@article { ISI:000236438200026,
	title = {Cu(I)-catalyzed cycloaddition of constrained azido-alkynes: access to 12- to 17-membered monomeric triazolophanes incorporating furanoside rings},
	journal = {Tetrahedron Letters},
	volume = {47},
	number = {16},
	year = {2006},
	month = {APR},
	pages = {2775-2778},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>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.</p>},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2006.02.068},
	author = {Ray, A. and Manoj, Kochunnoonny and Bhadbhade, Mohan M. and Mukhopadhyay, R. and Bhattacharjya, A.}
}
