Substrate-Controlled Product Divergence: Silver-Catalyzed Reaction of Trifluoromethyl Ketones with Terminal Alkynes
Author(s) -
FangLing Li,
Lei Wang,
Cuihua Li,
Ning Liu,
Bin Dai
Publication year - 2017
Publication title -
acs omega
Language(s) - English
Resource type - Journals
ISSN - 2470-1343
DOI - 10.1021/acsomega.6b00432
Subject(s) - terminal (telecommunication) , trifluoromethyl , alkynylation , stereoselectivity , chemistry , yield (engineering) , substrate (aquarium) , aryl , alkyne , catalysis , domino , alkyl , medicinal chemistry , combinatorial chemistry , organic chemistry , materials science , biology , telecommunications , computer science , metallurgy , ecology
A distinct dichotomy in product distribution was initially observed in the silver-catalyzed reaction of trifluoromethyl (CF 3 ) ketones with terminal alkynes having two different types of electronic natures. The domino reaction smoothly proceeded almost exclusively with high stereoselectivity with terminal alkynes containing ester groups, whereas alkynylation occurred in good yield when terminal alkynes containing aryl or alkyl groups were present. The results indicated that the electronic nature of terminal alkynes can act as a switch that enables either the domino reaction or alkynylation between terminal alkynes and CF 3 ketones.
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