Mission Statement

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

Portal &
Magazine

Cover
ChemistryViews

Cover
ChemViews

Journals

Cover
Chem Eur J

Get content alert
ChemEurJ for iOS

Cover
Eur J Org Chem

Get content alert
EurJIC for iPad

Cover
Eur J Inorg Chem

Get content alert
EurJIC for iPad

Receive e-mail alerts when new issues are available online. Registration is easy, fast and free.
Learn more.

Cover
ChemPhysChem

Get content alert
ChemPhysChem for iOS

Cover
ChemBioChem

Get content alert
ChemBioChem for iPad

Cover
ChemMedChem

Get content alert
ChemMedChem for iPad

Cover
ChemSusChem

Get content alert
ChemSusChem for iPad

Cover
ChemCatChem

Get content alert
ChemCatChem for iPad

Cover
ChemPlusChem

Get content alert
ChemPlusChem for iOS

Cover
ChemElectroChem

Get content alert
ChemElectroChem for iOS

Cover
ChemistryOpen

Get content alert
ChemistryOpen for iOS

Sister
Journals

Cover
Chem Asian J

Get content alert
ChemAsianJ for iPad

Cover
Asian J Org Chem

Get content alert
AsianJOC for iPad

Cover
Angew Chem

Get content alert
Angewandte International for iPad
Angewandte fuer iPad

News

Latest Impact Factors

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

 

RSS Feed

Multicomponent Cascade Synthesis of Biaryl-Based Chalcones in Pure Water and in an Aqueous Micellar Environment

Multicomponent Cascade Synthesis of Biaryl-Based Chalcones in Pure Water and in an Aqueous Micellar Environment

The multicomponent cascade synthesis of biaryl-based chalcones was carried out in pure water and in an aqueous micellar system. The first step of the protocol was a simple Pd-catalysed, ligand-free, and aerobic Suzuki–Miyaura reaction in aqueous medium. The resulting intermediates then underwent an in-situ aldol condensation reaction to give biaryl(hetero)chalcones in good to excellent yields.

[Full Paper]
Nicola Armenise, Danilo Malferrari, Sara Ricciardulli, Paola Galletti, Emilio Tagliavini
Eur. J. Org. Chem., March 2, 2016, DOI: 10.1002/ejoc.201600095. Read article.

A Formal Intermolecular Iodolactonization Reaction Based on a Radical-Ionic Sequence

A Formal Intermolecular Iodolactonization Reaction Based on a Radical-Ionic Sequence

A radical-ionic sequence between an allylic alcohol and an α-iodo acid in the presence of substoichiometric amounts of lauroyl peroxide (DLP) produced the adduct of an atom transfer radical addition (ATRA), which underwent an acid-mediated lactonization to afford the corresponding iodolactone. This approach can be described as a formal intermolecular iodolactonization.

[Full Paper]
David F. León-Rayo, Maricela Morales-Chamorro, Alejandro Cordero-Vargas
Eur. J. Org. Chem., March 2, 2016, DOI: 10.1002/ejoc.201600051. Read article.

Selective Elaboration of Aminodiols towards Small Ring α- and β-Amino Acid Derivatives that Incorporate an Aziridine, Azetidine, or Epoxide Scaffold

Selective Elaboration of Aminodiols towards Small Ring ?- and ?-Amino Acid Derivatives that Incorporate an Aziridine, Azetidine, or Epoxide Scaffold

The dihydroxylation of N-substituted alkyl 2-(aminomethyl)acrylates afforded the corresponding 2-(aminomethyl)-2,3-dihydroxypropanoates in good yields. The resulting amino-1,2-diols were shown to be suitable substrates for the efficient synthesis (one to four steps) of small ring heterocyclic amino acid derivatives that incorporate epoxide, aziridine, or azetidine ring systems.

[Full Paper]
Elena Semina, Asta Žukauskaite, Algirdas Šačkus, Norbert De Kimpe, Sven Mangelinckx
Eur. J. Org. Chem., March 2, 2016, DOI: 10.1002/ejoc.201600036. Read article.

Isolation and Structures of 1,2,3-Triazole-Derived Mesoionic Biscarbenes with Bulky Aromatic Groups

Isolation and Structures of 1,2,3-Triazole-Derived Mesoionic Biscarbenes with Bulky Aromatic Groups

1,2,3-Triazole-derived mesoionic biscarbenes bridged by a pyridylene group are synthesized and characterized. The carbenes are thought to be partly reduced to anionic radical species in the presence of strong bases, which suggests that these moieties endow molecules with both electron-acceptor and -donor properties. A rare example of an iron complex with a pincer carbene is synthesized.

[Communication]
Haruka Iwasaki, Yuji Yamada, Ryuta Ishikawa, Yuji Koga, Kouki Matsubara
Eur. J. Org. Chem., March 2, 2016, DOI: 10.1002/ejoc.201501626. Read article.

The Original CoII Heteroscorpionates Revisited: On the EPR of Pseudotetrahedral CoII

The Original CoII Heteroscorpionates Revisited: On the EPR of Pseudotetrahedral CoII

Solution spectroscopy of a series of five (RBpx)2Co complexes is reported. A frozen solution EPR study shows that all of the complexes have MS = 3/2 ground states, and offer insight into the complex EPR of pseudotetrahedral CoII.

[Full Paper]
Robert R. Baum, William K. Myers, Samuel M. Greer, Robert M. Breece, David L. Tierney
Eur. J. Inorg. Chem., March 2, 2016, DOI: 10.1002/ejic.201501356. Read article.

Organotemplate-Free Synthesis of a High-Silica Zeolite with a TON Structure in the Absence of Zeolite Seeds

Organotemplate-Free Synthesis of a High-Silica Zeolite with a TON Structure in the Absence of Zeolite Seeds

A high-silica aluminosilicate zeolite with a TON structure designated as ZJM-4 was successfully synthesized in the absence of any organic templates and zeolite seeds. This route has efficient silica utilization, and the zeolite product has a stable tetrahedral aluminum species.

[Full Paper]
Yeqing Wang, Chenqi Zhu, Jing Qiu, Fan Jiang, Xiangju Meng, Xiong Wang, Chi Lei, Yinying Jin, Shuxiang Pan, Feng-Shou Xiao
Eur. J. Inorg. Chem., March 2, 2016, DOI: 10.1002/ejic.201501223. Read article.