Journal of the American Chemical Society p. 2497 - 2501 (1982)
Update date:2022-08-03
Topics: Oxidation Cyclization Product Formation Nucleophilic Attack Carbonyl Compounds Trivalent Phosphorus Compounds Oxidants
Harper, S. D.
Arguengo, Anthony J.
Phosphonous diesters derived from the reaction of phenylphosphonous dichloride with 2-ketophenols readily undergo head-to-tail intramolecular cyclization in cases where the carbonyl function is an aldehyde, trifluoromethylacetophenone, or diaryl ketone.A
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Doi:10.1055/s-1982-29760
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