Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Patrick Piras"'
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:
Patrick Piras
Publikováno v:
Chirality
Chirality, 2022, 34 (4), pp.646-666. ⟨10.1002/chir.23423⟩
Chirality, 2022, 34 (4), pp.646-666. ⟨10.1002/chir.23423⟩
International audience; In this paper, we present several new theoretical measures based on information entropy that can be used to analyze the information content of a chiral molecule. Starting from a differentiation between "chiral" and "achiral" p
Autor:
Christopher J. Welch, Patrick Piras, Edward C. Sherer, Robert P. Sheridan, Wes Schafer, Christian Roussel
Publikováno v:
Journal of Separation Science
Journal of Separation Science, 2018, 41 (6), pp.1365-1375. ⟨10.1002/jssc.201701334⟩
Journal of Separation Science, Wiley-VCH Verlag, 2018, 41 (6), pp.1365-1375. ⟨10.1002/jssc.201701334⟩
Journal of Separation Science, 2018, 41 (6), pp.1365-1375. ⟨10.1002/jssc.201701334⟩
Journal of Separation Science, Wiley-VCH Verlag, 2018, 41 (6), pp.1365-1375. ⟨10.1002/jssc.201701334⟩
International audience; Predicting whether a chiral column will be effective is a daily task for many analysts. Moreover, finding the best chiral column for separating a particular racemic compound is mostly a matter of trial and error that may take
Autor:
Christian Roussel, Dominique Lorcy, Guilhem Javierre, Nicolas Vanthuyne, Patrick Piras, Roberta Fruttero, Marion Jean, Michel Giorgi, Vesna Risso, Daniel Farran, Jean-Valère Naubron
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, 2018, 83 (15), pp.7566-7573. ⟨10.1021/acs.joc.8b01009⟩
Journal of Organic Chemistry, American Chemical Society, 2018, 83 (15), pp.7566-7573. ⟨10.1021/acs.joc.8b01009⟩
Journal of Organic Chemistry, 2018, 83 (15), pp.7566-7573. ⟨10.1021/acs.joc.8b01009⟩
Journal of Organic Chemistry, American Chemical Society, 2018, 83 (15), pp.7566-7573. ⟨10.1021/acs.joc.8b01009⟩
International audience; For the first time, chirality in (3 Z,9 Z)-1,2,5,8-dithiadiazecine-6,7(5 H,8 H)-dione series was recognized. Enantiomers of the 4,9-dimethyl-5,8-diphenyl analogue were isolated at room temperature, and their thermal stability
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f46c75a1d9591ca36c33341534f4fcf8
https://hal.science/hal-01817538/document
https://hal.science/hal-01817538/document
Autor:
Patrick Piras, Edward C. Sherer, Robert P. Sheridan, Wes Schafer, Kerstin Zawatzky, Christopher J. Welch, Christian Roussel
Publikováno v:
Journal of Chromatography A
Journal of Chromatography A, 2016, 1467, pp.206-213. ⟨10.1016/j.chroma.2016.05.066⟩
Journal of Chromatography A, Elsevier, 2016, 1467, pp.206-213. ⟨10.1016/j.chroma.2016.05.066⟩
Journal of Chromatography A, 2016, 1467, pp.206-213. ⟨10.1016/j.chroma.2016.05.066⟩
Journal of Chromatography A, Elsevier, 2016, 1467, pp.206-213. ⟨10.1016/j.chroma.2016.05.066⟩
International audience; ChirBase, a database for the chromatographic separation of enantiomers containing more than 200,000 records compiled from the literature, was used to develop quantitative structure activity models for the prediction of which c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faad88b9f2d3acefe21084d6a7a29428
https://hal.science/hal-01441913
https://hal.science/hal-01441913
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:
Separation & Purification Reviews. 37:229-301
The enantioseparation of 123 clinically used racemic drugs by supercritical fluid chromatography (SFC) on commercial chiral stationary phases (CSPs) available in 2006 is reviewed. The CSPs were briefly described in Part I of this work. The mobile pha
Publikováno v:
Journal of Planar Chromatography – Modern TLC. 18:5-12
The paper reviews the latest achievements in chiral separation by planar chromatography (PC) since 2001. The emphasis is on cellulose derivatives and, especially, microcrystalline cellulose triacetate (MCTA). A comparison is made with HPLC data retri
Publikováno v:
Journal of Physical Organic Chemistry. 16:9-15
Information theory was used to analyse and compare organic syntheses leading to the targets, daucene, longifolene and estrone. This paper expands the work of Bertz, who analysed syntheses from the complexity of molecular structures. Herein, a more co
Autor:
Patrick Piras, Cristina Suteu, Christian Roussel, Ingolf Heitmann, Mohammed Soufiaoui, Latifa Shaimi, Brice Bonnet
Publikováno v:
Chirality. 10:770-777
Chromatographic resolution of 12 derivatives in the 4a-methyl-2,3,4,4a-tetrahydro-1H-fluorene and 4a-methyl-1,2,3,4,4a,9a-hexahydrofluoren-9-one series differing by the framework around position 9 and substitution in position 6, are reported on Chira