Refinement of the Catalyst Backbone of Chiral Intramolecular Silicon-Sulfur Lewis Pairs: Improved Enantioselectivity in the Diels-Alder Reaction of Cyclohexa-1,3-diene and Chalcone Derivatives-Reference-Cited by-同舟云学术

Refinement of the Catalyst Backbone of Chiral Intramolecular Silicon-Sulfur Lewis Pairs: Improved Enantioselectivity in the Diels-Alder Reaction of Cyclohexa-1,3-diene and Chalcone Derivatives

Published:2018-05-03 Issue:23 Volume:2018 Page:2896-2901
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Shaykhutdinova Polina¹^ORCID,Kemper Sebastian¹^ORCID,Oestreich Martin¹^ORCID

Affiliation:

1. Institut für Chemie; Technische Universität Berlin; Strasse des 17. Juni 115 10623 Berlin Germany

Funder

Deutsche Forschungsgemeinschaft

Einstein Foundation Berlin

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201800434/fullpdf

Reference32 articles.

1. Intramolecularly Sulfur-Stabilized Silicon Cations as Lewis Acid Catalysts

2. Tris(trimethylsilyl)sulfonium and Methylbis(trimethylsilyl)sulfonium Ions: Preparation, NMR Spectroscopy, and Theoretical Studies1

3. Stabilization of Organosilicenium Ions by means of Intramolecular Coordination of O, S, or P Ligands

4. Stabilisierung von Organosilicenium-Ionen durch intramolekulare Koordination von O-, S- oder P-Liganden

5. Intramolecularly Sulfur-Stabilized Silicon Cations with Chiral Binaphthyl Backbones: Synthesis of Three Different Motifs and Their Application in Enantioselective Diels–Alder Reactions

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