Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Michael Parmentier"'
Autor:
Arndt Meyer, Daniel Baeschlin, Cara E. Brocklehurst, Myriam Duckely, Fabrice Gallou, Lucie E. Lovelle, Michael Parmentier, Thierry Schlama, Radka Snajdrova, Yves P. Auberson
Publikováno v:
CHIMIA, Vol 75, Iss 11, Pp 936-942 (2021)
We present a short overview of the way Novartis chemists interact and collaborate with the academic chemistry community in Switzerland. This article exemplifies a number of collaborations, and illustrates opportunities to foster research synergies be
Externí odkaz:
https://doaj.org/article/0be771cd20a34e51afe795c8508edda4
Autor:
Vincent Debrauwer, Ivo Leito, Märt Lõkov, Sofja Tshepelevitsh, Michael Parmentier, Nicolas Blanchard, Vincent Bizet
Publikováno v:
ACS Organic & Inorganic Au, Vol 1, Iss 2, Pp 43-50 (2021)
Externí odkaz:
https://doaj.org/article/0222b55685594273b741a8ea50a903c4
Publikováno v:
Frontiers in Psychology, Vol 12 (2021)
Aim: Longitudinal studies are rare in the field of writing research, and little is known about the concurrent development of the two transcription skills: spelling and handwriting. This study was designed to provide a comprehensive picture of the dev
Externí odkaz:
https://doaj.org/article/d2b17a0bf0494e68bd27d7a25272c3c3
Autor:
Margery Cortes-Clerget, Nnamdi Akporji, Jianguang Zhou, Feng Gao, Pengfei Guo, Michael Parmentier, Fabrice Gallou, Jean-Yves Berthon, Bruce H. Lipshutz
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
Chemo-enzymatic tandem processes allow access to more complex non-racemic products. Here, the authors show that non-ionic surfactants, especially the tailor-made surfactant TPGS-750-M, enhance the activity of alcohol dehydrogenase to afford stereopur
Externí odkaz:
https://doaj.org/article/2324756d621441b68c4e51ade06bad80
Publikováno v:
CHIMIA, Vol 73, Iss 9 (2019)
Mimicking an enzyme's exquisite activity and selectivity is a long-standing goal for sustainable chemical method development in aqueous media. The use of interface-rich aqueous systems, such as single-chain polymers, micelles and vesicle membranes re
Externí odkaz:
https://doaj.org/article/26872e280e0949d58c64bd14e93c22d8
Autor:
Fabrice Gallou, Michael Parmentier
Publikováno v:
Encyclopedia of Reagents for Organic Synthesis. :1-9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdf108cda266c87334eaad221c6efb02
https://doi.org/10.1002/047084289x.rn02376
https://doi.org/10.1002/047084289x.rn02376
Publikováno v:
Angewandte Chemie (International Ed. in English)
Vicinal aminoalcohols are widespread structural motifs in bioactive molecules. We report the development of a new dioxazolone reagent containing a p‐nitrophenyldifluoromethyl group, which 1. displays a good safety profile; 2. shows a remarkably hig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::321fb17528389cde44a01120213c380d
https://doi.org/10.1002/anie.202110019
https://doi.org/10.1002/anie.202110019
Autor:
Robert Schreiber, Hajar Baguia, Adrian Clarke, Stephane Rodde, Michael Parmentier, Fabrice Gallou, Lukas Hueber, Ruedi Haenggi, Xiaoming Zheng, Christoph Krell, Luca Sciascera
Publikováno v:
Organic Process Research & Development. 25:900-915
The implications of the use of surfactant TPGS-750-M in water as a micellar reaction medium on the concomitant aqueous waste streams and their sustainable disposal have been studied. Biodegradabili...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a5c665a6cc2f253a2be740e2e6edba8
https://doi.org/10.1021/acs.oprd.0c00547
https://doi.org/10.1021/acs.oprd.0c00547
Autor:
Charlotte Dalton, Louis J. Diorazio, Jaika Doerfler, Oliver D. Engl, Zhengxu S. Han, Gareth P. Howell, Jonathan Latham, Wei Li, Mark McLaws, Rachel H. Munday, Antonio Navarro, Michael Parmentier, Jan Pawlas, Paul Richardson, Gheorghe-Doru Roiban, Alan Steven, Jack A. Terrett, Daniel S. Treitler, Mingshuo Zeng
Publikováno v:
Organic Process Research & Development. 25:703-712
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0c4e78405e7f843c43041b651477123
https://doi.org/10.1021/acs.oprd.1c00067
https://doi.org/10.1021/acs.oprd.1c00067
Autor:
Margery Cortes-Clerget, Xiaobin Ge, Fabrice Gallou, Kangming Zhao, Bin Wu, Ning Ye, Lei Shi, Morgan Louis Regnier, Yu Zheng, Michael Parmentier, Xiaodong Shen
Publikováno v:
Chemical Communications. 57:7629-7632
A robust and sustainable C(sp2)–C(sp3) cross-electrophile coupling was developed via nickel/copper synergistic catalysis under micellar conditions. This protocol provided a general method to access alkylated arenes with good to excellent yields on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1534cb9964c0907622ab3c0f9476944f
https://doi.org/10.1039/d1cc02885e
https://doi.org/10.1039/d1cc02885e