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Nickel-catalyzed regioselective carbocyclization of ortho-halophenyl ketones with propiolates: An efficient route to disubstituted indenols
Dinesh Kumar Rayabarapu
and
Chien-Hong Cheng
Chemical Communications, (9), pp.942-943
07/05/2002
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Abstract
Carbocylization of o-halophenyl ketones with propiolates in the presence of Ni(dppe)Br
2
and Zn powder in acetonitrile at 80°C afforded the corresponding 2,3-disubstituted indenols.
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Title
Nickel-catalyzed regioselective carbocyclization of ortho-halophenyl ketones with propiolates: An efficient route to disubstituted indenols
Creators - without role
Dinesh Kumar Rayabarapu - Department of Chemistry , Tsing Hua University
Chien-Hong Cheng - Department of Chemistry , Tsing Hua University
Identifiers
9957775213706774
Academic Unit
National Tsing Hua University
Language
English
Resource Type
Journal article
Publication Details
Chemical Communications, (9), pp.942-943
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Nickel-catalyzed_regioselective_carbocyclization_of_ortho-halophenyl_ketones_with_propiolates__an_efficient_route_to_disubstituted_indenols.pdf
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