Cu(I)-Catalyzed Cycloaddition of Constrained Azido-Alkynes: Access to 12- to 17-Membered Monomeric Triazolophanes Incorporating Furanoside Rings
IR@IICB: CSIR-Indian Institute of Chemical Biology, Kolkata
View Archive Info| Field | Value | |
| Title |
Cu(I)-Catalyzed Cycloaddition of Constrained Azido-Alkynes:
Access to 12- to 17-Membered Monomeric Triazolophanes Incorporating Furanoside Rings
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| Creator |
Ray, Ankur
K, Manoj Bhadbhade, Mohan M Mukhopadhyay, Ranjan Bhattacharjya, Anup |
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| Subject |
Chemistry
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| Description |
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.
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| Date |
2006
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| Type |
Article
PeerReviewed |
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| Format |
application/pdf
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| Identifier |
http://www.eprints.iicb.res.in/1124/1/TETRAHEDRON_LETTERS__Volume_47___Issue_16___Pages_2775%2D2778___[101].pdf
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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| Relation |
http://dx.doi.org/10.1016/j.tetlet.2006.02.068
http://www.eprints.iicb.res.in/1124/ |
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