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Co-catalyzed Selective syn-Hydrosilylation of Internal Alkynes

Title data

Stachowiak-Dłużyńska, Hanna ; Kuciński, Krzysztof ; Wyrzykiewicz, Bożena ; Kempe, Rhett ; Hreczycho, Grzegorz:
Co-catalyzed Selective syn-Hydrosilylation of Internal Alkynes.
In: ChemCatChem. Vol. 15 (2023) Issue 14 . - e202300592.
ISSN 1867-3899
DOI: https://doi.org/10.1002/cctc.202300592

Official URL: Volltext

Abstract in another language

Abstract Vinylsilanes are highly appealing and convenient chemical derivatives, as evidenced by the increasing number of synthetic transformations utilizing this class of compounds. Herein, a new comprehensive cobalt-catalyzed procedure has been developed enabling selective hydrosilylation of internal aryl-, alkyl-, and silylalkynes. Cobalt complexes bearing triazine-based PNP pincer-type ligands provide exclusive syn-addition of primary as well as secondary silanes to C≡C bonds. As a result, (E)-silylalkenes and vicinal disilylalkenes were effectively obtained with excellent stereoselectivity and regioselectivity. Unlike several TM-catalyzed procedures, no external additives were required since hydrosilanes act as both substrates and activators.

Further data

Item Type: Article in a journal
Refereed: Yes
Keywords: alkynes; alkynylsilanes; cobalt; hydrosilylation; vinylsilanes
Institutions of the University: Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair Inorganic Chemistry II > Chair Inorganic Chemistry II - Univ.-Prof. Dr. Rhett Kempe
Faculties
Faculties > Faculty of Biology, Chemistry and Earth Sciences
Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry
Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair Inorganic Chemistry II
Result of work at the UBT: Yes
DDC Subjects: 500 Science > 540 Chemistry
Date Deposited: 21 Oct 2023 21:04
Last Modified: 23 Oct 2023 06:55
URI: https://eref.uni-bayreuth.de/id/eprint/87349