@article { ISI:000304387800025,
	title = {Efficient total synthesis of calothrixin B},
	journal = {Tetrahedron Letters},
	volume = {53},
	number = {23},
	year = {2012},
	month = {JUN},
	pages = {2894-2896},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient synthesis of calothrixin B (2) is demonstrated starting from 9H-carbazol-4-ol, having two one-pot reaction sequences as key steps. As a novel observation, DMF-methanol was shown to be a hydride donor for reduction of aldehyde to alcohol. Unexpectedly, nucleophilic substitution of benzyloxy by methoxy group was observed. (C) 2012 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Calothrixin B, CAN, DMF-methanol, Hydride donor},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2012.03.131},
	author = {Bhosale, Shrikar M. and Gawade, Rupesh L. and Puranik, Vedavati G. and Kusurkar, Radhika S.}
}
