Kunhua Lin

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Name: 林昆华; Lin, KunHua
Organization: Shanghai University , China
Department: Department of Chemistry
Title: Associate Professor(PhD)
Co-reporter:Zhuye Liang, Weichao Xue, Kunhua Lin, and Hegui Gong
Organic Letters 2014 Volume 16(Issue 21) pp:5620-5623
Publication Date(Web):October 21, 2014
DOI:10.1021/ol502682q
Methylation of unactivated alkyl halides and acid chlorides under Ni-catalyzed reductive coupling conditions led to efficient formation of methylated alkanes and ketones using methyl p-methyl tosylate as the methylation reagent. Moderate to excellent coupling yields as well as excellent functional group tolerance were observed under the present mild and easy-to-operate reaction conditions.
BENZENE, 1-CHLORO-4-[(1E)-2-CYCLOPENTYLETHENYL]-
Naphthalene, 2-[(1E)-2-bromoethenyl]-
Naphthalene, 2-(2,2-dibromoethenyl)-
Benzene, [(1E,3E)-4-bromo-1,3-butadienyl]-
Benzene, 1-(2,2-dibromoethenyl)-4-fluoro-
Benzene, (4,4-dibromo-3-butenyl)-
Benzene, 1-[(1E)-2-bromoethenyl]-4-fluoro-
Benzene, [(1E)-4,4-dibromo-1,3-butadienyl]-