Cargando…
Crossed Regio‐ and Enantioselective Iron‐Catalyzed [4+2]‐Cycloadditions of Unactivated Dienes
The cyclohexene motif is ubiquitous in nature and specialty chemicals. A straightforward selective access to chiral cyclohexenes from unactivated dienes and dienophiles is not feasible by classical Diels–Alder reaction and constitutes an unsolved synthetic challenge. We report a mild and enantiosele...
Autores principales: | Braconi, Elena, Cramer, Nicolai |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299977/ https://www.ncbi.nlm.nih.gov/pubmed/34708502 http://dx.doi.org/10.1002/anie.202112148 |
Ejemplares similares
-
Chemodivergent, Regio‐ and Enantioselective Cycloaddition Reactions between 1,3‐Dienes and Alkynes
por: Singh, Dipshi, et al.
Publicado: (2023) -
Directed nickel-catalyzed regio- and diastereoselective arylamination of unactivated alkenes
por: Xie, Leipeng, et al.
Publicado: (2021) -
Silicon-oriented regio- and enantioselective rhodium-catalyzed hydroformylation
por: You, Cai, et al.
Publicado: (2018) -
Nickel/Brønsted acid dual-catalyzed regio- and enantioselective hydrophosphinylation of 1,3-dienes: access to chiral allylic phosphine oxides
por: Long, Jiao, et al.
Publicado: (2021) -
Regio- and Enantioselective Catalytic Monoepoxidation
of Conjugated Dienes: Synthesis of Chiral Allylic cis-Epoxides
por: Jat, Jawahar L., et al.
Publicado: (2015)