@article { ISI:000338023000039,
	title = {Direct allylation of in situ generated aldehyde acyl anions by synergistic NHC and palladium catalysis},
	journal = {Angewandte Chemie-International Edition},
	volume = {53},
	number = {27},
	year = {2014},
	month = {JUL},
	pages = {7038-7042},
	publisher = {WILEY-V C H VERLAG GMBH},
	type = {Article},
	address = {BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY},
	abstract = {<p>The direct regioselective allylation of in situ generated aldehyde acyl anions has been achieved by synergistic NHC and Pd catalysis. It provides an efficient access to valuable beta,gamma-unsaturated ketones under mild reaction conditions starting from easily accessible allylic carbonates and aldehydes without any preactivation. The synergistic catalysis method demonstrated herein adds a new dimension to the area of metal-mediated C allylation.</p>},
	keywords = {aldehyde umpolung, C allylation, N-heterocyclic carbenes, Palladium, synergistic catalysis},
	issn = {1433-7851},
	doi = {10.1002/anie.201400623},
	author = {Ahire, Milind M. and Mhaske, Santosh B.}
}
