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Copper-Catalyzed Formal Transfer Hydrogenation/Deuteration of Aryl Alkynes
Author(s) -
Samantha E. Sloane,
Albert Reyes,
Zoua Pa Vang,
Lingzi Li,
Kiera T. Behlow,
Joseph R. Clark
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.0c03632
Subject(s) - chemistry , alkyne , transfer hydrogenation , alkene , catalysis , silanes , regioselectivity , aryl , deuterium , copper , organic chemistry , yield (engineering) , photochemistry , combinatorial chemistry , alkyl , silane , ruthenium , physics , materials science , quantum mechanics , metallurgy
A copper-catalyzed reduction of alkynes to alkanes and deuterated alkanes is described under transfer hydrogenation and transfer deuteration conditions. Commercially available alcohols and silanes are used interchangeably with their deuterated analogues as the hydrogen or deuterium sources. Transfer deuteration of terminal and internal aryl alkynes occurs with high levels of deuterium incorporation. Alkyne-containing complex natural product analogues undergo transfer hydrogenation and transfer deuteration selectively, in high yield. Mechanistic experiments support the reaction occurring through a cis -alkene intermediate and demonstrate the possibility for a regioselective alkyne transfer hydrodeuteration reaction.

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