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Cited by 244

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Enantioselective Organocatalytic Fluorination‐Induced Wagner–Meerwein Rearrangement

Open access
Romanov‐Michailidis, Fedor, Guénée, Laure, Alexakis, Alexandre·2013·Angewandte Chemie International Edition

Abstract

Cracked under strain: Strained allylic cyclobutanols and cyclopropanols readily undergo a ring expansion described by the title rearrangement. This reaction is promoted by catalytic amounts of 1 and displays high tolerance with respect to the substrate scope. The corresponding β-fluoro spiroketone products are isolated in high yields and with excellent stereoselectivities. EDG=electron-donating group, EWG=electron-withdrawing group.

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Metadata

Authors
Romanov‐Michailidis, F., Guénée, L., & Alexakis, A.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2013-07-14
Volume
52
Issue
35
Pages
9266-9270
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2161843563
Cited by
244
References
1
FWCI
13.76
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Enantioselective Organocatalytic Fluorination‐Induced Wagner–Meerwein Rearrangement. https://app.cochat.ai/papers/10.1002/anie.201303527
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Romanov‐Michailidis, F., Guénée, L., & Alexakis, A. (2013). Enantioselective Organocatalytic Fluorination‐Induced Wagner–Meerwein Rearrangement. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201303527

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