Cu(I)-Catalyzed Cycloaddition of Constrained Azido-Alkynes: Access to 12- to 17-Membered Monomeric Triazolophanes Incorporating Furanoside Rings

Ray, Ankur and K, Manoj and Bhadbhade, Mohan M and Mukhopadhyay, Ranjan and Bhattacharjya, Anup (2006) Cu(I)-Catalyzed Cycloaddition of Constrained Azido-Alkynes: Access to 12- to 17-Membered Monomeric Triazolophanes Incorporating Furanoside Rings. Tetrahedron Letters, 47 (16). pp. 2775-2778.

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    Abstract

    Abstract—A strained monomeric 12-membered triazolophane was formed by the Cu(I)-catalyzed intramolecular cycloaddition of an azide to an alkyne having a constrained tether incorporating an aromatic ring and a furanoside ring. Similar cycloadditions of azidoalkynes having ester, furanoside and peptidic tethers led to the formation of monomeric triazolophanes of higher ring sizes.

    Item Type: Article
    URI: http://www.eprints.iicb.res.in/id/eprint/1124
    Subjects: Chemistry
    Divisions: Indian Institute of Chemical Biology
    Depositing User: Mr Santanu Sadhukhan
    Date Deposited: 29 Dec 2011 12:52
    Last Modified: 03 Feb 2012 14:27
    Official URL: http://dx.doi.org/10.1016/j.tetlet.2006.02.068
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