@article {43481,
	title = {Fluoride-mediated dephosphonylation of alpha-diazo-beta-carbonyl phosphonates},
	journal = {Organic Letters},
	volume = {19},
	year = {2017},
	month = {JAN},
	pages = {372-375},
	abstract = {The possibility of fluoride-mediated selective dephosphonylation of alpha-diazo-beta-carbonyl phosphonates such as the Ohira-Bestmann reagent has been proposed and executed. The resulting alpha-diazocarbonyl intermediates undergo a (3 + 2)pcycloaddition at room temperature with conjugated olefins and benzynes. Interestingly, under the current conditions, the resulting cycloaddition products underwent either N-acylation (with excess alpha-diazo-beta-carbonyl phosphonates) or Michael addition (with conjugated olefins).},
	doi = {10.1021/acs.orglett.6b03573},
	author = {Phatake, Ravindra S. and Mullapudi, Venkannababu and Wakchaure, Vivek C. and Ramana, Chepuri V.}
}
