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A facile synthesis of stable 1,4-diionic phosphorus compounds
Stable crystalline phosphorus betaines are obtained from the 1:1:1 addition reaction between triphenylphosphine and ethyl propiolate in presence of strong CH-acids, such as N, N-dimethylbarbituric acid, Meldrum's acid or indan-1,3-dione. Stable crystalline phosphorus betaines are obtained from...
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Published in: | Tetrahedron letters 1998-06, Vol.39 (25), p.4579-4580 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Stable crystalline phosphorus betaines are obtained from the 1:1:1 addition reaction between triphenylphosphine and ethyl propiolate in presence of strong CH-acids, such as
N,
N-dimethylbarbituric acid, Meldrum's acid or indan-1,3-dione.
Stable crystalline phosphorus betaines are obtained from the 1:1:1 addition reaction between triphenylphosphine and ethyl propiolate in presence of
N,
N′-dimethylbarbituric acid. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/S0040-4039(98)00811-9 |