@article {2507,
	title = {Regioselective Reduction of 2,4-Diacylpyrroles and the Synthesis of a 2,4-Divinylpyrrole},
	journal = {European Journal of Organic Chemistry},
	number = {21},
	year = {2009},
	note = {ISI Document Delivery No.: 478ASTimes Cited: 0Cited Reference Count: 18Lin, Yan Dolphin, David},
	month = {Jul},
	pages = {3562-3566},
	type = {Article},
	abstract = {Reduction of 2,4-diacylpyrroles followed by dehydration to prepare the divinylpyrroles has been studied. The N-phenylsulfonyl group exhibited directing ability at the 4-position during the reduction of 2,4-diacylpyrrole and complete regioselectivity was achieved for formations of the 2- and 4-carbinols; several new derivatives, including 2,4-divinylpyrrole, have been prepared. ((C) Wiley-VCH Verlag GmbH \& Co. KGaA, 69451 Weinheim, Germany, 2009)},
	keywords = {DERIVATIVES, N Heterocycles, porphyrins, PYRROLES, QUARARIBEA METABOLITES, REDUCTION, regioselectivity, SUBSTITUENTS},
	isbn = {1434-193X},
	url = {<Go to ISI>://000268560700010},
	author = {Lin, Y. and Dolphin, D.}
}
