ChemPubSoc Europe is an organization of 16 European chemical societies, founded in the late 1990s as a consequence of the amalgamation of many chemical journals owned by national chemical societies into a number of high-quality European journals.
ChemPubSoc Europe's journals, all published with Wiley-VCH, are: Chemistry—A European Journal, European Journal of Organic Chemistry, European Journal of Inorganic Chemistry, ChemBioChem, ChemPhysChem, ChemMedChem, ChemSusChem, ChemCatChem, ChemPlusChem, ChemElectroChem, ChemistryOpen, and ChemViews, the ChemPubSoc Europe e-zine. They replaced 16 traditional national chemistry journals.
The participating societies share a commitment to scientific excellence, to publishing ethics, and to the highest standards in publication, which are the basis for the success of the ChemPubSoc Europe journals.
ChemPubSoc Europe and its Asian sister organization, the Asian Chemical Editorial Society (ACES), mutually support each other in the publication of their journals Chemistry—A European Journal, Chemistry—An Asian Journal, and ChemSusChem.
© Wiley-VCH 2009–2013
The latest impact factors for the ChemPubSoc Europe journals are as follows (2013):
|Chemistry A—European Journal||5.696|
|European Journal of Organic / Inorganic Chemistry||3.145 / 2.965|
|ChemPhysChem / ChemElectroChem||3.360 / n/a|
|ChemBioChem / ChemMedChem||3.060 / 3.046|
|ChemSusChem / ChemCatChem||7.117 / 5.044|
|ChemPlusChem / ChemistryOpen||3.242 / 2.938|
Bicyclic silyl ether derivative 1a, which is easily prepared from trans-4-L-hydroxyproline, is much more stable toward protodesilylation than Jørgensen–Hayashi's catalyst 2a. Despite their structural analogy, 1a behaves as a very efficient catalyst in iminium chemistry, but is much less active than 2a in the enamine activation mode. Here, 1a exhibits a higher or equivalent level of stereocontrol.
Marco Lombardo, Lucia Cerisoli, Elisabetta Manoni, Elisa Montroni, Arianna Quintavalla, Claudio Trombini
Eur. J. Org. Chem., Aug 19, 2014, DOI: 10.1002/ejoc.201402732. Read article.
The crystal structure of [(η5-C5H4–COOH)Mo(CO)2(η3-C3H5)] (1) is presented. Both 1 and its phenylalanine derivative were included into β-cyclodextrin (CD) and per-O-methylated β-CD (TRIMEB). Overall, the inclusion contributed to a higher and more specific action on tumour cells, thereby lowering deleterious effects on a healthy myoblast line.
Susana S. Braga, Vijaya Mokal, Filipe A. Almeida Paz, Martyn Pillinger, Ana F. Branco, Vilma A. Sardão, Cátia V. Diogo, Paulo J. Oliveira, Maria P. M. Marques, Carlos C. Romão, Isabel S. Gonçalves
Eur. J. Inorg. Chem., Aug 19, 2014, DOI: 10.1002/ejic.201402540. Read article.