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The First Asymmetric Intramolecular Stetter Reaction. Preliminary Communication

Enders, Dieter, Breuer, Klaus, Runsink, Jan, Teles, J. Henrique·1996·Helvetica Chimica Acta

Abstract

The first asymmetric intramolecular Stetter reaction is reported, using the chiral triazolium salt 1 as catalyst. Starting from the easily accessible 4‐(2‐formylphenoxy)but‐2‐enoates 2, this protocol opens up an enantioselective pathway to the benzo‐annulated pyran‐4‐ones (chroman‐4‐ones) 3a–h with good yields and enantiomeric excesses of up to 74%.

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Metadata

Authors
Enders, D., Breuer, K., Runsink, J., & Teles, J. H.
Venue
Helvetica Chimica Acta
Publisher
Wiley
Published
1996-10-30
Volume
79
Issue
7
Pages
1899-1902
ISSN
  • 0018-019X (ISSN-L)
  • 1522-2675
OpenAlex
W1545014673
Cited by
301
References
0
FWCI
3.89
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: The First Asymmetric Intramolecular Stetter Reaction. Preliminary Communication. https://app.cochat.ai/papers/10.1002/hlca.19960790712
The paper
Enders, D., Breuer, K., Runsink, J., & Teles, J. H. (1996). The First Asymmetric Intramolecular Stetter Reaction. Preliminary Communication. Helvetica Chimica Acta. https://doi.org/10.1002/hlca.19960790712

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

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.