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Orthoamides by selective borohydride reduction of N,N′,N″-triacyl- and N,N′,N″-tri(alkoxycarbonyl)-guanidines
Tetrahedron Letters ( IF 1.5 ) Pub Date : 2018-12-27 , DOI: 10.1016/j.tetlet.2018.12.060 Matthew C. Davis , Thomas J. Groshens
中文翻译:
通过选择性硼氢化物还原的Orthoamides Ñ,Ñ ',Ñ “-triacyl-和Ñ,Ñ ',Ñ ” -三(烷氧基羰基)-guanidines
更新日期:2018-12-27
Tetrahedron Letters ( IF 1.5 ) Pub Date : 2018-12-27 , DOI: 10.1016/j.tetlet.2018.12.060 Matthew C. Davis , Thomas J. Groshens
N,N′,N″-Triacylguanidines and N,N′,N″-tri(alkoxycarbonyl)guanidines were prepared and reduced with borohydride salts in a mixture of tetrahydrofuran and acetic acid to give triacyl and tri(alkoxycarbonyl) orthoamides in yields of 40–85%. However, similar reduction of N,N′,N″-tri(t-butoxycarbonyl)guanidine did not give orthoamide but the aminal di(t-butyl) methylenedicarbamate.
中文翻译:
通过选择性硼氢化物还原的Orthoamides Ñ,Ñ ',Ñ “-triacyl-和Ñ,Ñ ',Ñ ” -三(烷氧基羰基)-guanidines
Ñ,Ñ ',Ñ “-Triacylguanidines和Ñ,Ñ ',Ñ ” -三(烷氧基羰基)胍的制备和在四氢呋喃和乙酸的混合物中,用硼氢化盐还原,得到三酰基中的产率和三(烷氧基羰基)orthoamides 40–85%。但是,类似的减少Ñ,Ñ ',Ñ “ -三(吨丁氧基羰基)胍没有给orthoamide但缩醛胺二(吨丁基)亚甲基二。