Unique effect of coordination of an alkene moiety in products on ruthenium-catalyzed chemoselective C-H alkenylation.
Unique effect of coordination of an alkene moiety in products on ruthenium-catalyzed chemoselective C-H alkenylation.
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DOI:
10.1021/ol802819b
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发表时间:
2009-01
期刊:
影响因子:
5.2
通讯作者:
S. Ueno;Takuya Kochi;N. Chatani;F. Kakiuchi
中科院分区:
文献类型:
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作者:
S. Ueno;Takuya Kochi;N. Chatani;F. Kakiuchi
Ruthenium-catalyzed alkenylation of 2'-alkoxyacetophenones with alkenylboronates provides ortho C-H alkenylation products without sacrificing an ether functional group at the other ortho position. Both excellent chemoselectivity and high product yields are achieved with an aryloxo ruthenium complex. The effective suppression of the C-O bond cleavage was attained by coordination of the alkenyl moiety in the C-H alkenylation product to the ruthenium center.