EventsMOL2NET'17, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 3rd ed.
Published
This submission belongs to the session 01. CHEMBIOINFO-03: Chem-Bioinformatics Congress Cambridge, UK-Chapel Hill and Richmond, USA, 2017 of the event MOL2NET'17, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 3rd ed.
Published date
19 Dec, 2017
Citation
Esther Domínguez, Garazi Urgoitia, María Teresa Herrero, Raul Sanmartin, Diyne formation from alkynes in the presence of palladium pincer complexes, in Proceedings of MOL2NET'17, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 3rd ed., 15 January–15 December 2017, MDPI: Basel, Switzerland, doi: 10.3390/mol2net-03-05090
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Diyne formation from alkynes in the presence of palladium pincer complexes

Esther Domínguez 1
Garazi Urgoitia 1
María Teresa Herrero 1
Raul Sanmartin 1
1. University of Basque Country
Abstract

1,3-Diynes are valuable building blocks for biologically active molecules and precursors of polymers, macrocycles and supramolecular structures. The combination of metal catalysts and molecular oxygen is considered a suitable protocol for the direct homocoupling of alkynes leading to diynes. Regarding the catalyst, palladium species have proved to be efficient and selective, but copper salts as co-catalysts and/or stoichiometric amounts of reoxidants are often needed. Palladium pincer complexes are presented as alternative palladium sources for the homocoupling of alkynes in an environmentally friendly solvent as polyethylene glycol, in the absence of any other co-catalyst and under aerobic conditions

Keywords
alkyne homocoupling
diyne
palladium
pincer
aerobic
Poster
mol2net-03_ homocoupling.pdf
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