Triflamides for protection and cyclization of tetraamines to tetraazamacrocycles
摘要:
A facile two-step synthesis of tetraazamacrocycles is reported starting from trifluoromethanesulfonyl derivatives of linear tetraamines. After cyclization, the macrocycle was deprotected using sodium in liquid ammonia.
Triflamides for protection and cyclization of tetraamines to tetraazamacrocycles
摘要:
A facile two-step synthesis of tetraazamacrocycles is reported starting from trifluoromethanesulfonyl derivatives of linear tetraamines. After cyclization, the macrocycle was deprotected using sodium in liquid ammonia.
Triflamides for protection and cyclization of tetraamines to tetraazamacrocycles
作者:V. Panetta、J.J. Yaouanc、H. Handel
DOI:10.1016/s0040-4039(00)61129-2
日期:1992.9
A facile two-step synthesis of tetraazamacrocycles is reported starting from trifluoromethanesulfonyl derivatives of linear tetraamines. After cyclization, the macrocycle was deprotected using sodium in liquid ammonia.