Title: Hydroboration of Terminal Alkenes and trans‐1,2‐Diboration of Terminal Alkynes Catalyzed by a Manganese(I) Alkyl Complex
Authors: Weber, Stefan 
Zobernig, Daniel Patrick 
Stöger, Berthold  
Veiros, Luis Filipe  
Kirchner, Karl  
Category: Original Research Article
Issue Date: 29-Oct-2021
Citation: 
Weber, S., Zobernig, D. P., Stöger, B., Veiros, L. F., & Kirchner, K. (2021). Hydroboration of Terminal Alkenes and trans‐1,2‐Diboration of Terminal Alkynes Catalyzed by a Manganese(I) Alkyl Complex. Angewandte Chemie, 133(46), 24693–24697. https://doi.org/10.1002/ange.202110736
Journal: Angewandte Chemie 
ISSN: 0044-8249
Abstract: 
A MnI-catalyzed hydroboration of terminal alkenes and a 1,2-diboration of terminal alkynes with pinacolborane (HBPin) is described. For alkenes, anti-Markovnikov hydroboration takes place; for alkynes the reaction proceeds with excellent trans-1,2-selectivity. The most active pre-catalyst is bench-stable alkyl bisphosphine MnI complex fac-[Mn(dippe)(CO)3(CH2CH2CH3)]. The catalytic process is initiated by migratory insertion of a CO ligand into the Mn–alkyl bond to yield an acyl intermediate, which undergoes B−H bond cleavage of HBPin (for alkenes) and rapid C−H bond cleavage (for alkynes), forming the active MnI boryl and acetylide catalysts [Mn(dippe)(CO)2(BPin)] and [Mn(dippe)(CO)2(C≡CR)], respectively. A broad variety of aromatic and aliphatic alkenes and alkynes was efficiently and selectively borylated. Mechanistic insights are provided based on experimental data and DFT calculations revealing that an acceptorless reaction is operating involving dihydrogen release.
Keywords: Manganese
DOI: 10.1002/ange.202110736
Organisation: E163 - Institut für Angewandte Synthesechemie 
License: CC BY 4.0 CC BY 4.0
Publication Type: Article
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