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Hydrostannylation of phosphaalkenes [1]

✍ Scribed by Marion Schmitz; Stefan Leininger; Uwe Bergsträßer; Manfred Regitz


Book ID
101259827
Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
241 KB
Volume
9
Category
Article
ISSN
1042-7163

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✦ Synopsis


Hydrostannylation reactions of the phosphaalkenes 9,11, and 21 with the triorganotin hydrides 1 proceed by different routes. Whereas the triorganotin hydrides 1a,b undergo regioselective 1,2addition to the P/C double bond of the P-aminophosphaalkene 9 to furnish the 2-stannylphosphanes 17a,b, the 1,2-addition products to the Phalophosphaalkenes 11 and 21 can only be postulated as the reactive intermediates 20 and 23, respectively. The reactions of 11 with 1a,b proceed with cleavage of the triorganotin halide via the diphosphene 15 to furnish the cyclophosphanes 18 and 19. On the other hand, the hydrostannylation reactions of the phosphaalkene 21 are not selective, and the 1,3-diphosphetane 22 is isolated as one of the reaction products.


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