Zobrazeno 1 - 4
of 4
pro vyhledávání: '"R. P. Kopinski"'
Publikováno v:
Chemischer Informationsdienst. 15
Derivatives of 2,2-dimethyl-1,3-dioxan-4,6-dione (Meldrum's acid) and the sodium salts of substituted malonic esters undergo electrophilic C-arylation in high yield with aryllead triacetates, thus providingnew routes to α-arylalkanoic acids. Synthes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbd2e17d2f5e8e5510b908fd903387ee
https://doi.org/10.1002/chin.198444101
https://doi.org/10.1002/chin.198444101
Autor:
R. P. Kopinski, J. T. Pinhey
Publikováno v:
Chemischer Informationsdienst. 14
The treatment of 4-benzoyltetrahydrofuran-2,3-dione (2a) with 2 equiv. of phenyllead triacetate (3a) in chloroform gives 1,2-diphenylpropenone (4a) in excellent yield. This reaction has been investigated with a number of similar derivatives of tetrah
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e07bf3857cbad4e29d7ccf54d3ef59ee
https://doi.org/10.1002/chin.198329140
https://doi.org/10.1002/chin.198329140
Autor:
R. P. Kopinski, J. T. Pinhey
Publikováno v:
Australian Journal of Chemistry. 36:311
The treatment of 4-benzoyltetrahydrofuran-2,3-dione (2a) with 2 equiv. of phenyllead triacetate (3a) in chloroform gives 1,2-diphenylpropenone (4a) in excellent yield. This reaction has been investigated with a number of similar derivatives of tetrah
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0105b138f0dd6a42e0d66f1964d0423
https://doi.org/10.1071/ch9830311
https://doi.org/10.1071/ch9830311
Publikováno v:
Australian Journal of Chemistry. 37:1245
Derivatives of 2,2-dimethyl-1,3-dioxan-4,6-dione (Meldrum's acid) and the sodium salts of substituted malonic esters undergo electrophilic C-arylation in high yield with aryllead triacetates, thus providingnew routes to α-arylalkanoic acids. Synthes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e4594d62b5bbea9c252ebc7300642ca
https://doi.org/10.1071/ch9841245
https://doi.org/10.1071/ch9841245