Cu(I)-catalyzed cycloaddition of constrained azido-alkynes: access to 12- to 17-membered monomeric triazolophanes incorporating furanoside rings
Title | Cu(I)-catalyzed cycloaddition of constrained azido-alkynes: access to 12- to 17-membered monomeric triazolophanes incorporating furanoside rings |
Publication Type | Journal Article |
Year of Publication | 2006 |
Authors | Ray, A, Manoj, K, Bhadbhade, MM, Mukhopadhyay, R, Bhattacharjya, A |
Journal | Tetrahedron Letters |
Volume | 47 |
Issue | 16 |
Pagination | 2775-2778 |
Date Published | APR |
Type of Article | Article |
ISSN | 0040-4039 |
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 ail aromatic ring and a furanoside ring. Similar cycloadditions of azido-alkynes having ester, furanoside and peptidic tethers led to the formation of monomeric triazolophanes of higher ring sizes. (c) 2006 Elsevier Ltd. All rights reserved. |
DOI | 10.1016/j.tetlet.2006.02.068 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 2.347 |
Divison category:
Biochemical Sciences