Direct Guanylation of Amino Groups by Cyanamide in Water: Catalytic Generation and Activation of Unsubstituted Carbodiimide by Scandium(III) Triflate

Tsubokura Kazuki; Iwata Takayuki; Taichi Misako; Kurbangalieva Almira; Fukase Koichi; Nakao Yoichi; Tanaka Katsunori<sup>*</sup>

doi:10.1055/s-0033-1341080

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Direct Guanylation of Amino Groups by Cyanamide in Water: Catalytic Generation and Activation of Unsubstituted Carbodiimide by Scandium(III) Triflate

作者：Tsubokura Kazuki; Iwata Takayuki; Taichi Misako; Kurbangalieva Almira; Fukase Koichi; Nakao Yoichi; Tanaka Katsunori^*

来源：Synlett, 2014, 25(9): 1302-1306.

DOI：10.1055/s-0033-1341080

摘要

Guanylation proceeded efficiently upon treatment of the various amines with cyanamide in the presence of catalytic amounts of scandium(III) triflate under mild conditions. The method did not require the guanylation reagents to be preactivated, and the reaction proceeded efficiently in water. The method, therefore, has practical utility for substrates that dissolve only in aqueous solutions, for example, peptides or pharmacologically important compounds.