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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. 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 |
|---|---|
| Subjects: | Q Science > QD Chemistry |
| Journal or Publication Title: | JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 |
| Publisher: | ROYAL SOC CHEMISTRY |
| ISSN: | 1472-7781 |
| Date: | 2002 |
| Number: | 3 |
| Number of Pages: | 12 |
| Page Range: | pp. 416-427 |
| Identification Number: | 10.1039/b108538g |
| Publication Status: | Published |
| URI: | http://wrap.warwick.ac.uk/id/eprint/11301 |
Data sourced from Thomson Reuters' Web of Knowledge
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