Mission Statement

The Asian Chemical Editorial Society (ACES) is an organization of 13 major chemical societies in Asia and the Pacific. It was founded in 2005 as a conglomeration of chemical societies with the mutual aim of creating a modern publishing forum for research in Asia and coordinating future publishing activities.

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 Chemistry—An Asian Journal and its associated journals.

Publications

Chemistry—An Asian Journal

A sister journal of Angewandte Chemie and Chemistry—A European Journal

Supporting Organizations: ChemPubSoc Europe, Gesellschaft Deutscher Chemiker (German Chemical Society, GDCh), Federation of Asian Chemical Societies (FACS).

Asian Journal of Organic Chemistry

A sister journal of the European Journal of Organic Chemistry

For the publication of the AsianJOC, ACES is joined by the Korean Society of Organic Synthesis.

Supporting Organization: ChemPubSoc Europe

ACES supports the publication of the ChemPubSoc Europe journals Chemistry—A European Journal, the European Journal of Organic Chemistry, and ChemSusChem.

© Wiley-VCH 2012

Journals

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Chem Asian J

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ChemAsianJ for iPad

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Asian J Org Chem

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AsianJOC for iPad

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ChemNanoMat

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Sister
Journals

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Angew Chem

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Chem Eur J

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Eur J Org Chem

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Associated
Journal

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ChemSusChem

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Related
Journals

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Chem Rec

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Chin J Chem

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J Chin Chem Soc

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News

Editorials: New Developments

Chemistry - An Asian Journal Theresa Kueckmann
A Reason to Celebrate!
Chem. Asian J. 2015 10, 4.

Asian Journal of Organic ChemistryRichard Threlfall
Something Old, Something New, Something Borrowed, Something Blue
Asian J. Org. Chem. 2015 4, 4.

Asian Journal of Organic ChemistryTheresa Kueckmann, Claire Cobley
ChemNanoMat—A New Journal for Small Science with a Big Impact
ChemNanoMat 2015 DOI: 10.1002/cnma.201500007.

 

Research of the DayEditors' Choice: Spotlights

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Silver-Nitrite-Assisted In Situ Diazotization Reaction: Cross-Coupling of Anilines with Arylboronic Acids at Room Temperature

Silver-Nitrite-Assisted In Situ Diazotization Reaction: Cross-Coupling of Anilines with Arylboronic Acids at Room Temperature

More than a silver lining: A silver-nitrite-assisted, in situ, diazotization reaction for the Pd-catalyzed coupling of anilines and arylboronic acids is demonstrated at room temperature under base-, additive-, and ligand-free conditions. The protocol tolerates a variety of functional groups such as nitro, ester, trifluoromethyl, trifluoromethylether, thioether, methoxy, tert-butyl, and halogen.

[Communication]
Saravanan Gowrisankar, Jayasree Seayad
Asian J. Org. Chem., Mar 25, 2015, DOI: 10.1002/ajoc.201500063. Read article.