Scope and limitations of the dual-gold-catalysed hydrophenoxylation of alkynes
Due to the synthetic advantages presented by the dual-gold-catalysed hydrophenoxylation of alkynes, a thorough study of this reaction was carried out in order to fully define the scope and limitations of the methodology. The protocol tolerates a wide range of functional groups, such as nitriles, ket...
Main Authors: | Adrián Gómez-Suárez, Yoshihiro Oonishi, Anthony R. Martin, Steven P. Nolan |
---|---|
Format: | Article |
Language: | English |
Published: |
Beilstein-Institut
2016-02-01
|
Series: | Beilstein Journal of Organic Chemistry |
Subjects: | |
Online Access: | https://doi.org/10.3762/bjoc.12.19 |
Similar Items
-
Acid, silver, and solvent-free gold-catalyzed hydrophenoxylation of internal alkynes
by: Marcia E. Richard, et al.
Published: (2013-10-01) -
Towards Dual-Metal Catalyzed Hydroalkoxylation of Alkynes
by: Oscar F. González-Belman, et al.
Published: (2021-06-01) -
Synthesis, characterization and luminescence studies of gold(I)–NHC amide complexes
by: Adrián Gómez-Suárez, et al.
Published: (2013-10-01) -
Influence of bulky yet flexible N-heterocyclic carbene ligands in gold catalysis
by: Alba Collado, et al.
Published: (2015-10-01) -
Ambient gold-catalyzed O-vinylation of cyclic 1,3-diketone: A vinyl ether synthesis
by: Yumeng Xi, et al.
Published: (2013-11-01)