746670-85-9Relevant academic research and scientific papers
Enantioselective synthesis of benzyl (1S,2R,4R)-4-(tert- butoxycarbonylamino)-2-(hydroxymethyl)-cyclohexylcarbamate using an iodolactamization as the key step
Campbell, Carlton L.,Hassler, Carla,Ko, Soo S.,Voss, Matthew E.,Guaciaro, Michael A.,Carter, Percy H.,Cherney, Robert J.
supporting information; experimental part, p. 6368 - 6370 (2009/12/08)
(Chemical Equation Presented) An efficient enantioselective synthesis of benzyl (1S,2R,4R)-4-(tert-butoxycarbonylamino)-2-(hydroxymethyl) cyclohexylcarbamate 2, an essential intermediate for a series of potent CCR2 antagonists, is described. The key step
