Abstract
The enantioselectivity of the titanium (IV)-BINOL catalyzed asymmetric Mannich-type reactions of nitrones can be enhanced by using additional chiral ligands. The best results are obtained with diols derived from D-mannitol.
Keywords: nitrones, hydroxylamines, aminoacids, mannich reaction
Letters in Organic Chemistry
Title: Effect of Additional Chiral Ligands in Catalytic Enantioselective Addition of Ketene Silyl Acetals to Nitrones
Volume: 2 Issue: 4
Author(s): P. Merino, S. Franco, P. Jimenez, T. Tejero and M. A. Chiacchio
Affiliation:
Keywords: nitrones, hydroxylamines, aminoacids, mannich reaction
Abstract: The enantioselectivity of the titanium (IV)-BINOL catalyzed asymmetric Mannich-type reactions of nitrones can be enhanced by using additional chiral ligands. The best results are obtained with diols derived from D-mannitol.
Export Options
About this article
Cite this article as:
Merino P., Franco S., Jimenez P., Tejero T. and Chiacchio A. M., Effect of Additional Chiral Ligands in Catalytic Enantioselective Addition of Ketene Silyl Acetals to Nitrones, Letters in Organic Chemistry 2005; 2 (4) . https://dx.doi.org/10.2174/1570178054038803
DOI https://dx.doi.org/10.2174/1570178054038803 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers