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Ortho group activation of a bromopyrrole ester in Suzuki-Miyaura cross-coupling reactions: Application to the synthesis of new microtubule depolymerizing agents with potent cytotoxic activities
- Source :
- Bioorganic & Medicinal Chemistry. 25:3206-3214
- Publication Year :
- 2017
- Publisher :
- Elsevier BV, 2017.
-
Abstract
- New microtubule depolymerizing agents with potent cytotoxic activities have been prepared with a 5-cyano or 5-oximino group attached to a pyrrole core. The utilization of ortho activation of a bromopyrrole ester to facilitate successful Suzuki-Miyaura cross-coupling reactions was a key aspect of the synthetic methodology. This strategy allows for control of regiochemistry with the attachment of four completely different groups at the 2, 3, 4 and 5 positions of the pyrrole scaffold. Biological evaluations and molecular modeling studies are reported for these examples.
- Subjects :
- Halogenation
Molecular model
Cell Survival
Stereochemistry
Clinical Biochemistry
Pharmaceutical Science
Antineoplastic Agents
010402 general chemistry
Microtubules
01 natural sciences
Biochemistry
Article
Coupling reaction
chemistry.chemical_compound
Microtubule
Cell Line, Tumor
Neoplasms
Drug Discovery
Animals
Humans
Cytotoxic T cell
Pyrroles
Molecular Biology
Cell Proliferation
Pyrrole
010405 organic chemistry
Organic Chemistry
Regioselectivity
Rats
0104 chemical sciences
Molecular Docking Simulation
chemistry
Molecular Medicine
Cattle
Subjects
Details
- ISSN :
- 09680896
- Volume :
- 25
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....c746da3d09d873926805178613f0d2d1
- Full Text :
- https://doi.org/10.1016/j.bmc.2017.04.012