1,2- and 1,3-diphosphetanes from alkylidenephosphines |
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Authors: | Gerd Becker Winfried Becker Gudrun Uhl Werner Uhl Hans-Jürgen Wessely |
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Affiliation: | Institut für Anorganische Chemie der Universit?t Stuttgart , Pfaffenwaldring 55, D-7000, Stuttgart 80 |
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Abstract: | ![]() Abstract Alkyl- or arylbis(trimethylsilyl)phosphines as well as tris(trimethylsilyl)phosphine and the corresponding arsines react with acyl chlorides to give [1-(trimethylsiloxy)alkylidene]phosphines 1 and -arsines 2; most of their 2,2-dimethylpropylidene derivatives are thermally stable at room temperature. With the same class of phosphines as starting compounds and carbon disulfide [bis(trimethylsilylsulfano)methylidene]phosphines 3 are formed, whereas [(dialkylamino)methylidene]-4 and [diarylmethylidene]phosphines 5 or the corresponding arsines 6 and 7 can be obtained from acyl amides or ketones.1 |
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Keywords: | Acid-base properties aminophosphonates extraction Kabachnik-Fieids reaction synthesis |
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