Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Scott R. Perrin"'
Publikováno v:
Separations Technology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e762e964707841461667e7752eaaf291
https://doi.org/10.1201/9780367813321-5
https://doi.org/10.1201/9780367813321-5
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6949896cf55cd29041a1ce78a93c39a0
https://doi.org/10.1021/op700118m
https://doi.org/10.1021/op700118m
Publikováno v:
Journal of Chromatography A. 758:93-98
The Whelk-O 1 chiral stationary phase is generally useful for the chromatographic separation of the enantiomers of many classes of analytes including aryl propionic acid non-steroidal anti-inflammatory drugs, aryl epoxides, sulfoxides, alcohols, amid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aacd54698a3516ebd031284d9c986cf6
https://doi.org/10.1016/s0021-9673(96)00569-9
https://doi.org/10.1016/s0021-9673(96)00569-9
Autor:
Scott R. Perrin, Christopher J. Welch
Publikováno v:
Journal of Chromatography A. 690:218-225
The previously described α-Burke 1 chiral stationary phase (CSP) was designed for the chromatographic separation of the enantiomers of s-blockers. Difficulties with the reproducibility of the free radical addition reaction, used in the attachment of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1aea99b41b5e0714d1a14fe8751ef29d
https://doi.org/10.1016/0021-9673(94)01143-3
https://doi.org/10.1016/0021-9673(94)01143-3
Synthesis, absolute configuration, and analysis of malathion, malaoxon, and isomalathion enantiomers
Publikováno v:
Chemical Research in Toxicology. 6:718-723
Syntheses of the enantiomers of malathion, malaoxon, and isomalathion are reported herein. Malathion enantiomers were prepared from (R)- or (S)-malic acid in three steps. Enantiomers of malathion were converted to the corresponding enantiomers of mal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3913140a54c5706154a69e48dfc8f443
https://doi.org/10.1021/tx00035a018
https://doi.org/10.1021/tx00035a018
Autor:
Scott R. Perrin
Publikováno v:
Chirality. 3:188-195
A Pirkle-concept chiral stationary phase (CSP) derived from N-(1-naphthyl)leucine was evaluated for developing methods to reduce analysis times and investigating techniques in the rapid screening of a variety of chiral compounds over a given chiral s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4ddebedc73dbffd43f27a893a90c769
https://doi.org/10.1002/chir.530030309
https://doi.org/10.1002/chir.530030309
Publikováno v:
Journal of High Resolution Chromatography. 20:179-180
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e88ef6cceb7055141d6b8337ac8f9d19
https://doi.org/10.1002/jhrc.1240200311
https://doi.org/10.1002/jhrc.1240200311
Autor:
Scott R. Perrin, Wilhelm Hauck, Elias Ndzie, Jean Blehaut, Olivier Ludemann-Hombouger, Roger-Marc Nicoud, William H. Pirkle
Publikováno v:
Organic Process Research & Development; Aug2007, Vol. 11 Issue 5, p817-824, 8p