@article { ISI:000290075500029,
	title = {Syntheses and biological evaluation of new triazole-spirochromone conjugates as inhibitors of mycobacterium tuberculosis},
	journal = {Tetrahedron Letters},
	volume = {52},
	number = {18},
	year = {2011},
	month = {MAY},
	pages = {2387-2389},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A series of novel 1,2,3-triazole fused spirochromone conjugates have been synthesized bearing both spirochromone moiety as well as a 1,2,3-triazole moiety. Some of the compounds have exhibited potential activity against Mycobacterium tuberculosis (virulent strain H37Rv). In particular 5e proved to be the most potent derivative exhibiting MIC = 0.78 mu g/mL. (C) 2011 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Antitubercular activity, Click chemistry, Mycobacterium tuberculosis, Spirochromones},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2011.02.099},
	author = {Muthukrishnan, Murugan and Mujahid, Mohammad and Yogeeswari, P. and Sriram, D.}
}
