Cargando…
1H-Imidazol-4(5H)-ones and thiazol-4(5H)-ones as emerging pronucleophiles in asymmetric catalysis
Asymmetric catalysis represents a very powerful tool for the synthesis of enantiopure compounds. In this context the main focus has been directed not only to the search for new efficient chiral catalysts, but also to the development of efficient pronucleophiles. This review highlights the utility an...
Autores principales: | Mielgo, Antonia, Palomo, Claudio |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902076/ https://www.ncbi.nlm.nih.gov/pubmed/27340482 http://dx.doi.org/10.3762/bjoc.12.90 |
Ejemplares similares
-
Asymmetric [4 + 2] annulation of 5H-thiazol-4-ones with a chiral dipeptide-based Brønsted base catalyst
por: Zhu, Bo, et al.
Publicado: (2016) -
Highly enantioselective construction of tertiary thioethers and alcohols via phosphine-catalyzed asymmetric γ-addition reactions of 5H-thiazol-4-ones and 5H-oxazol-4-ones: scope and mechanistic understandings
por: Wang, Tianli, et al.
Publicado: (2015) -
2-Amino-1-methyl-1H-imidazol-4(5H)-one dimethyl sulfoxide monosolvate
por: Tutughamiarso, Maya, et al.
Publicado: (2010) -
Highly chemo-, enantio-, and diastereoselective [4 + 2] cycloaddition of 5H-thiazol-4-ones with N-itaconimides
por: Qiu, Shuai, et al.
Publicado: (2016) -
(Z)-4-(2-Hydroxybenzylidene)-1-methyl-2-phenyl-1H-imidazol-5(4H)-one
por: Chang, Ming-Jen, et al.
Publicado: (2012)