Convenient one-step construction of fused or zwitterionic indanes from tetraynes

A straightforward technique has been developed for the construction of fused or zwitterionic indanes <i>via</i> a one-pot, cascade hexadehydro-Diels-Alder (HDDA) reaction of different functionalized tetraynes with nucleophilic reagents (vinyl carbazole or DMSO). The reaction proceeds under mild conditions with no metal catalysts, bases, or oxidants and exhibits excellent regioselectivity and high yields. A plausible reaction mechanism for the formation of zwitterionic indanes is proposed based on literatures and isolated fused indanes.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob00370a
Citations
1
Primary Topic
Cyclization and Aryne Chemistry
Type
article
Field-Weighted Citation Impact
0.94
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article

Convenient one-step construction of fused or zwitterionic indanes from tetraynes

Fenhua Wang, Chencheng Liu, Yao Tong, Qinghai Li
1 citations
Organic & Biomolecular Chemistry
Cyclization and Aryne Chemistry
0.94
article

Convenient one-step construction of fused or zwitterionic indanes from tetraynes

Fenhua Wang, Chencheng Liu, Yao Tong, Qinghai Li
article en
1 citations

Abstract

A straightforward technique has been developed for the construction of fused or zwitterionic indanes <i>via</i> a one-pot, cascade hexadehydro-Diels-Alder (HDDA) reaction of different functionalized tetraynes with nucleophilic reagents (vinyl carbazole or DMSO). The reaction proceeds under mild conditions with no metal catalysts, bases, or oxidants and exhibits excellent regioselectivity and high yields. A plausible reaction mechanism for the formation of zwitterionic indanes is proposed based on literatures and isolated fused indanes.

Organic & Biomolecular ChemistryVol. 23(20)
Anhui Polytechnic University (CN)
Openalex Percentile: Top 27%
Cyclization and Aryne Chemistry
0.94
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