Asymmetric Rh-Catalyzed Intermolecular Hydroacylation of 1,5-Hexadiene with Salicylaldehyde

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概要

• 論文の詳細を見る

• Asymmetric intermolecular hydroacylation between salicylaldehyde (1) and 1,5-hexadiene (2) using a combination of [RhCl(C8H14)2]2 (0.10 eq), (S)-BINAP (0.10 eq), and ZnBr2 (0.20 eq) afforded an enantiomerically enriched hydroacylated product iso-3 of 84% ee, along with an achiral product normal-3.

• 社団法人 日本薬学会の論文

著者

• 田中 正一

  Graduate School Of Pharmaceutical Sciences Kyushu University

• Imai Masanori

  Graduate School Of Pharmaceutical Sciences Kyushu University

• TANAKA Masakazu

  Graduate School of Pharmaceutical Sciences, Kyushu University

• SUEMUNE Hiroshi

  Graduate School of Pharmaceutical Sciences, Kyushu University

• Tanaka Muneo

  Research Center Shiseido Ltd.

• Tanaka M

  Faculty Of Pharmaceutical Sciences Tokushima Bunri University

• Inui Yasuhiro

  Graduate School of Pharmaceutical Sciences, Kyushu University

• Imai Masanori

  Hokkaido College of Pharmacy

• Tanaka Keitaro

  Graduate School of Pharmaceutical Sciences, Kyushu University

• 田中 誠

  School Of Pharmaceutical Sciences Kitasato University

• Suemune Hiroshi

  Graduate School Of Pharmaceutical Sciences Kyushu University

• Tanaka Masakazu

  Graduate School Of Comprehensive Human Sciences University Of Tsukuba

• Tanaka Masakazu

  Graduate School of Biomedical Sciences, Nagasaki University

• TANAKA Masakazu

  Graduate School of Agriculture, Hokkaido University

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