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NHC‐Au‐Catalyzed Isomerization of Propargylic B(MIDA)s to Allenes and Double Isomerization of Alkynes to 1,3‐Dienes
https://orcid.org/0000-0002-9648-6759
AbstractThe synthesis of allenyl boronates is an important yet challenging topic in organic synthesis. Reported herein is an NHC‐gold‐catalyzed 1,3‐H shift toward allenyl boronates synthesis from simple propargylic B(MIDA)s. Mechanistic studies suggest dual roles of the boryl moiety in the reaction: to activate the substrate for isomerization and at the same time, to prevent the allene product from further isomerization. These effects should be a result of α‐anion stabilization and α‐cation destabilization conferred by the B(MIDA) moiety, respectively. The NHC‐Au catalyst, which is commercially available, is also found to be reactive in alkyne‐to‐1,3‐diene isomerization reactions in an atom‐economic and base‐free manner.
NHC‐Au‐Catalyzed Isomerization of Propargylic B(MIDA)s to Allenes and Double Isomerization of Alkynes to 1,3‐Dienes
https://orcid.org/0000-0002-9648-6759
AbstractThe synthesis of allenyl boronates is an important yet challenging topic in organic synthesis. Reported herein is an NHC‐gold‐catalyzed 1,3‐H shift toward allenyl boronates synthesis from simple propargylic B(MIDA)s. Mechanistic studies suggest dual roles of the boryl moiety in the reaction: to activate the substrate for isomerization and at the same time, to prevent the allene product from further isomerization. These effects should be a result of α‐anion stabilization and α‐cation destabilization conferred by the B(MIDA) moiety, respectively. The NHC‐Au catalyst, which is commercially available, is also found to be reactive in alkyne‐to‐1,3‐diene isomerization reactions in an atom‐economic and base‐free manner.
NHC‐Au‐Catalyzed Isomerization of Propargylic B(MIDA)s to Allenes and Double Isomerization of Alkynes to 1,3‐Dienes
https://orcid.org/0000-0002-9648-6759
AbstractThe synthesis of allenyl boronates is an important yet challenging topic in organic synthesis. Reported herein is an NHC‐gold‐catalyzed 1,3‐H shift toward allenyl boronates synthesis from simple propargylic B(MIDA)s. Mechanistic studies suggest dual roles of the boryl moiety in the reaction: to activate the substrate for isomerization and at the same time, to prevent the allene product from further isomerization. These effects should be a result of α‐anion stabilization and α‐cation destabilization conferred by the B(MIDA) moiety, respectively. The NHC‐Au catalyst, which is commercially available, is also found to be reactive in alkyne‐to‐1,3‐diene isomerization reactions in an atom‐economic and base‐free manner.
NHC‐Au‐Catalyzed Isomerization of Propargylic B(MIDA)s to Allenes and Double Isomerization of Alkynes to 1,3‐Dienes
Advanced Science
Liu, Li‐Cai (Autor:in) / Lin, Shuang (Autor:in) / Xu, Kangwei (Autor:in) / Qian, Jiasheng (Autor:in) / Wu, Ruibo (Autor:in) / Li, Qingjiang (Autor:in) / Wang, Honggen (Autor:in)
Advanced Science ; 11
01.06.2024
Aufsatz (Zeitschrift)
Elektronische Ressource
Englisch
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