Highly Selective Addition of Chiral, Sulfonimidoyl Substituted Bis(allyl)titanium Complexes to N-Sulfonyl α-Imino Esters: Asymmetric Synthesis of γ,δ-Unsaturated α-Amino Acids Bearing a Chiral, Electron-Withdrawing Nucleofuge at the δ-Position-Reference-Cited by-同舟云学术

Highly Selective Addition of Chiral, Sulfonimidoyl Substituted Bis(allyl)titanium Complexes to N-Sulfonyl α-Imino Esters: Asymmetric Synthesis of γ,δ-Unsaturated α-Amino Acids Bearing a Chiral, Electron-Withdrawing Nucleofuge at the δ-Position

Published:2002-06-07 Issue:26 Volume:124 Page:7789-7800
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Schleusner Marcel¹,Gais Hans-Joachim¹,Koep Stefan¹,Raabe Gerhard¹

Affiliation:

1. Contribution from the Institut für Organische Chemie der Rheinisch-Westfälischen Technischen Hochschule (RWTH) Aachen, Professor-Pirlet-Strasse 1, D-52056 Aachen, Germany

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0201799

Reference123 articles.

1. Highly Regio- and Enantioselective Catalytic Hydrogenation of Enamides in Conjugated Diene Systems: Synthesis and Application of γ,δ-Unsaturated Amino Acids

2. Catalytic asymmetric hydrogenation of β-substituted α,β,γ,δ-unsaturated amino acids

3. CC-Verknüpfung von Carbonsäuren mit Allylalkoholen unter Verwendung von 2-Phenylglycin als Vehikel

4. Ester-enolate Claisen rearrangement of .alpha.-amino acid derivatives

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