Zobrazeno 1 - 10
of 63
pro vyhledávání: '"P. W. Le Quesne"'
Publikováno v:
Pure and Applied Chemistry. 66:2249-2254
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::289a233bf69b0362e5dceeb1fde82181
https://doi.org/10.1351/pac199466102249
https://doi.org/10.1351/pac199466102249
Autor:
Miguel O. Mitchell, P. W. Le Quesne
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::513024d15043b651b194c775dbff2259
https://doi.org/10.1002/chin.199112331
https://doi.org/10.1002/chin.199112331
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5b711d5e97ad46ead6033b74a57f10c
https://doi.org/10.1002/chin.199508294
https://doi.org/10.1002/chin.199508294
Autor:
P. W. Le Quesne, Shao-Xia Yu
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7eb54b07e1aa843b21e75bf45af6b966
https://doi.org/10.1002/chin.199550202
https://doi.org/10.1002/chin.199550202
Publikováno v:
Analytical Chemistry. 64:1077-1087
Deuterium-labeled cholesterol is used to monitor for artifactually produced cholesterol oxidation products during analysis. [2H9]Cholesterol, labeled on the side chain, is added to the sample immediately upon isolation, and the ratios of labeled to u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47e3521224a0c274aab4f2109d07cd0c
https://doi.org/10.1021/ac00034a003
https://doi.org/10.1021/ac00034a003
Publikováno v:
Journal of Natural Products; July 2008, Vol. 71 Issue: 8 p1431-1440, 10p
Publikováno v:
Journal of Natural Products. 43:353-359
The major cytotoxic activity of crude extracts of Nectandra rigida Nees is due to dehydrodiisoeugenol,the sample isolated being slightly enriched in the dextrorotatory enantiomer. Galgravin and two new tetrahydrofuranoid lignans, nectandrin A and nec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7430ed80f0c3535fe1964543d52bf8b7
https://doi.org/10.1021/np50009a006
https://doi.org/10.1021/np50009a006
Publikováno v:
Biochemistry. 25:2065-2072
A mechanism is proposed for mixed-function oxidase-catalyzed formation of the catechol estrogens 2-hydroxy- and 4-hydroxyestradiol from estradiol. This mechanism involves nonaromatic epoxyenones as intermediates. The isomeric 1 alpha,2 alpha-epoxy-17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4b61a162544e18a417ca0e41fbff4d9
https://doi.org/10.1021/bi00356a035
https://doi.org/10.1021/bi00356a035
Publikováno v:
The Journal of Organic Chemistry. 36:83-87
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02e95aaf550792c852752418261e2e36
https://doi.org/10.1021/jo00800a019
https://doi.org/10.1021/jo00800a019
Publikováno v:
The Journal of Organic Chemistry. 38:237-240
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8e6d6c783036ba14407d8107b476307
https://doi.org/10.1021/jo00942a009
https://doi.org/10.1021/jo00942a009