Novel route to functionalized indans via formal [3 + 2] cycloadditions of 1-benzylbenzotriazoles with alkenes

Article abstract of DOI:10.1080/00397919708004110

α-Functionalized 1-benzylbenzotriazoles (3, 4 and 12), derived from the lithiation of 1-(2,3-dimethoxybenzyl)benzotriazole 2 followed by reactions with electrophiles, or from the condensation of benzyl alcohol 11 with benzotriazole, undergo formal [3 + 2]

Full text of DOI:10.1080/00397919708004110

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Novel Route to Functionalized
Indans via Formal [3 +
2] Cycloadditions of 1-
Benzylbenzotriazoles with
Alkenes
Alan R. Katritzky a , Guifen Zhang a & Linghong Xie a
a Center for Heterocyclic Compounds, Department
of Chemistry , University of Florida , Gainesville, FL,
32611-7200, USA
Published online: 21 Aug 2006.
To cite this article: Alan R. Katritzky , Guifen Zhang & Linghong Xie (1997)
Novel Route to Functionalized Indans via Formal [3 + 2] Cycloadditions of 1-
Benzylbenzotriazoles with Alkenes, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 27:14, 2467-2478,
DOI: 10.1080/00397919708004110
To link to this article: http://dx.doi.org/10.1080/00397919708004110
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