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Asymmetric transfer hydrogenation of ketones using amino alcohol and monotosylated diamine derivatives of indane
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UNSPECIFIED (2002) Asymmetric transfer hydrogenation of ketones using amino alcohol and monotosylated diamine derivatives of indane. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 (3). pp. 416-427. doi:10.1039/b108538g ISSN 1472-7781.
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Official URL: http://dx.doi.org/10.1039/b108538g
Abstract
A series of 1,2-amino alcohol and 1,2-monotosylated diamine derivatives of indane have been applied as ligands in the asymmetric ruthenium(II)-catalysed transfer hydrogenation reaction of a series of ketones. Of these, the cis-1-aminoindan-2-ol derivative gives some of the highest asymmetric inductions reported for any amino alcohol ligand in this application.
Item Type: | Journal Article | ||||
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Subjects: | Q Science > QD Chemistry | ||||
Journal or Publication Title: | JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | ||||
Publisher: | ROYAL SOC CHEMISTRY | ||||
ISSN: | 1472-7781 | ||||
Official Date: | 2002 | ||||
Dates: |
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Number: | 3 | ||||
Number of Pages: | 12 | ||||
Page Range: | pp. 416-427 | ||||
DOI: | 10.1039/b108538g | ||||
Publication Status: | Published |
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