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Synthesis 1997; 1997(4): 455-460
DOI: 10.1055/s-1997-1199
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Organophosphorus Compounds; 177.1 Hydrostannylation of Becker-Type Phosphaalkenes

Marion Schmitz, Rudolf Göller, Manfred Regitz*
  • *Fachbereich Chemie der Universität Kaiserslautern, Erwin-Schrödinger-Straße, D-67663 Kaiserslautern, Germany, Fax +49(631)2053921
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Publication Date:
31 December 2000 (online)

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Reactions of Becker-type phosphaalkenes 5a-e with triorganotin hydrides 1a,b proceed through 1,2-addition to furnish the stannylphosphanes 7a-j. Analogous use of the diorganotin dihydrides 11 and 14 gives rise to the hydridostannylphosphanes 12 and 15. The product 16 of a double addition can also be isolated from the reaction of dimethyltin dihydride 14 with the phosphaalkene 5a.

hydrostannylation - phosphaalkenes - 1,2-addition - triorganotin hydride - diorganotin dihydride

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