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Cited by 192

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Asymmetric Epoxidation of Enones With Oxygen in the Presence of Diethylzinc and (R,R)‐N‐Methylpseudoephedrine

Enders, Dieter, Zhu, Jiqun, Raabe, Gerhard·1996·Angewandte Chemie International Edition in English

Abstract

An efficient method for the asymmetric epoxidation of α,β-unsaturated ketones 1 is embodied in their reaction with oxygen in the presence of diethylzinc and (R,R)-N-methyl-pseudoephedrine. It affords epoxides 2 in excellent yields, with complete diastereoselectivity, and with enantiomeric excesses of up to 92% ee. The enantiomerically pure amino alcohol employed can be recovered virtually quantitatively with unchanged optical purity.

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Crossref · 10.1002/anie.199617251

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Metadata

Authors
Enders, D., Zhu, J., & Raabe, G.
Venue
Angewandte Chemie International Edition in English
Publisher
Wiley
Published
1996-08
Volume
35
Issue
15
Pages
1725-1728
ISSN
0570-0833 (ISSN-L)
OpenAlex
W2078424995
Cited by
192
References
2
FWCI
7.78
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Asymmetric Epoxidation of Enones With Oxygen in the Presence of Diethylzinc and (R,R)‐N‐Methylpseudoephedrine. https://app.cochat.ai/papers/10.1002/anie.199617251
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Enders, D., Zhu, J., & Raabe, G. (1996). Asymmetric Epoxidation of Enones With Oxygen in the Presence of Diethylzinc and (R,R)‐N‐Methylpseudoephedrine. Angewandte Chemie International Edition in English. https://doi.org/10.1002/anie.199617251

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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