Near quantitative synthesis of urea macrocycles enabled by bulky N-substituent
Macrocycles are molecular structures extensively used in the design of catalysts, therapeutics and supramolecular assemblies but synthesis procedures that can produce macrocycles in high yield under high reaction concentrations are rare. Here the authors report the use of dynamic hindered urea bond...
Guardado en:
Autores principales: | Yingfeng Yang, Hanze Ying, Zhixia Li, Jiang Wang, Yingying Chen, Binbin Luo, Danielle L. Gray, Andrew Ferguson, Qian Chen, Y. Z, Jianjun Cheng |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/787290b568cd4e2da9c4a5349f34da43 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Approaching isotropic charge transport of n-type organic semiconductors with bulky substituents
por: Craig P. Yu, et al.
Publicado: (2021) -
Towards the prediction of feed intake capacity of modern broilers on bulky feeds
por: James Taylor, et al.
Publicado: (2021) -
Characterization of a dual function macrocyclase enables design and use of efficient macrocyclization substrates
por: Clarissa M. Czekster, et al.
Publicado: (2017) -
PrimPol-dependent single-stranded gap formation mediates homologous recombination at bulky DNA adducts
por: Ann Liza Piberger, et al.
Publicado: (2020) -
Marine furanocembranoids-inspired macrocycles enabled by Pd-catalyzed unactivated C(sp3)-H olefination mediated by donor/donor carbenes
por: Jiping Hao, et al.
Publicado: (2021)