Erick Martins de Carvalho Pinheiro in research grants and scholarships supported by FAPESP.
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RuCl2(p-cymene)]2 catalyst is the more widely employed ruthenium source in C-H functionalization. Recently, ruthenacycles were reported as efficient catalyst foralkylation and arylation reactions under mild conditions In both cases, catalyticsystems provide non chiral products.Herein, we aim to develop a methodology of enantioselective C-H activationcatalyzed by ruthenium . For this new r…
The functionalization organic molecules through the activation of C-H bonds are among the most common transition metals catalyzed reactions. Despite the large number of examples in enantioselective transformations, there are still no reports on the use of ruthenium as a catalyst. This project aims to develop the first C-H activation reaction for this metal, using new half-sandwich ligands…
Asymmetric transition metal-catalyzed cross-coupling reactions are pivotal C-C bondformingprocesses in organic synthesis. In the PhD currently in progress in Brazil we havesynthesized Ruthenium complexes bearing oxazoline ligands and evaluated theirapplication in C-H arylation and C-H alkylation reactions - using aryl halides, iodoniumsalts and olefins, respectively. In this proposal, we …
| 2 / 2 | Completed scholarships in Brazil |
| 1 / 1 | Ongoing scholarships abroad |
| 3 / 3 | All Scholarships |
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