Cargando…
Hypervalent Iodine-Mediated Diastereoselective α-Acetoxylation of Cyclic Ketones
A binary hybrid system comprising a hypervalent iodine(III) reagent and BF(3)•OEt(2) Lewis acid was found to be effective for the diastereoselective α-acetoxylation of cyclic ketones. In this hybrid system, BF(3)•OEt(2) Lewis acid allowed the activation of the hypervalent iodine(III) reagent and cyc...
Autores principales: | Tan, Jiashen, Zhu, Weiqin, Xu, Weiping, Jing, Yaru, Ke, Zhuofeng, Liu, Yan, Maruoka, Keiji |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7365914/ https://www.ncbi.nlm.nih.gov/pubmed/32754572 http://dx.doi.org/10.3389/fchem.2020.00467 |
Ejemplares similares
-
Hypervalent Iodine(III)‐Catalysed Enantioselective α‐Acetoxylation of Ketones
por: Hokamp, Tobias, et al.
Publicado: (2020) -
Hypervalent iodine(III)-mediated decarboxylative acetoxylation at tertiary and benzylic carbon centers
por: Kiyokawa, Kensuke, et al.
Publicado: (2018) -
Hypervalent iodine(III)-induced methylene acetoxylation of 3-oxo-N-substituted butanamides
por: Liu, Wei-Bing, et al.
Publicado: (2011) -
Mechanism-Dependent Selectivity: Fluorocyclization of Unsaturated Carboxylic Acids or Alcohols by Hypervalent Iodine
por: Su, Jiaqi, et al.
Publicado: (2022) -
Hypervalent Iodine (III) Catalyzed Regio- and Diastereoselective Aminochlorination of Tailored Electron Deficient Olefins via GAP Chemistry
por: Rahman, Anis Ur, et al.
Publicado: (2020)