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Synlett 1991; 1991(10): 743-744
DOI: 10.1055/s-1991-34766
DOI: 10.1055/s-1991-34766
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.
Alkylation of Phospha-ylid Complexes. Application to the Synthesis of 1-Chlorophosphirane
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Publikationsdatum:
13. März 2002 (online)
[Phenyl(tributylphosphoranylidene)phosphine]pentacarbonyltungsten, W(CO)5(Bu3P=PPh), reacts with iodomethane and methanol to give [phenyl(methyl)(methoxy)phosphine]-pentacarbonyltungsten via initial alkylation of the complexed phosphorus atom and cleavage of the P-P bond. Self-alkylation spontaneously takes place in 4-chlorobutyl- and 2-chloroethyl(tributylphosphoranylidene)phosphine-tungsten complexes, leading to (1-chlorophospholane)pentacarbonyltungsten and to free 1-chlorophosphirane, respectively.