Empowering alcohols as carbonyl surrogates for Grignard-type reactions
Alcohols are more naturally abundant than carbonyl compounds, which in turn are well known for their reactivity in Grignard reactions. Here, the authors showcase a distinct Grignard-like reactivity by using alcohols as coupling partners with hydrazones and synthesize more complex alcohols under ruth...
Guardado en:
Autores principales: | Chen-Chen Li, Haining Wang, Malcolm M. Sim, Zihang Qiu, Zhang-Pei Chen, Rustam Z. Khaliullin, Chao-Jun Li |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2020
|
Materias: | |
Acceso en línea: | https://doaj.org/article/c45718de9c8b46ddba7d11418ba37090 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
SYNTHESIS OF O-SUBSTITUTED BENZOPHENONES BY GRIGNARD REACTION OF 3-SUBSTITUTED ISOCOUMARINS
por: MANIVEL,P, et al.
Publicado: (2008) -
Christiane Desafy-Grignard. Arthur Miller.
por: Susan Blattès
Publicado: (2006) -
Identification of active catalysts for the acceptorless dehydrogenation of alcohols to carbonyls
por: Tao Wang, et al.
Publicado: (2021) -
Catalytic enantioselective addition of Grignard reagents to aromatic silyl ketimines
por: Jiawei Rong, et al.
Publicado: (2016) -
Comparative analysis of oxidative metabolism indicators at acute alcohol and acute surrogate alcohol intoxication
por: I. V. Beynikova, et al.
Publicado: (2016)