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Formation of the cage-like phosphoranes with the P-C and P-N bonds in the reactions of 2-(2-benzylidenamino)phenoxy-4-tert-butylbenzo-1,3,2-dioxaphosphol with ethyl mesoxalate and ethyl trifluoropyruvate
Authors:M. N. Dimukhametov  V. F. Mironov  D. B. Krivolapov  E. V. Mironova  R. Z. Musin
Affiliation:1. A. E. Arbuzov Institute of Organic and Physical Chemistry Kazan Scientific Center of the Russian Academy of Sciences, 8 ul. Akad. Arbuzova, 420088, Kazan, Russian Federation
Abstract:The reaction of 2-(2-benzylidenamino)phenoxy-4-tert-butylbenzo-1,3,2-dioxaphosphol with ethyl mesoxalate and ethyl trifluoropyruvate resulted in the formation of tricyclic phosphoranes with the P-C and P-N bonds. The adduct emerged from the initial reaction of the PIII derivative with the activated ketone (1: 1), further underwent the transformation via the intramolecular reaction involving the benzylideniminoaryl substituent, which resulted in the formation of the cage-like phosphoranes.
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