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Isomerization in phosphaallyl systems. II. Prototropic rearrangement in the triad >C. /over bond P. /over bond C<

Journal Article · · J. Gen. Chem. USSR (Engl. Transl.); (United States)
OSTI ID:5571225
Stable compounds of 2-coordinate phosphorus were synthesized, namely, (bis(trimethylsilyl)methyl)fluorenylidenephosphine and (bis(trimethylsilyl)methylene)fluorenylphosphine, which are isomers differing in the position of the hydrogen atom in the triad .C .../over bond P .../over bond C. 1,3-Prototropic alkylphosphaalkene rearrangement was effected. 1,3-Prototropic migration in the triad C .../over bond P .../over bond C is limited by the high energy barrier present and is distinguished by low prototropic mobility. Strong bases (diazabicycloundecane, (bis(trimethylsilyl)amino)lithium) catalyze alkylphosphaalkene rearrangement.
Research Organization:
Institute of Organic Chemistry, Kiev, USSR
OSTI ID:
5571225
Journal Information:
J. Gen. Chem. USSR (Engl. Transl.); (United States), Journal Name: J. Gen. Chem. USSR (Engl. Transl.); (United States) Vol. 55:10; ISSN JGCHA
Country of Publication:
United States
Language:
English

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