Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Stanley D. Higgins"'
Autor:
Roger A. Whittaker, Stanley M. Roberts, Patrick D. Bailey, Stanley D. Higgins, Colin H. Ridyard, Georgina M. Rosair, Andrew J. Willets
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1811
Tricyclo [3.3.1,l3,7]decane 1a has been converted into 1-hydroxytricyclo [3.3.1.13.7] decane 1b, tricyclo[3.3.1.13.7]decane-1,4ax-diol 4b, tricyclo[3.3.1.13.7]decane-1,3-diol 3b and to a lesser extent, 2-hydroxytricyclo [3.3.1.13,7] decane 4a (20 to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8b3a9f1f13e99ce41a6338d9463bf10
https://doi.org/10.1039/p29960001811
https://doi.org/10.1039/p29960001811
Autor:
Colin H. Ridyard, Roger A. Whittaker, Andrew Willetts, Patrick D. Bailey, Stanley M. Roberts, Georgina M. Rosair, Stanley D. Higgins
Publikováno v:
Chemical Communications. :1833
The biohydroxylation of 1-substituted adamantanes using Absidia cylindrospora in a whole-cell oxidation system exclusively generated 3-hydroxy and 4ax-hydroxy derivatives; the assignments were confirmed by three X-ray crystal structure determinations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::798efbdaa147ea3fdf8ebf23c42e34d8
https://doi.org/10.1039/cc9960001833
https://doi.org/10.1039/cc9960001833
Autor:
Stanley D. Higgins, C. Barry Thomas
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :1483-1488
Further methods for effecting the oxidative rearrangement of 1-arylalkanones to α-arylalkanoic esters have been investigated. It has been shown that appropriate α-iodoacetals, readily prepared from the ketones, can be converted into esters on treat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a323b4941b9f3edf40f77ea1b349d35e
https://doi.org/10.1039/p19830001483
https://doi.org/10.1039/p19830001483
Conversion of aromatic ketones into π-arylalkanoic acids. Oxidation by thallium(III ) and by halogens
Autor:
C. Barry Thomas, Stanley D. Higgins
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :235-242
The mechanism by which thallium(III) nitrate oxidises aromatic ketones to α-arylalkanoic acids has been investigated and the role of additives in the system elucidated. It is found that in the absence of additives an organothallium intermediate, mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::383a9ade3c7c41769d28c6fbb1cb5f41
https://doi.org/10.1039/p19820000235
https://doi.org/10.1039/p19820000235
Autor:
H. T. Andrew Cheung, Lindsay Brown, John Boutagy, Richard Thomas, Stanley D. Higgins, C. Barry Thomas, Christian H. Gagnieu, Annie V. Grouiller, Majekodunmi O. Fatope, Joseph I. Okogun, Toshihiko Matsumoto, Shohei Inoue, Silvana Fatutta, Giuliana Pitacco, Claudio Russo, Ennio Valentin, Pier Giovanni Baraldi, Fabio Moroder, Gian Piero Pollini, Daniele Simoni, Achille Barco, Simonetta Benetti, Gerald Brooks, Eric Hunt
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :889
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a382cf8e6cf58a226ca5e10ad87b7008
https://doi.org/10.1039/p19830000889
https://doi.org/10.1039/p19830000889