Zobrazeno 1 - 10
of 233
pro vyhledávání: '"William H. Pirkle"'
Autor:
Robert P. Sheridan, Patrick Piras, Edward C. Sherer, Christian Roussel, William H. Pirkle, Christopher J. Welch
Publikováno v:
Molecules, Vol 21, Iss 10, p 1297 (2016)
We apply matched molecular pair (MMP) analysis to data from ChirBase, which contains literature reports of chromatographic enantioseparations. For the 19 chiral stationary phases we examined, we were able to identify 289 sets of pairs where there is
Externí odkaz:
https://doaj.org/article/98a0f6ec51684acc887bfa73f669d151
Autor:
Christopher J. Welch, Patrick Piras, Christian Roussel, William H. Pirkle, Robert P. Sheridan, Edward C. Sherer
Publikováno v:
Molecules
Molecules, MDPI, 2016, 21 (10), ⟨10.3390/molecules21101297⟩
Molecules, 2016, 21 (10), ⟨10.3390/molecules21101297⟩
Molecules; Volume 21; Issue 10; Pages: 1297
Molecules, Vol 21, Iss 10, p 1297 (2016)
Molecules, MDPI, 2016, 21 (10), ⟨10.3390/molecules21101297⟩
Molecules, 2016, 21 (10), ⟨10.3390/molecules21101297⟩
Molecules; Volume 21; Issue 10; Pages: 1297
Molecules, Vol 21, Iss 10, p 1297 (2016)
International audience; We apply matched molecular pair (MMP) analysis to data from ChirBase, which contains literature reports of chromatographic enantioseparations. For the 19 chiral stationary phases we examined, we were able to identify 289 sets
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1211fd8c51f6ba14703d86eab2864f5
https://hal.archives-ouvertes.fr/hal-01442568
https://hal.archives-ouvertes.fr/hal-01442568
Publikováno v:
Bulletin of the Korean Chemical Society. 32:4423-4426
School of Chemical Sciences, University of Illinois, Urbana, IL 61801, USAReceived September 1, 2011, Accepted October 9, 2011Key Words : Enantiomer separation, Chiral self-recognition, Chiral stationary phasePioneering work in the design of brush-ty
Autor:
Huei-Shian Lin, James R. Carey, William H. Pirkle, Wonjae Lee, Phillip I. Volkers, Bin-Syuan Huang, William A. Boulanger, David A. Engebretson, Seth E. Snyder
Publikováno v:
Tetrahedron. 67:7143-7147
Chiral stationary phases were synthesized and their ability to separate racemic precursors from which they were derived was assessed. Taken in conjunction with homochiral recognition previously observed in the solid state, the results of this study r
Autor:
Wonjae Lee, William H. Pirkle
Publikováno v:
Bulletin of the Korean Chemical Society. 31:620-623
A brush type chiral stationary phase (CSP 2) derived from α-amino β-lactam was prepared for the separation of the enan- tiomers of β-blockers. Compared to the CSP derived from α-amino phosphonate (CSP 1), in general, the conforma- tionally rigid
Autor:
Elias Ndzie, Wilhelm Hauck, Olivier Ludemann-Hombouger, William H. Pirkle, Jean Blehaut, Scott R. Perrin, Roger-Marc Nicoud
Publikováno v:
Organic Process Research & Development. 11:817-824
An industrial process for the purification of metric tons of enantiomerically pure difluoromethylornithine (DFMO HCl) is described. The amino acid DFMO HCl is cyclized to form the lactam, which is acylated with pivaloyl chloride to form rac-N-pivaloy
Autor:
William H. Pirkle, Michael E. Koscho
Publikováno v:
Tetrahedron: Asymmetry. 16:3345-3351
A chiral solvating agent (CSA) based on the chiral selector used in the Whelk-O 1 chiral stationary phase (CSP) was prepared and its scope evaluated. This chiral selector possesses a cleft flanked with aromatic groups and produces upfield chemical sh
Publikováno v:
Tetrahedron: Asymmetry. 16:3147-3153
Designed to distinguish between the enantiomers of compounds possessing commonly occurring structural features, the chiral selector used in the chiral stationary phase (CSP) 1 (Whelk-O1) is broadly applicable. In an effort to further the understandin
Publikováno v:
Tetrahedron. 61:7562-7567
Enantioselective partitioning of racemic N-3,5-(dinitrobenzoyl)leucine or racemic naproxen was studied using a two-component chiral phase transfer approach. A combination of an achiral ion-pairing reagent and a chiral complexing agent (selector) is n
Publikováno v:
The Journal of Organic Chemistry. 70:4073-4081
[reaction: see text] A detailed study concerning the formation of Meisenheimer adducts in biphasic solvent systems is described. The process relies on utilizing a significantly lipophilic quaternary ammonium salt to transfer a nucleophile (e.g., hydr