1987
DOI: 10.1016/s0040-4039(00)95919-7
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1,3λ3-Azaphosphinine durch umsetzung von 3-azapyryliumsalzen mit tris(trimethylsilyl)phosphan

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Cited by 63 publications
(8 citation statements)
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“…Among azaphosphinines, the 1,4-derivative was reported firstalthough only in solutionby Märkl and Matthes . The first derivative stable enough for isolation was 1,3-azaphosphinine . For the 1,2-aza- and 1,3,2-diazaphosphinines, an efficient synthesis has been designed recently .…”
Section: Azaphosphininesmentioning
confidence: 99%
“…Among azaphosphinines, the 1,4-derivative was reported firstalthough only in solutionby Märkl and Matthes . The first derivative stable enough for isolation was 1,3-azaphosphinine . For the 1,2-aza- and 1,3,2-diazaphosphinines, an efficient synthesis has been designed recently .…”
Section: Azaphosphininesmentioning
confidence: 99%
“…More interestingly, their reaction with alkynes affords 1,2-azaphosphinines 12 with extrusion of one molecule of nitrile. This [4 + 2] cycloaddition−cycloreversion process mimics the conversion of 1,3-azaphosphinines into phosphinines. ,, Upon further heating at higher temperature with a second equivalent of alkyne, these 1,2-azaphosphinines can, in turn, be converted into phosphinines. In such a way, we have prepared several polyfunctional phosphinines, as shown in the following equation (eq 3).
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mentioning
confidence: 98%
“…Whereas all of the possible azaphosphinines are known to date, our knowledge of diazaphosphinines is presently limited to a couple of examples . We wish to describe here a very simple access to 1,3,2-diazaphosphinines and their use to prepare 1,2-azaphosphinines and polyfunctional phosphinines.…”
mentioning
confidence: 99%
“…Whereas all of the possible azaphosphinines are known to date [18,19], our knowledge of diazaphosphinines is presently limited [20]. We wish to describe here a very simple route to 1,3,2-diazaphosphinine derivative.…”
Section: Resultsmentioning
confidence: 99%