Cargando…
Fragmentation of Bicyclic γ-Silyloxy-β-hydroxy-α-diazolactones as an Approach to Ynolides
[Image: see text] Medium-sized ynolides were prepared by the Lewis acid-mediated fragmentation of bicyclic γ-silyloxy-β-hydroxy-α-diazolactones in which the Cβ–Cγ bond is the ring fusion bond. Although these lactone fragmentation substrates reacted somewhat less efficiently than their carbocyclic co...
Autores principales: | Bayir, Ali, Brewer, Matthias |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4084849/ https://www.ncbi.nlm.nih.gov/pubmed/24922068 http://dx.doi.org/10.1021/jo500634d |
Ejemplares similares
-
DFT Studies on the Stereoselectivity of α-Silyloxy Diazoalkane Cycloadditions
por: O’Connor, Matthew J., et al.
Publicado: (2015) -
Synthesis of tetrasubstituted 1-silyloxy-3-aminobutadienes and chemistry beyond Diels–Alder reactions
por: Li, Xijian, et al.
Publicado: (2015) -
Unveiling meta-Alkyloxy/-Silyloxy-Substituted N-Aryl PNP Ligands for Efficient Cr-Catalyzed Ethylene
Tetramerization
por: Barman, Samir, et al.
Publicado: (2023) -
A strategic approach to [6,6]-bicyclic lactones: application towards the CD fragment of DHβE
por: Jepsen, Tue Heesgaard, et al.
Publicado: (2017) -
A New, Convenient Way to Fully Substituted α,β-Unsaturated γ-Hydroxy Butyrolactams
por: Aksenov, Alexander V., et al.
Publicado: (2023)