Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Sara Stas"'
Autor:
Sara Stashluk, Michelle Ramos, Tyla Carettini, James B. Cutrell, Seana Mathew, Marguerite Monogue, Jennifer Nguyen, James M. Sanders, Esther Y. Golnabi
Publikováno v:
Antimicrobial Stewardship & Healthcare Epidemiology, Vol 4 (2024)
Abstract Purpose: Pharmacist-led initiatives providing optimization of medications during transitions of care (TOC) have shown to have a positive impact on prescribing practices and patient outcomes. This study aims to evaluate the role and impact o
Externí odkaz:
https://doaj.org/article/356305c24172433eb579d5e999c6206a
Autor:
Jérôme Cornil, Jean-Yves Balandier, Yves Geerts, Vincent Lemaur, Franco Cacialli, Giulia Tregnago, Florence Quist, Oliver Fenwick, Sara Stas
Publikováno v:
Dyes and Pigments. 97:198-208
Synthesis, isolation and characterization of diketopyrrolopyrrole (DPP) dimers are described. These derivatives were prepared starting from symmetric or asymmetric DPP monomers through Pd-catalyzed homocoupling, Yamamoto coupling or Suzuki coupling.
Autor:
Antoine Van Vooren, Jean-Yves Balandier, Maud Jenart, Jérôme Cornil, Julie Leroy, Yves Geerts, Claude Niebel, Alix Mignolet, Sara Stas
Publikováno v:
Tetrahedron. 68:349-355
Two quaterthiophene-based dimers including an ethylene bridge have been designed and efficiently prepared; experimental and computational studies show a promising potential as semiconducting material with a charge transport of higher dimensionality c
Autor:
Jean-Yves Balandier, Pol Boudard, Yves Geerts, Sara Stas, Vincent Lemaur, Florence Quist, Benoît Tylleman, Claude Niebel, Jérôme Cornil, Roberto Lazzaroni, Noham Sebaihi
Publikováno v:
European Journal of Organic Chemistry, 17
European Journal of Organic Chemistry
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2011, 2011 (17), pp.3131-3136
European Journal of Organic Chemistry
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2011, 2011 (17), pp.3131-3136
The synthesis and characterization of two new anthradithiophene (ADT) derivatives substituted by thiophenyl or 2-octylthiophenyl units at the 5,11-positions and donor (triphenylamine) or acceptor (aldehyde functions) moieties at the 2,8-positions of
Autor:
Martin Havlík, Sergey Sergeyev, Bohumil Dolenský, Jan Čejka, Sara Stas, Christophe M. L. Vande Velde, Adrienne Remacle, Vladimír Král
Publikováno v:
Tetrahedron: asymmetry
The separation of enantiomers of several ‘bis- and tris-Troger’s bases’ by HPLC on commercially available chiral stationary phase Whelk O1 is described for the first time. The observed structure–enantioselectivity relationships are in agreeme
Publikováno v:
Tetrahedron. 65:1957-1966
β,β-Dihalo- and β,β,β-trichloroamines, obtained by Lewis acid-promoted Petasis-type reaction of α,α-dichlorinated and α,α,α-trichlorinated imines or reduction of α,α-dihaloaldimines, were subjected to a reactivity study and turned out to
Publikováno v:
Tetrahedron. 64:3457-3463
Potassium alkynyltrifluoroborates and potassium (2-phenyl)vinyltrifluoroborates react with N-3-butenyl-(2,2-dichloro-1-propylidene)amine in the presence of BF3·Et2O as a Lewis acid to synthesize rearranged Mannich products. The reaction starts with
Autor:
Sara Stas, Kourosch Abbaspour Tehrani
Publikováno v:
Tetrahedron. 63:8921-8931
Potassium phenylethynyltrifluoroborate and potassium styryltrifluoroborates react with α,α-dichlorinated aldimines in the presence of BF 3 ·OEt 2 as a Lewis acid to give a new stable class of functionalized propargylamines and allylamines. The use
Publikováno v:
ChemInform. 45
A wide variety of allylic amines from imines and alkynes are synthesized by using In(O-Tf)3 as Lewis acid.
Publikováno v:
Chemistry: a European journal
A variety of N-alkyl-α,α-dichloroaldimines were vinylated by terminal acetylenes in the presence of Lewis acids such as In(OTf)3 or BF3⋅OEt2 and hexafluoroisopropanol (HFIP) as an additive. The reaction proceeds at ambient temperature and leads t