方便实用的方法。
Copper-Catalyzed Guanidinylation of Aryl Iodides: The Formation of <i>N,N′</i>-Disubstituted Guanidines
作者:Michelle Cortes-Salva、Be-Lan Nguyen、Javier Cuevas、Keith R. Pennypacker、Jon C. Antilla
DOI:10.1021/ol1002175
日期:2010.3.19
A copper-catalyzed cross-coupling reaction of guanidine nitrate with aryl iodides was used for the formation of N,N'-disubstituted guanidines to be used as potential therapeutics for strokes. A relatively inexpensive commercially available guanidine salt and a series of aryl iodides together with copper iodide and N,N-diethylsalicylamide as an efficient catalyst/ligand system provided a simple diarylation procedure.