Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Steven J, Canipa"'
Autor:
Rachael E. Tennant, Richard V. Williams, Masamitsu Honma, Alex Cayley, Kenichi Masumura, Susanne A. Stalford, Sebastien J. Guesne, Steven J. Canipa, William C. Drewe, Takeshi Morita
Publikováno v:
Mutagenesis. 34:111-121
As part of the hazard and risk assessment of chemicals in man, it is important to assess the ability of a chemical to induce mutations in vivo. Because of the commonalities in the molecular initiating event, mutagenicity in vitro can correlate well t
Autor:
Rachael E. Tennant, Devin O'Brien, Thomas Steger-Hartmann, Jonathan D. Vessey, Steven J. Canipa, Ann De Smedt, Rachel Hemingway, Angela White, Martyn L. Chilton, Rahul Parakhia, Sylvain Etter, Jeffrey Plante, Jedd Hillegass, Janet Gould, Alun Myden, Paul Sterchele, Donna S. Macmillan, B. Smith
Publikováno v:
Journal of Applied Toxicology. 37:985-995
Dermal contact with chemicals may lead to an inflammatory reaction known as allergic contact dermatitis. Consequently, it is important to assess new and existing chemicals for their skin sensitizing potential and to mitigate exposure accordingly. The
Autor:
Lilia Fisk, Valerie J. Gillet, William C. Drewe, Mukesh Patel, Jonathan D. Vessey, Steven J. Canipa, Laurence Coquin, Richard Sherhod, Jeffrey Plante
Publikováno v:
Toxicology Research. 4:46-56
Emerging pattern mining techniques have been applied to datasets of Ames mutagens. The discovered patterns give rise to clusters of compounds from large and biased datasets which are used to develop new structural alerts for mutagenicity in the Derek
Publikováno v:
Angewandte Chemie (International ed. in English). 57(1)
An 8-step, gram-scale synthesis of the (-)-sparteine surrogate (22 % yield, with just 3 chromatographic purifications) and a 10-step, gram-scale synthesis of (-)-sparteine (31 % yield) are reported. Both syntheses proceed with complete diastereocontr
Publikováno v:
Tetrahedron. 70:7395-7403
Four new copper(II)/diamine complexes comprising some (+)-sparteine surrogates and a cyclohexane-derived diamine were prepared and evaluated as chiral catalysts in desymmetrisation of meso-diols and asymmetric Henry reactions. Mono-benzoylation react
Autor:
Steven J, Canipa, Martyn L, Chilton, Rachel, Hemingway, Donna S, Macmillan, Alun, Myden, Jeffrey P, Plante, Rachael E, Tennant, Jonathan D, Vessey, Thomas, Steger-Hartmann, Janet, Gould, Jedd, Hillegass, Sylvain, Etter, Benjamin P C, Smith, Angela, White, Paul, Sterchele, Ann, De Smedt, Devin, O'Brien, Rahul, Parakhia
Publikováno v:
Journal of applied toxicology : JAT. 37(8)
Dermal contact with chemicals may lead to an inflammatory reaction known as allergic contact dermatitis. Consequently, it is important to assess new and existing chemicals for their skin sensitizing potential and to mitigate exposure accordingly. The
Autor:
Steven J. Canipa, Donna S. Macmillan, Martyn L. Chilton, Barber Christopher Gordon, Richard V. Williams
Publikováno v:
Regulatory toxicology and pharmacology : RTP. 76
There is a pressing need for non-animal methods to predict skin sensitisation potential and a number of in chemico and in vitro assays have been designed with this in mind. However, some compounds can fall outside the applicability domain of these in
Publikováno v:
The Journal of Organic Chemistry. 76:4794-4799
A new protocol for the catalytic asymmetric deprotonation of a phosphine borane using s-BuLi and substoichiometric quantities of chiral diamines is reported. The method involves three sequential additions of s-BuLi, and use of (-)-sparteine or the (+
Publikováno v:
Toxicology Letters. 295:S174
Publikováno v:
Tetrahedron: Asymmetry. 20:2407-2412
The catalytic asymmetric deprotonation of tert-butyldimethylphosphine borane using s-BuLi or n-BuLi and sub-stoichiometric amounts of (−)-sparteine under one-ligand and two-ligand manifolds has been investigated. Using s-BuLi, slightly higher enant