Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Editor: Michael Rowan; Editorial Board Chairs: Uwe Bornscheuer, Luis A. Oro, Bert Weckhuysen
Impact Factor: 5.044
ISI Journal Citation Reports © Ranking: 2013: 26/136 (Chemistry Physical)
Online ISSN: 1867-3899
February 01, 2014
New Online Manuscript Submission System
We are pleased to announce that after over ten years, manuscriptXpress was replaced by a new Manuscript handling system, EditorialManager from ARIES, on February 1.
The links to the new journal sites are available at: chemistryviews.org/submission.
Articles that have been submitted to manuscriptXpress will be processed from there.
Thank you for your patience and we look forward to receiving your next excellent manuscript.
Recently Published Articles
- Enzymatic Synthesis of a Key Intermediate for Rosuvastatin by Nitrilase-Catalyzed Hydrolysis of Ethyl (R)-4-Cyano-3-hydroxybutyate at High Substrate Concentration
Dr. Peiyuan Yao, Jianjiong Li, Jing Yuan, Chao Han, Xiangtao Liu, Prof. Jinhui Feng, Prof. Qiaqing Wu and Prof. Dunming Zhu
Article first published online: 25 NOV 2014 | DOI: 10.1002/cctc.201402877
Old enzyme, new tricks: An efficient hydrolysis of ethyl (R)-4-cyano-3-hydroxybutyate to ethyl (R)-3-hydroxyglutarate by a known nitrilase from Arabidopsis thaliana (AtNIT2) has been developed. High substrate concentration, high chemoselectivity, and high yield are obtained by using free and immobilized whole cells.
- Magnetically Recoverable Palladium(0) Nanocomposite Catalyst for Hydrogenation Reactions in Water
Dr. Carl-Hugo Pélisson, Dr. Audrey Denicourt-Nowicki, Cristelle Meriadec, Dr. Jean-Marc Greneche and Prof. Alain Roucoux
Article first published online: 25 NOV 2014 | DOI: 10.1002/cctc.201402761
Active, selective, and reusable! A magnetically Pd0 nanocomposite was easily prepared and efficiently used in hydrogenation reactions of various substrates (nitro- and/or halogenoarenes) in neat water.
- Asymmetric Organocatalyzed Epoxidation of 2-Oxoindoline-3-ylidene Acetaldehydes
Takasuke Mukaiyama, Kento Ogata, Tsuyoshi Ono and Prof. Yujiro Hayashi
Article first published online: 24 NOV 2014 | DOI: 10.1002/cctc.201402811
Giving metal catalysis the slip: The asymmetric epoxidation of 2-oxoindoline-3-ylidene acetaldehydes with hydrogen peroxide, catalyzed by diarylprolinol silyl ether, has been developed. Good to excellent diastereo- and enantioselectivities were realized even though the starting material 2-oxoindoline-3-ylidene acetaldehydes pre-existed as a mixture of E/Z-isomers.
- A New Role for Sulfenate Anions: Organocatalysis
Prof. Dr. Adrian L. Schwan
Article first published online: 24 NOV 2014 | DOI: 10.1002/cctc.201402817
Introducing…Sulfenate! The sulfenate anion is introduced for the first time as a catalyst and was found to facilitate the conversion of benzyl halides to trans-stilbenes. CPME=Cyclopentyl methyl ether.
- Recycling Powered by Release of Carbon Dioxide
Anna Laurell Nash, Dr. Khalid Widyan and Prof. Christina Moberg
Article first published online: 19 NOV 2014 | DOI: 10.1002/cctc.201402765
A carbon dioxide tap: In a cyclic process, fed with external chemical energy generated by the transformation of a compound with high chemical potential to carbon dioxide, the undesired enantiomer from a catalytic asymmetric reaction is continuously recycled to the starting reagent. This minor enantiomer recycling is characterized by gradually increasing yields and product enantiomeric ratios.