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Volumn 3, Issue 8-9, 2008, Pages 1374-1383

Asymmetric transfer hydrogenation of C=O and C=N bonds by tethered Rh III catalysts

Author keywords

Asymmetric catalysis; Hydrogenation; Imines; Ketones; Reduction

Indexed keywords


EID: 54849442488     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.200800189     Document Type: Article
Times cited : (79)

References (106)
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    • Although all the catalysts in this paper can be prepared in either enantiomerically pure form, we have used the (R,R)-diamine ligands throughout this work for simplicity
    • Although all the catalysts in this paper can be prepared in either enantiomerically pure form, we have used the (R,R)-diamine ligands throughout this work for simplicity.
  • 94
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    • II catalyst (R,R)-4 gave a product of 80% ee (S). Dr C. X. Lin performed this reduction.
    • II catalyst (R,R)-4 gave a product of 80% ee (S). Dr C. X. Lin performed this reduction.
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    • Attempts to prepare a catalyst with the methoxy group at the position ortho to the cyclopentadienyl group through direct lithiation of the acetal group of 3-methoxybenzaldehyde were unsuccessful.
    • Attempts to prepare a catalyst with the methoxy group at the position ortho to the cyclopentadienyl group through direct lithiation of the acetal group of 3-methoxybenzaldehyde were unsuccessful.
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    • C. Fruit, P. Mucombining double acute accentller, Helv. Chim. Acta 2004, 87, 1607-1615.
    • C. Fruit, P. Mucombining double acute accentller, Helv. Chim. Acta 2004, 87, 1607-1615.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.