Development of a new methodology for the preparation of optically active alcohols
Gespeichert in:
Verfasser / Beitragende:
[P. G. Andersson]
Ort, Verlag, Jahr:
2004
Enthalten in:
Pure and Applied Chemistry, 76/3(2004-01-01), 547-555
Format:
Artikel (online)
Online Zugang:
| LEADER | caa a22 4500 | ||
|---|---|---|---|
| 001 | 378923099 | ||
| 003 | CHVBK | ||
| 005 | 20180305123610.0 | ||
| 007 | cr unu---uuuuu | ||
| 008 | 161128e20040101xx s 000 0 eng | ||
| 024 | 7 | 0 | |a 10.1351/pac200476030547 |2 doi |
| 035 | |a (NATIONALLICENCE)gruyter-10.1351/pac200476030547 | ||
| 100 | 1 | |a Andersson |D P. G. |u Department of Organic Chemistry, Uppsala University, Box 599, S-751 24 Uppsala, Sweden | |
| 245 | 1 | 0 | |a Development of a new methodology for the preparation of optically active alcohols |h [Elektronische Daten] |c [P. G. Andersson] |
| 520 | 3 | |a This article summarizes our recent achievements in the asymmetric catalytic formation of chiral alcohols using 3-substituted, 2-azanorbornyl-based ligands. The use of this structural unit in ligand synthesis offers several advantages over the analogous proline chemistry, such as equal availability of both enantiomers and increased rigidity of the catalysts. This ligand has been found to be very useful for the two reactions described in this paper: the ruthenium-catalyzed transfer hydrogenation of ketones, and the base-mediated rearrangement of epoxides. | |
| 540 | |a © 2013 Walter de Gruyter GmbH, Berlin/Boston | ||
| 773 | 0 | |t Pure and Applied Chemistry |d De Gruyter |g 76/3(2004-01-01), 547-555 |x 0033-4545 |q 76:3<547 |1 2004 |2 76 |o pac | |
| 856 | 4 | 0 | |u https://doi.org/10.1351/pac200476030547 |q text/html |z Onlinezugriff via DOI |
| 908 | |D 1 |a research article |2 jats | ||
| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1351/pac200476030547 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 100 |E 1- |a Andersson |D P. G. |u Department of Organic Chemistry, Uppsala University, Box 599, S-751 24 Uppsala, Sweden | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Pure and Applied Chemistry |d De Gruyter |g 76/3(2004-01-01), 547-555 |x 0033-4545 |q 76:3<547 |1 2004 |2 76 |o pac | ||
| 900 | 7 | |b CC0 |u http://creativecommons.org/publicdomain/zero/1.0 |2 nationallicence | |
| 898 | |a BK010053 |b XK010053 |c XK010000 | ||
| 949 | |B NATIONALLICENCE |F NATIONALLICENCE |b NL-gruyter | ||