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 Activation of Carbonyl
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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