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The asymmetric ester enolate Claisen rearrangement as a suitable method for the synthesis of sterically highly demanding amino acids

โœ Scribed by Achim Krebs; Uli Kazmaier

Publisher
Elsevier Science
Year
1996
Tongue
French
Weight
168 KB
Volume
37
Category
Article
ISSN
0040-4039

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๐Ÿ“œ SIMILAR VOLUMES

ChemInform Abstract: Asymmetric Ester En
ChemInform Abstract: Asymmetric Ester Enolate Claisen Rearrangement as a Suitable Method for the Synthesis of Sterically Highly Demanding Amino Acids.
โœ A. KREBS; U. KAZMAIER ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 33 KB ๐Ÿ‘ 2 views

Asymmetric Ester Enolate Claisen Rearrangement as a Suitable Method for the Synthesis of Sterically Highly Demanding Amino Acids. -The highly diastereo-and enantioselective synthesis of otherwise difficult to obtain ฮณ,ฮด-unsaturated amino acids containing ฮฒ-quaternary carbon centers (cf. (III), (V);