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

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Title Cu(I)-Catalyzed Cycloaddition of Constrained Azido-Alkynes:
Access to 12- to 17-Membered Monomeric Triazolophanes Incorporating Furanoside Rings
 
Creator Ray, Ankur
K, Manoj
Bhadbhade, Mohan M
Mukhopadhyay, Ranjan
Bhattacharjya, Anup
 
Subject Chemistry
 
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.
 
Date 2006
 
Type Article
PeerReviewed
 
Format application/pdf
 
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.
 
Relation http://dx.doi.org/10.1016/j.tetlet.2006.02.068
http://www.eprints.iicb.res.in/1124/