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
- The Hydrogenation of Aromatic Compounds under Mild Conditions by Using a Solid Lewis Acid and Supported Palladium Catalyst
Peng Zhang, Tianbin Wu, Minqiang Hou, Jun Ma, Huizhen Liu, Tao Jiang, Weitao Wang, Congyi Wu and Prof. Buxing Han
Article first published online: 21 OCT 2014 | DOI: 10.1002/cctc.201402671
Hydroxyl groups hold the key: Al2O3 or SiO2 particles with abundant surface hydroxyl groups can prevent side reactions of aromatic compounds with AlCl3 completely; in the absence of these solid oxide particles the aromatic compounds tested undergo dehydrogenation condensation. This catalytic system has been successfully utilized in the highly efficient hydrogenation of aromatic compounds under mild conditions by using AlCl3–Pd/Al2O3 or AlCl3–Pd/SiO2 catalysts.
- Synthesis of Quinoxalines by a Carbon Nanotube–Gold Nanohybrid-Catalyzed Cascade Reaction of Vicinal Diols and Keto Alcohols with Diamines
Dr. Nimesh Shah, Dr. Edmond Gravel, Dr. Dhanaji V. Jawale, Dr. Eric Doris and Prof. Dr. Irishi N. N. Namboothiri
Article first published online: 21 OCT 2014 | DOI: 10.1002/cctc.201402782
Mild and free: A one-pot oxidation–condensation method for the synthesis of quinoxalines from readily available benzoins or benzhydrols and aromatic 1,2-diamines is achieved by use of a gold–carbon nanotube nanohybrid. Quinoxalines are formed under mild conditions in air and in excellent yields.
- Lipase-Catalyzed Doubly Enantioselective Ring-Opening Resolution between Alcohols and Lactones: Synthesis of Chiral Hydroxyl Esters with Two Stereogenic Centers
Dr. Bo Xia, Yanyan Li, Dr. Guilin Cheng, Prof. Xianfu Lin and Dr. Qi Wu
Article first published online: 21 OCT 2014 | DOI: 10.1002/cctc.201402672
Opening new doors: A novel lipase B from Candida antarctica-catalyzed doubly enantioselective ring-opening resolution between racemic alcohols and lactones is developed.
- Synthesis of Amines by Reductive Amination of Aldehydes and Ketones using Co3O4/NGr@C Catalyst
Sabine Pisiewicz, Tobias Stemmler, Dr. Annette-Enrica Surkus, Dr. Kathrin Junge and Prof. Dr. Matthias Beller
Article first published online: 21 OCT 2014 | DOI: 10.1002/cctc.201402527
A cobalt from the blue: Heterogenized cobalt oxide-based catalysts (Co3O4/NGr@C) allow for reductive aminations of aldehydes and ketones. Diverse carbonyl compounds were transformed with secondary amines to the corresponding tertiary amines with moderate to high yields in good selectivity. The Co3O4/NGr@C catalyst was recycled up to five times without significant loss of activity.
- Exploring the Reactivity of Nickel Pincer Complexes in the Decomposition of Formic Acid to CO2/H2 and the Hydrogenation of NaHCO3 to HCOONa
Dr. Stephan Enthaler, Dr. Andreas Brück, Anja Kammer, Dr. Henrik Junge, Dr. Elisabeth Irran and Dr. Samet Gülak
Article first published online: 19 OCT 2014 | DOI: 10.1002/cctc.201402716
A nickel for your hydrogen economy: The catalytic abilities of nickel complexes modified by a PCP pincer ligand in the decomposition of formic acid to produce dihydrogen and carbon dioxide have been studied.