Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Matthew R. Hester"'
2
Solvent and in situ catalyst preparation impacts upon Noyori reductions of aryl-chloromethyl ketones: application to syntheses of chiral 2-amino-1-aryl-ethanols
Autor: Richard A. Hohler, Taylor Wendy Dianne, Paul M. Herrinton, Eric P. Seest, Steven P. Tanis, Bruce Roy Evans, Matthew R. Hester, Timothy Parker, James A. Nieman, Steven E. Heasley, Perrault William R, Lester A. Dolak
Publikováno v: Tetrahedron: Asymmetry. 17:2154-2182
As part of medicinal chemistry efforts we found it necessary to develop general syntheses of highly enantiomerically enriched 1-aryl-2-chloroethanols and 1-aryl-2-methylaminoethanols. A survey of literature methods suggested that a truly general appr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6482ae94ab6b6ee789870f20623ce22e
https://doi.org/10.1016/j.tetasy.2006.07.017
Zobrazit plný text záznamu
3
Discovery and initial development of a novel class of antibacterials: inhibitors of Staphylococcus aureus transcription/translation
Autor: Brian D. Wakefield, Gregg M. Kamilar, Michael T. Sweeney, Earline P. Melchior, Donna L. Romero, Scott D. Larsen, J. Craig Ruble, Keith R. Marotti, Matthew R. Hester
Publikováno v: Bioorganicmedicinal chemistry letters. 16(24)
The novel bacterial transcription/translation (TT) inhibitor 1 was identified through a combination of high throughput screening and exploratory medicinal chemistry. Initial optimization of the anthranilic acid moiety and sulfonamide amine diversity
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11645827c7e5bc1bd25528235a3717c7
https://pubmed.ncbi.nlm.nih.gov/17027262
Zobrazit plný text záznamu
4
ChemInform Abstract: 2,2′,7,7′-Tetrahydroxy-1,1′-Binaphthyl: A Versatile Chiral Spacer for Monotopic and Ditopic Cyclophane Hosts with Apolar Binding Sites
Autor: François Diederich, Mike A. Uyeki, Matthew R. Hester
Publikováno v: ChemInform. 21
Derivatives of 2,2′,7,7′-tetrahydroxy-1,1′-binaphthyl (5) are synthetically readily available chiral shapes with a major and a minor groove. Previous work by Cram et al. has shown that efficient chiral crown ether binding sites can be construct
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a8dfecdd4802425364e2a0d7d814a998
https://doi.org/10.1002/chin.199007221
Zobrazit plný text záznamu
6
2,2′,7,7′‐Tetrahydroxy‐1,1′‐Binaphthyl: A Versatile Chiral Spacer for Monotopic and Ditopic Cyclophane Hosts with Apolar Binding Sites
Autor: François Diederich, Mike A. Uyeki, Matthew R. Hester
Publikováno v: Israel Journal of Chemistry. 29:201-212
Derivatives of 2,2′,7,7′-tetrahydroxy-1,1′-binaphthyl (5) are synthetically readily available chiral shapes with a major and a minor groove. Previous work by Cram et al. has shown that efficient chiral crown ether binding sites can be construct
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::68634c1da9a39204c844d08eac3d81ac
https://doi.org/10.1002/ijch.198900028
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje