Cargando…
Synthesis of skeletally diverse alkaloid-like molecules: exploitation of metathesis substrates assembled from triplets of building blocks
A range of metathesis substrates was assembled from triplets of unsaturated building blocks. The approach involved the iterative attachment of a propagating and a terminating building block to a fluorous-tagged initiating building block. Metathesis cascade chemistry was used to “reprogram” the molec...
Autores principales: | Maurya, Sushil K, Dow, Mark, Warriner, Stuart, Nelson, Adam |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678641/ https://www.ncbi.nlm.nih.gov/pubmed/23766790 http://dx.doi.org/10.3762/bjoc.9.88 |
Ejemplares similares
-
An eco-compatible strategy for the diversity-oriented synthesis of macrocycles exploiting carbohydrate-derived building blocks
por: Maurya, Sushil K, et al.
Publicado: (2017) -
Cross metathesis of unsaturated epoxides for the synthesis of polyfunctional building blocks
por: Abderrezak, Meriem K, et al.
Publicado: (2015) -
An efficient method for synthesising unsymmetrical silaketals: substrates for ring-closing, including macrocycle-closing, metathesis
por: Cordier, Christopher, et al.
Publicado: (2008) -
Profluorescent substrates for the screening of olefin metathesis catalysts
por: Reuter, Raphael, et al.
Publicado: (2015) -
Bidirectional cross metathesis and ring-closing metathesis/ring opening of a C(2)-symmetric building block: a strategy for the synthesis of decanolide natural products
por: Schmidt, Bernd, et al.
Publicado: (2013)