Direct Catalytic Asymmetric enolexo Aldolizations.
β Scribed by Chandrakala Pidathala; Linh Hoang; Nicola Vignola; Benjamin List
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 121 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
For Abstract see ChemInform Abstract in Full Text.
π SIMILAR VOLUMES
**Federleicht katalysiert β¦οΈ** die auf dem Titelbild gezeigte AminosΓ€ure (__S__)βProlin eine Reihe von asymmetrischen intramolekularen Aldolisierungen, ΓΌber die B. List et al. auf S. 2891 ff. berichten. Die vorgestellten __enolexo__βAldolisierungen ergΓ€nzen die in jΓΌngster Zeit rasch wachsende Grupp
In the synthesis of complex molecular targets, the ability to control the stereoselectivity of the aldol reaction has raised this process to a level of prominence shared by few reactions. In most cases, however, the stoichiometric transformation of the active methylene partner into its enolate or an