Regioselective formation of naphtho[2,1- <i>b</i> ]selenophenes <i>via</i> cascade cyclization of 1,3-diynylpropargyl alcohols promoted by iron( <scp>iii</scp> ) chloride and diorganyl diselenides

An iron( iii )-mediated method enables the efficient construction of naphthoselenophenes through a cascade cyclization of 1,3-diynylpropargyl alcohols and diorganyl diselenides.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo01195g
Primary Topic
Organic Chemistry Cycloaddition Reactions
Type
article
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article

Regioselective formation of naphtho[2,1- b ]selenophenes via cascade cyclization of 1,3-diynylpropargyl alcohols promoted by iron( iii ) chloride and diorganyl diselenides

Cristina W. Nogueira, Davi F. Back, Gilson Zeni, Pedro Pauletto
Organic Chemistry Frontiers
Organic Chemistry Cycloaddition Reactions
article

Regioselective formation of naphtho[2,1- b ]selenophenes via cascade cyclization of 1,3-diynylpropargyl alcohols promoted by iron( iii ) chloride and diorganyl diselenides

Cristina W. Nogueira, Davi F. Back, Gilson Zeni, Pedro Pauletto
article en

Abstract

An iron( iii )-mediated method enables the efficient construction of naphthoselenophenes through a cascade cyclization of 1,3-diynylpropargyl alcohols and diorganyl diselenides.

Organic Chemistry FrontiersVol. 12(24)
Universidade Federal de Santa Maria (BR), Franciscan University (BR)
Openalex Percentile: Top 82%
Organic Chemistry Cycloaddition Reactions
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