@article { ISI:000340152000016,
	title = {Facile synthesis of the isoquinoline alkaloids doryanine and oxyhydrastinine},
	journal = {Synthesis-Stuttgart},
	volume = {46},
	number = {14},
	year = {2014},
	month = {JUL},
	pages = {1954-1956},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>Starting from 4,5-(methylenedioxy)homophthalic acid, a concise and efficient synthesis of the isoquinoline alkaloids dory-anine and oxyhydrastinine is described via the corresponding homophthalimide utilizing a one-pot regioselective reductive dehydration and catalytic hydrogenation pathway.</p>},
	keywords = {dehydration, homophthalic acid, homophthalimide, isoquinoline alkaloids, regioselective reduction},
	issn = {0039-7881},
	doi = {10.1055/s-0033-1341158},
	author = {Jangir, Ravi and Gadre, Smita R. and N. P. Argade}
}
