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Aroyl group driven [1,2] phosphonate-phosphate/phosphine oxide-phosphinate rearrangement
- Source :
- Tetrahedron. 72:4273-4279
- Publication Year :
- 2016
- Publisher :
- Elsevier BV, 2016.
-
Abstract
- Aroyl group driven phosphonate-phosphate rearrangement in dialkyl/aryl(α-hydroxy-β-oxo-β-arylethyl)phosphonates having α-proton under basic conditions is presented and extended to a novel one-pot direct coupling method between 2-oxoaldehydes (2OA) and H -phosphonates/diphenylphosphine oxide. The one-pot coupling reaction has an advantage in terms of using commercially available substrates and its broad substrate scope. The reactions between 2OAs and diphenylphosphine oxide represent a unique phosphine oxide-phosphinate rearrangement.
- Subjects :
- Phosphine oxide
010405 organic chemistry
Kornblum–DeLaMare rearrangement
Organic Chemistry
Sigmatropic reaction
Phosphinate
010402 general chemistry
Diphenylphosphine oxide
01 natural sciences
Biochemistry
Phosphonate
Medicinal chemistry
Carroll rearrangement
Coupling reaction
0104 chemical sciences
chemistry.chemical_compound
chemistry
Drug Discovery
Organic chemistry
Subjects
Details
- ISSN :
- 00404020
- Volume :
- 72
- Database :
- OpenAIRE
- Journal :
- Tetrahedron
- Accession number :
- edsair.doi...........11a1c1cbc3e1208a1574f52103561ef1
- Full Text :
- https://doi.org/10.1016/j.tet.2016.05.067