Chemoselective Hydrogenation of Alkynes to (Z)-Alkenes Using an Air-Stable Base Metal Catalyst
Author(s) -
Viktoriia Zubar,
Jan Sklyaruk,
Aleksandra Brzozowska,
Magnus Rueping
Publication year - 2020
Publication title -
organic letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.94
H-Index - 239
eISSN - 1523-7060
pISSN - 1523-7052
DOI - 10.1021/acs.orglett.0c01783
Subject(s) - chemistry , bifunctional , catalysis , allylic rearrangement , manganese , ligand (biochemistry) , base (topology) , metal , cooperativity , reaction conditions , base metal , alkene , combinatorial chemistry , organic chemistry , mathematical analysis , biochemistry , materials science , receptor , mathematics , welding , metallurgy
A highly selective hydrogenation of alkynes using an air-stable and readily available manganese catalyst has been achieved. The reaction proceeds under mild reaction conditions and tolerates various functional groups, resulting in ( Z )-alkenes and allylic alcohols in high yields. Mechanistic experiments suggest that the reaction proceeds via a bifunctional activation involving metal-ligand cooperativity.
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