Choudary, Boyapati M. ; Chowdari, Naidu S. ; Jyothi, Karangula ; Kantam, Mannepalli L. (2002) MCM-41 anchored cinchona alkaloid for catalytic asymmetric dihydroxylation of olefins: a clean protocol for chiral diols using molecular oxygen Catalysis Letters, 82 (1-2). pp. 99-102. ISSN 1011-372X
Full text not available from this repository.
Official URL: http://www.springerlink.com/content/j030t8873548q4...
Related URL: http://dx.doi.org/10.1023/A:1020504511203
Abstract
MCM-41 anchored 1,4-bis(9-O-quininyl)phthalazine (MCM-(QN)2PHAL)-OsO4, is prepared for the first time and used in the heterogeneous asymmetric dihydroxylation of olefins to afford diols with good to excellent enantiomeric excesses in the presence of N-methylmorpholine N-oxide, K3Fe(CN)6 or molecular oxygen as cooxidants.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Springer-Verlag. |
| Keywords: | Asymmetric Synthesis; Dihydroxylation; Immobilization; Olefins; Oxygen; Osmium |
| ID Code: | 6850 |
| Deposited On: | 26 Oct 2010 05:22 |
| Last Modified: | 28 May 2011 09:05 |
Repository Staff Only: item control page
