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Direct Catalytic Asymmetric Enolexo Aldolizations

✍ Scribed by Chandrakala Pidathala; Linh Hoang; Nicola Vignola; Benjamin List

Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
108 KB
Volume
42
Category
Article
ISSN
0044-8249

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πŸ“œ SIMILAR VOLUMES

Direct Catalytic Asymmetric Enolexo Aldo
Direct Catalytic Asymmetric Enolexo Aldolizations
✍ Chandrakala Pidathala; Linh Hoang; Nicola Vignola; Benjamin List πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 107 KB
Direct Catalytic Asymmetric enolexo Aldo
Direct Catalytic Asymmetric enolexo Aldolizations.
✍ Chandrakala Pidathala; Linh Hoang; Nicola Vignola; Benjamin List πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons βš– 121 KB

## Abstract For Abstract see ChemInform Abstract in Full Text.

Titelbild: Direct Catalytic Asymmetric E
Titelbild: Direct Catalytic Asymmetric Enolexo Aldolizations (Angew. Chem. 24/2003)
✍ Chandrakala Pidathala; Linh Hoang; Nicola Vignola; Benjamin List πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 22 KB

**Federleicht katalysiert …︁** die auf dem Titelbild gezeigte AminosΓ€ure (__S__)‐Prolin eine Reihe von asymmetrischen intramolekularen Aldolisierungen, ΓΌber die B. List et al. auf S. 2891 ff. berichten. Die vorgestellten __enolexo__‐Aldolisierungen ergΓ€nzen die in jΓΌngster Zeit rasch wachsende Grupp

The Direct Catalytic Asymmetric Aldol Re
The Direct Catalytic Asymmetric Aldol Reaction
✍ Benito Alcaide; Pedro Almendros πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 174 KB πŸ‘ 2 views

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