@article { ISI:000227273200009,
	title = {Novel one-pot synthesis of 2-Aryl-4(3H)-quinazolinones using room temperature ionic liquid as reaction medium as well as promoter},
	journal = {Synthetic Communications},
	volume = {35},
	number = {2},
	year = {2005},
	month = {JUL},
	pages = {231-241},
	publisher = {MARCEL DEKKER INC},
	type = {Article},
	address = {270 MADISON AVE, NEW YORK, NY 10016 USA},
	abstract = {<p>An efficient one-pot synthesis of 2-aryl-4(3H)-quinazolinones from 2-amino benzamides and substituted benzoyl chlorides in a room temperature ionic liquid is described. Compared with the classical reaction conditions, this new synthetic method has the advantages of recyclability of ionic liquid, very good to excellent yields (78-92\%), the absence of hazardous and expensive catalysts, and easy workup procedures giving rise to a process with minimum waste.</p>},
	keywords = {2-amino benzamide, 2-aryl-4(3H)-quinazolinones, benzoyl chlorides, Ionic liquid},
	issn = {0039-7911},
	doi = {10.1081/SCC-200048433},
	author = {Potewar, T. M. and Nadaf, R. N. and Daniel, Thomas and Lahoti, Rajgopal J. and Srinivasan, K. V.}
}
@article { ISI:000253625100010,
	title = {Novel stereoselective synthesis of pachastrissamine (jaspine B) starting from 1-pentadecanol},
	journal = {Tetrahedron-Asymmetry},
	volume = {19},
	number = {2},
	year = {2008},
	month = {FEB},
	pages = {209+},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A novel stereoselective synthesis of pachastrissamine (jaspine B), starting from commercially available 1-pentadecanol is described. Sharpless asymmetric dihydroxylation and a chelation controlled vinyl Grignard reaction are the key steps in this synthetic strategy. (C) 2007 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2007.12.001},
	author = {Venkatesan, K. and Srinivasan, K. V.}
}
