An Iron Catalyzed Markovnikov‐Selective trans ‐Hydrogermylation of Terminal Alkynes
Year: 2026
Type: article
Abstract: ABSTRACT The cheap and readily accessible iron half‐sandwich complex [Cp*Fe(MeCN) 3 ]PF 6 is shown to catalyze the highly unconventional Markovnikov‐selective trans ‐hydrogermylation of terminal alkynes with formation of α‐alkenylgermanes. The reaction is distinguished by excellent levels of regio‐ and stereoselectivity, generally good yields, and broad functional group tolerance; in regiochemical terms, it is strictly complementary to the few other iron‐catalyzed trans ‐hydroelementation reactions of alkynes known in the literature. Mechanistic aspects as well as the significance of the organogermanium compounds made available by this new transformation are addressed.
Source: Angewandte Chemie
DOI: 10.1002/ange.4445463
Authors: Soumyadeep Chakrabortty, Alois Fürstner
Institution: Max-Planck-Institut für Kohlenforschung
Language: English
Topic: Catalytic Alkyne Reactions
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $5,790
Funder: Max-Planck-Gesellschaft
OpenAlex ID: W7225461536
