Please use this identifier to cite or link to this item:
https://hdl.handle.net/2445/53194
Title: | Stereoselective Acetate Aldol Reactions From Metal Enolates |
Author: | Ariza Piquer, Xavier García Gómez, Jordi Romea, Pedro Urpí Tubella, Fèlix |
Keywords: | Reacció aldòlica Productes naturals Quiralitat Catàlisi Aldol reaction Natural products Chirality Catalysis |
Issue Date: | 2011 |
Publisher: | Georg Thieme Verlag |
Abstract: | This review deals with metal enolate-mediated stereoselective acetate aldol reactions. It summarizes recent advances on aldol additions of unsubstituted metal enolates from chiral auxiliaries, stoichiometric and catalytic Lewis acids, or acting in substrate- controlled reactions, which provide stereocontrolled aldol transformations that allow the efficient synthesis of structurally complex natural products. |
Note: | Versió postprint del document publicat a: http://dx.doi.org/10.1055/s-0030-1260040 |
It is part of: | Synthesis. Journal of Synthetic Organic Chemistry, 2011, vol. 2011, num. 14, p. 2175-2191 |
URI: | https://hdl.handle.net/2445/53194 |
Related resource: | http://dx.doi.org/10.1055/s-0030-1260040 |
ISSN: | 0039-7881 |
Appears in Collections: | Articles publicats en revistes (Química Inorgànica i Orgànica) |
Files in This Item:
File | Description | Size | Format | |
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597521.pdf | 615.71 kB | Adobe PDF | View/Open |
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