Synthesis of Optically Active Organoantimony Compounds Having an (S)-α-Methylbenzyldimethylamine Group and Its Evaluation for Asymmetric Reaction
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概要
- 論文の詳細を見る
Novel, enantiomerically pure organoantimony compounds having a C-chiral amine moiety, (S)-(α-methyl-2-di-p-tolylstibanobenzyl)dimethylamine [AMSb] (2) and its (η^6-arene)chromium complex [AMSb-Cr(CO)_3] (4), were prepared from common (S)-(α-methylbenzyl)dimethylamine (1) via its ortho-lithiated intermediates in short steps. The catalytic activity and enantioselectivity of the ligands 2 and 4 for asymmetric reaction are evaluated, and the optically active (η^6-arene)chromium complex 4 has been shown to be an effective ligand for rhodium-catalyzed asymmetric hydrosilylation of ketones.
- 公益社団法人日本薬学会の論文
- 2002-10-01
著者
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KURITA Jyoji
Faculty of Pharmaceutical Sciences, Hokuriku University
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YASUIKE Shuji
Faculty of Pharmaceutical Sciences, Hokuriku University
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Kurita J
Faculty Of Pharmaceutical Sciences Hokuriku University
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Kurita Jyoji
Faculty Of Pharmaceutical Sciences Hokuriku University
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Yasuike S
Faculty Of Pharmaceutical Sciences Hokuriku University
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Okajima S
Faculty Of Pharmaceutical Sciences Hokuriku University
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Yasuike Shuji
Faculty Of Pharmaceutical Sciences Hokuriku University
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OKAJIMA Satoru
Faculty of Pharmaceutical Sciences, Hokuriku University
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- Synthesis of Optically Active Organoantimony Compounds Having an (S)-α-Methylbenzyldimethylamine Group and Its Evaluation for Asymmetric Reaction
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