1.
RSC Adv
; 7(47): 29835-29838, 2017 Jun 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28670448
RESUMO
Our efforts to develop a scalable and divergent synthesis of cyclic di-nucleotide analog precursors have resulted in (1) an orthogonally protected di-amino carbohydrate as well as (2) the novel application of the Staudinger ligation to provide medium-sized macrocycles featuring carbamate or urea linkages.