Lewis acid-catalyzed Friedel–Crafts reactions toward highly versatile, α-quaternary oxime ethers-Reference-Cited by-同舟云学术

Lewis acid-catalyzed Friedel–Crafts reactions toward highly versatile, α-quaternary oxime ethers

Published:2018 Issue:79 Volume:54 Page:11124-11127
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Schlegel Marcel¹²³⁴^ORCID,Schneider Christoph¹²³⁴^ORCID

Affiliation:

1. Institut für Organische Chemie

2. Universität Leipzig

3. D-04103 Leipzig

4. Germany

Abstract

Tertiary 2-hydroxy oxime ethers are converted into α-functionalized, all-carbon-substituted products under Lewis acid catalysis in a S_N1-reaction.

Funder

European Social Fund

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CC/C8CC06823B

Reference33 articles.

1. Direct Nucleophilic S N 1‐Type Reactions of Alcohols

2. Recent approaches for C–C bond formation via direct dehydrative coupling strategies

3. Catalytic functionalization of tertiary alcohols to fully substituted carbon centres

4. Total Synthesis of Diazonamide A

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