
Journal of Organometallic Chemistry p. 9 - 18 (1984)
Update date:2022-09-26
Topics:
Aboujaoude, Elie Elia
Collignon, Noel
Savignac, Philippe
Condensation of a lithiated phosphonate carbanion not bearing a stabilizing group with a carbonyl precursor (amide or ester) gives an intermediate oxyanion which decomposes on hydrolysis to yield a β-carbonyl phosphonate.This type of reaction gives access to a large group of phosphonates: β-ketophosphonates, phosphonic aldehydes, phosphonopyruvates etc.The reaction conditions are discussed.
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