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|Title:||Aldimine-directed branched-selective hydroarylation of styrenes||Authors:||Lee, Pin-Sheng
|Keywords:||DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis||Issue Date:||2013||Source:||Lee, P.-S., & Yoshikai, N. (2013). Aldimine-directed branched-selective hydroarylation of styrenes. Angewandte chemie international edition, 52(4), 1240-1244.||Series/Report no.:||Angewandte chemie international edition||Abstract:||Branching out: A simple and inexpensive cobalt/triarylphosphine catalyst promotes aldimine-directed hydroarylation of styrene with high branched regioselectivity to afford 1,1-diarylethane derivatives in good yields under mild reaction conditions. The ortho-formyl group in the hydroarylation products is amenable to dehydrative cyclization, to give fused polycyclic aromatic hydrocarbons, as well as decarbonylative removal.||URI:||https://hdl.handle.net/10356/98202
|DOI:||10.1002/anie.201207958||Fulltext Permission:||none||Fulltext Availability:||No Fulltext|
|Appears in Collections:||SPMS Journal Articles|
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