ICAR Research Data Repository for Knowledge Management
Cu(I)-Catalyzed Cycloaddition of Constrained Azido-Alkynes: Access to 12- to 17-Membered Monomeric Triazolophanes Incorporating Furanoside Rings
EPrints@IICB
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 |
|
| 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/ |
|