@article { ISI:000338988800008,
	title = {Copper(I) bromide-catalyzed carbonylative coupling of aryl halides with phenols, alcohols and amines using sodium cyanide as C-1 source: a synthesis of carboxylic acid derivatives},
	journal = {Advanced Synthesis \& Catalysis},
	volume = {356},
	number = {10},
	year = {2014},
	month = {JUL},
	pages = {2231-2238},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY},
	abstract = {<p>A new {\textquoteleft}{\textquoteleft}carbon monoxide-free{\textquoteright}{\textquoteright} synthesis of carboxylate derivatives via carbonylative coupling of aryl bromides with phenols, alcohols, amines and acids in the presence of copper(I) bromide as catalyst and sodium cyanide in a stoichiometric amount has been developed. Its intramolecular version provides for the preparation of lactones (e.g., isochroman-1-ones and isobenzfuranones), imides, anhydrides and lactams in excellent yields (73-96\%).</p>},
	keywords = {anhydrides, C-1 building blocks, isochroman-1-ones, lactams, lactones},
	issn = {1615-4150},
	doi = {10.1002/adsc.201301155},
	author = {Prasad, Pragati K. and Sudalai, Arumugam}
}
@article { ISI:000350219700005,
	title = {Synthesis of yangjinhualine A},
	journal = {Synthesis-Stuttgart},
	volume = {47},
	number = {4},
	year = {2015},
	month = {FEB},
	pages = {485-488},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>Selective reduction of 3-(4-hydroxyphenyl)-2-methylmaleic anhydride provides access the corresponding gamma-hydroxybutenolide natural product yangjinhualine A.</p>},
	keywords = {anhydrides, lactones, Natural products, reduction, Regioselectivity},
	issn = {0039-7881},
	doi = {10.1055/s-0034-1379582},
	author = {Deore, Prashant S. and Batwal, Ramesh U. and N. P. Argade}
}
