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
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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.

 

Research of the DayEditors' Choice: Spotlights

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Radical Chlorination with Hypervalent Iodine(III) Generated by Ligand Exchange: Revisiting Palladium(II)-Catalyzed Directed C-H Chlorination

Radical Chlorination with Hypervalent Iodine(III) Generated by Ligand Exchange: Revisiting Palladium(II)-Catalyzed Directed C-H Chlorination

Chlorination revisited: A radical chlorine species, generated by ligand exchange in hypervalent iodine(III) compounds, is demonstrated to promote Pd-catalyzed directed C-H chlorination. In this protocol, ammonium salts are used as chlorine sources.

[Communication]
Kyungjun Kang, Suyeon Lee, Hyunwoo Kim
Asian J. Org. Chem., Jan 30, 2015, DOI: 10.1002/ajoc.201402284. Read article.

Palladium-Catalyzed Oxidative C-C Bond Cleavage of α-Hydroxyketones: Application to C-H Acylation of Azoarenes and Synthesis of a Liver(X) Receptor Agonist

Palladium-Catalyzed Oxidative C-C Bond Cleavage of α-Hydroxyketones: Application to C-H Acylation of Azoarenes and Synthesis of a Liver(X) Receptor Agonist

Soul acyl-um: Palladium-catalyzed oxidative C-C cleavage of α-hydroxyketones and 2-aryl acetophenones in the presence of tert-butyl hydrogen peroxide (TBHP) and subsequent C-H acylation of azoarenes with the generated acyl moiety provides easy access to acyl azoarenes.

[Full Paper]
Biju Majhi, Sabir Ahammed, Debasish Kundu, Brindaban C. Ranu
Asian J. Org. Chem., Jan 30, 2015, DOI: 10.1002/ajoc.201402280. Read article.