Catalytic haloallylation/Zr-mediated dienyne cyclization/isomerization sequence for tailored cyclopentadiene substitution

A synthetic sequence leading to the controlled decoration of cyclopentadienes is reported. This approach allows site-selective installation of different functionalities around the Cp ring, exploiting stereoelectronic features of internal alkynes.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2024-11-27
DOI
https://doi.org/10.1039/d4qo02020k
Citations
2
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.32

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article

Catalytic haloallylation/Zr-mediated dienyne cyclization/isomerization sequence for tailored cyclopentadiene substitution

Ivana Nikšić‐Franjić, Nikola Topolovčan, Marko Gobin
2 citations
Organic Chemistry Frontiers
Asymmetric Hydrogenation and Catalysis
0.32
article

Catalytic haloallylation/Zr-mediated dienyne cyclization/isomerization sequence for tailored cyclopentadiene substitution

Ivana Nikšić‐Franjić, Nikola Topolovčan, Marko Gobin
article en
2 citations

Abstract

A synthetic sequence leading to the controlled decoration of cyclopentadienes is reported. This approach allows site-selective installation of different functionalities around the Cp ring, exploiting stereoelectronic features of internal alkynes.

Organic Chemistry FrontiersVol. 12(3)
Ruđer Bošković Institute (HR)
European Commission
Openalex Percentile: Top 48%
Asymmetric Hydrogenation and Catalysis
0.32
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