Zobrazeno 1 - 5
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pro vyhledávání: '"Matthew Robert Johnson"'
Publikováno v:
Frontiers in Human Neuroscience, Vol 8 (2014)
We used a multi-voxel classification analysis of functional magnetic resonance imaging (fMRI) data to determine to what extent item-specific information about complex natural scenes is represented in several category-selective areas of human extrastr
Externí odkaz:
https://doaj.org/article/5a88cf82fa5142e78469008fe929bd7c
Autor:
Matthew Robert Johnson, Rajesh A. Shenoy, Van-Duc Le, Jolicia F. Gauuan, Howard Roark, James M. Hamby, Cheng Guo, Peter R. Guzzo, Michael Stier, John E. Mangette
Publikováno v:
Synthetic Communications. 41:2769-2793
As part of a medicinal chemistry collaboration, a number of novel bi- and tricyclic α-amino acids were prepared through various routes and characterized by 1H nuclear Overhauser effect difference experiments. The syntheses provide a number of routes
Autor:
Howard Roark, Matthew Robert Johnson, Michael Stier, Thomas Capiris, Peter R. Guzzo, Thomas Richard Belliotti, John E. Mangette, Van-Duc Le, Rajesh A. Shenoy
Publikováno v:
Tetrahedron. 65:9536-9541
Optically active α-amino 4H-[1,2,4]oxadiazol-5-ones (oxadiazolones) were prepared from optically active α-amino acids in five synthetic steps. The oxadiazolone moiety serves as a bioisosteric replacement for the carboxylic acid. Incorporation of an
Publikováno v:
Frontiers in Human Neuroscience
Frontiers in Human Neuroscience, Vol 8 (2014)
Frontiers in Human Neuroscience, Vol 8 (2014)
We used a multi-voxel classification analysis of functional magnetic resonance imaging (fMRI) data to determine to what extent item-specific information about complex natural scenes is represented in several category-selective areas of human extrastr
Autor:
Thomas Richard Belliotti, Rajesh A. Shenoy, Howard Roark, Van-Duc Le, Thomas Capiris, John E. Mangette, Peter R. Guzzo, Michael Stier, Matthew Robert Johnson
Publikováno v:
ChemInform. 41
Optically active α-amino 4H-[1,2,4]oxadiazol-5-ones (oxadiazolones) were prepared from optically active α-amino acids in five synthetic steps. The oxadiazolone moiety serves as a bioisosteric replacement for the carboxylic acid. Incorporation of an