Cargando…
A diversity-oriented synthesis of bioactive benzanilides via a regioselective C(sp(2))–H hydroxylation strategy
A diversity-oriented synthesis of bioactive benzanilides via C(sp(2))–H hydroxylation has been studied. Different regioselectivity was observed with Ru(ii) and Pd(ii) catalysts. The reaction demonstrates excellent regioselectivity, good tolerance of functional groups, and high yields. A wide range o...
Autores principales: | Sun, Yong-Hui, Sun, Tian-Yu, Wu, Yun-Dong, Zhang, Xinhao, Rao, Yu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5975941/ https://www.ncbi.nlm.nih.gov/pubmed/29910911 http://dx.doi.org/10.1039/c5sc03905c |
Ejemplares similares
-
Monooxygenase-catalyzed regioselective hydroxylation for the synthesis of hydroxyequols
por: Hashimoto, Takafumi, et al.
Publicado: (2019) -
Proximity Effects in Mass Spectra of Benzanilides
por: Fenwick, Nathan W, et al.
Publicado: (2021) -
Regioselective Hydroxylation of Phloretin, a Bioactive Compound from Apples, by Human Cytochrome P450 Enzymes
por: Nguyen, Ngoc Anh, et al.
Publicado: (2020) -
Triarylmethanes and their Medium‐Ring Analogues by Unactivated Truce–Smiles Rearrangement of Benzanilides
por: Abrams, Roman, et al.
Publicado: (2021) -
Expanding the scope of native chemical ligation – templated small molecule drug synthesis via benzanilide formation
por: Houska, Richard, et al.
Publicado: (2021)