Zobrazeno 1 - 10
of 64
pro vyhledávání: '"J. T. Pinhey"'
Autor:
J. T. Pinhey
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0287b1e3ab7ef403b784fe1aedc8a3b1
https://doi.org/10.1002/chin.199203306
https://doi.org/10.1002/chin.199203306
Autor:
J. T. Pinhey, C. J. Parkinson
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::576291d9699dae280ec4c43fc29b0a5f
https://doi.org/10.1002/chin.199133274
https://doi.org/10.1002/chin.199133274
Autor:
M.-L. Huber, J. T. Pinhey
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a98c5098e5b4d45b6d547d1d08a0aed
https://doi.org/10.1002/chin.199027141
https://doi.org/10.1002/chin.199027141
Autor:
J. T. Pinhey, J. Morgan
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d5f016ff22bc572c45faadc11a8d87b
https://doi.org/10.1002/chin.199027140
https://doi.org/10.1002/chin.199027140
Autor:
J. T. Pinhey, R. O. Hellyer
Publikováno v:
J. Chem. Soc. C. :1496-1498
The structure 5-hydroxy-2,2,6,6-tetramethyl-4-(β-phenylpropionyl)cyclohex-4-ene-1,3-dione (I) is suggested for grandiflorone, a new β-triketone, which occurs together with small amounts of leptospermone and flavesone in the essential oils of Leptos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3addfaded886c55bdcabaec3e07af81f
https://doi.org/10.1039/j39660001496
https://doi.org/10.1039/j39660001496
Autor:
J. T. Pinhey, E. Rizzardo
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :1358-1360
The compound described as ‘cholestane-3,4,6-trione’ by Windaus and Kuhr has been shown to be the 3-ethyl ether of the corresponding dienol. Although relatively stable to acid, the enol ether may be hydrolysed to yield the triketone, a mixture of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16279fc27aea146c40056128be698189
https://doi.org/10.1039/p19720001358
https://doi.org/10.1039/p19720001358
Publikováno v:
ChemInform. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74dc5ea0e935eb38b0d77456b1d6f18b
https://doi.org/10.1002/chin.198829185
https://doi.org/10.1002/chin.198829185
Autor:
J. C. Chapman, J. T. Pinhey
Publikováno v:
Chemischer Informationsdienst. 6
17-Oxo-18-nor-5α,13β-androstan-3β-yl acetate (6) and the 13α-epimer (7) have been synthesized by two routes, both of which involve initially an ?abnormal? Beckmann rearrangement of the oxime of 17-oxo-5α-androstan- 3β-yl acetate to the 13,17-se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cba116af934fd569e7d8352cd2a7e56f
https://doi.org/10.1002/chin.197507455
https://doi.org/10.1002/chin.197507455
Publikováno v:
Chemischer Informationsdienst. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7db93f9d242ae7a234af9c750fffdab7
https://doi.org/10.1002/chin.197707162
https://doi.org/10.1002/chin.197707162
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