
Phosphorus, Sulfur and Silicon and the Related Elements p. 569 - 572 (1999)
Update date:2022-08-04
Topics:
Mastryukova, Tatyana A.
Aladzheva, Inga M.
Lobanov, Dmitrii I.
Bykhovskaya, Olga V.
Petrovskii, Pavel V.
Lyssenko, Konstantin A.
Kabachnik, Martin I.
The general pathway to 1,2-monoheterophosphacyclanes via intramolecular S-and N-alkylation of ω-halogenoalkylsubstituted thiophosphoryl and iminophosphoryl compounds has been developed. Intramolecular alkylation of 3-and 4-halogenoalkyldiphenylphosphine sulfides results in 1,2λ4-thiaphospholanium and thiaphosphorinanium halogenides. In solution of these compounds the rare ring-chain halogenotropic tautomerism has been observed and investigated in detail. Intramolecular Pishchimuka rearrangement of the esters of ω-halogenoalkylsubstituted thiophosphorus acids was found to be a synthetic route to 2-oxo-1,2ω5-thiaphospholanes and thiaphosphorinanes.
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