Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Renate van Well"'
Autor:
Amber L. Thompson, Agnieszka Michalik, Robert J. Nash, Francis X. Wilson, Renate van Well, Peter Johnson, George W. J. Fleet, Chu-Yi Yu, Xiang-Guo Hu, Richard I. Cooper, David J. Watkin
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 11, Pp o2904-o2905 (2009)
X-ray crystallographic analysis of the title hydrobromide salt, C10H20N+·Br−, of (1R,2S,3R,5R,8aR)-3-hydroxymethyl-5-methyloctahydroindolizine-1,2-diol defines the absolute and relative stereochemistry at the five chiral centres in steviamine, a n
Externí odkaz:
https://doaj.org/article/5291fcab05ff425dbeb8474867a68d7c
Autor:
Robert J. Nash, Sarah F. Jenkinson, Francis Xavier Wilson, Laurence Edmund Jones, Renate van Well, Agnieszka Michalik, Graeme Horne, Xiang-Guo Hu, George W. J. Fleet, Chu-Yi Yu, Atsushi Kato, Jackie Hollinshead
The novel iminosugar (1R,2S,3R,5R,8aR)-3-(hydroxymethyl)-5- methyloctahydroindolizine-1,2-diol (steviamine) was isolated from leaf material of Stevia rebaudiana and leaves and bulbs of Veltheimia capensis. This is the first report of an indolizidine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d2d202269a591988716f2b085f87e74
https://doi.org/10.1016/j.phytol.2010.04.004
https://doi.org/10.1016/j.phytol.2010.04.004
Autor:
Carole Eliane Andree Maillol, Richard Storer, Severine Danielle Poignant, Peter David Johnson, Renate van Well, Stephen Paul Wren, Jonathon M. Tinsley, Adam G. Lambert, Gary Nugent, Francis Xavier Wilson, Fraser J. Wilkes, Colin Richard Dorgan, Richard Vickers, Graham Michael Wynne, Cristina Lecci, Richard Joseph Pye, Olivier De Moor, Paul Damien Price
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 21:4828-4831
Families of 2-arylbenzotriazoles and 2-arylindazoles that show positive effects in screens predictive of endogenous utrophin upregulation have been identified. Synthesis and structure-activity relationships are described leading to compounds with att
Publikováno v:
Tetrahedron Letters. 40:589-592
Mild conditions (1.2 eq. Hg(OAc)2, 1.2 eq. TBAF in 1:1 MeOH/THF; 35 min at 0 °C) have been developed for the protodesilylation of α-dimethylphenylsilyl esters. An enolate-dependent mechanism for the reaction was supported through studies indicating
Autor:
Graeme Horne, Fraser J. Wilkes, Richard Storer, Francis Xavier Wilson, Lindsay Fowler, Louise Czemerys, Renate van Well, Colin Richard Dorgan, Jon Tinsley
Publikováno v:
Alzheimer's & Dementia. 8
Autor:
Renate van Well, Graeme Horne, George W. J. Fleet, Francis Xavier Wilson, Wei Zhang, Robert J. Nash, Xiang-Guo Hu, Kasumi Sato, Chu-Yi Yu, Yue-Mei Jia, Atsushi Kato
Publikováno v:
Organic letters. 13(16)
Total synthesis of the proposed structure of (-)-hyacinthacine C(5) and its epimers at C6 and C7 is described. A key step of the synthesis was the construction of the bicyclic pyrrolizidine system by means of a nucleophilic addition of a dithiane to
Autor:
Graeme Horne, Francis Xavier Wilson, Sihong Chen, Jon Tinsley, Renate van Well, Fraser J. Wilkes
Publikováno v:
Alzheimer's & Dementia. 7
Autor:
Atsushi Kato, Xiang-Guo Hu, Shinpei Nakagawa, Yue-Mei Jia, Barbara Batholomew, George W. J. Fleet, Robert J. Nash, Francis Xavier Wilson, Chu-Yi Yu, Renate van Well
Publikováno v:
ChemInform. 41
Publikováno v:
ChemInform. 30
Mild conditions (1.2 eq. Hg(OAc)2, 1.2 eq. TBAF in 1:1 MeOH/THF; 35 min at 0 °C) have been developed for the protodesilylation of α-dimethylphenylsilyl esters. An enolate-dependent mechanism for the reaction was supported through studies indicating
Autor:
Richard I. Cooper, Chu-Yi Yu, Renate van Well, Xiang-Guo Hu, George W. J. Fleet, Francis Xavier Wilson, Robert J. Nash, David J. Watkin, Agnieszka Michalik, Amber L. Thompson, Peter David Johnson
Publikováno v:
Acta Crystallographica Section E: Structure Reports
Acta Crystallographica Section E, Vol 65, Iss 11, Pp o2904-o2905 (2009)
Acta Crystallographica Section E, Vol 65, Iss 11, Pp o2904-o2905 (2009)
X-ray crystallographic analysis of the title hydrobromide salt, C10H20N+·Br−, of (1R,2S,3R,5R,8aR)-3-hydroxymethyl-5-methyloctahydroindolizine-1,2-diol defines the absolute and relative stereochemistry at the five chiral centres in steviamine, a n