Enantioselective organocatalytic activation of vinylidene–quinone methides (VQMs)-Reference-Cited by-同舟云学术

Enantioselective organocatalytic activation of vinylidene–quinone methides (VQMs)

Published:2019 Issue:75 Volume:55 Page:11168-11170
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Rodriguez Jean¹²³⁴⁵^ORCID,Bonne Damien¹²³⁴⁵^ORCID

Affiliation:

1. Aix Marseille Université

2. CNRS

3. Centrale Marseille

4. iSm2

5. Marseille

Abstract

Vinylidene–quinone methides (VQMs) are highly electrophilic chiral reagents that can be generated in situ from 2-(phenylethynyl)phenols. Their specific reactivity has revealed innovative strategies notably for the control of axial chirality.

Funder

Centre National de la Recherche Scientifique

Aix-Marseille Université

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/2019/CC/C9CC05097C

Reference17 articles.

1. Vinylidene–Quinone Methides, Photochemical Generation and β-Silicon Effect on Reactivity

2. A novel tandem bicyclization to form an indenopyran ring system

3. Unusual Oxaphosphoranes by Acyl Transfer fromo-Acetoxy-o′-diphenylphosphanyltolane

4. Vinylidene ortho-Quinone Methides: Unique Chiral Reaction Intermediates in Catalytic Asymmetric Synthesis

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