Cargando…
Turning Cucurbit[8]uril into a Supramolecular Nanoreactor for Asymmetric Catalysis
Chiral macromolecules have been widely used as synthetic pockets to mimic natural enzymes and promote asymmetric reactions. An achiral host, cucurbit[8]uril (CB[8]), was used for an asymmetric Lewis acid catalyzed Diels–Alder reaction. We achieved a remarkable increase in enantioselectivity and a la...
Autores principales: | Zheng, Lifei, Sonzini, Silvia, Ambarwati, Masyitha, Rosta, Edina, Scherman, Oren A, Herrmann, Andreas |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643185/ https://www.ncbi.nlm.nih.gov/pubmed/26383272 http://dx.doi.org/10.1002/anie.201505628 |
Ejemplares similares
-
Turning Cucurbit[8]uril into a Supramolecular Nanoreactor for Asymmetric Catalysis
por: Zheng, Lifei, et al.
Publicado: (2015) -
Controlling the structure and photophysics of fluorophore dimers using multiple cucurbit[8]uril clampings
por: Wu, Guanglu, et al.
Publicado: (2019) -
Cucurbit[8]uril directed stimuli-responsive supramolecular polymer brushes for dynamic surface engineering
por: Hu, Chi, et al.
Publicado: (2015) -
Emerging
Two-Dimensional Crystallization of Cucurbit[8]uril
Complexes: From Supramolecular Polymers to Nanofibers
por: Barrio, Jesús del, et al.
Publicado: (2019) -
Supramolecular hydrogel microcapsules via cucurbit[8]uril host–guest interactions with triggered and UV-controlled molecular permeability
por: Yu, Ziyi, et al.
Publicado: (2015)