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the Altmetric Attention Score and how the score is calculated. Search for more papers by this author. Primary alcohols are readily decarbonylated even at room temperature to give catalytically inactive 16e Ir–CO adducts. it in a third party non-RSC publication you must
Get article recommendations from ACS based on references in your Mendeley library. Learn about our remote access options, Leibniz-Institut für Katalyse e.V. Monica Trincado, Dipshikha Banerjee, Hansjörg Grützmacher. What is catalytic dehydrogenation of alcohol? Zheng Wang, Bing Pan, Qingbin Liu, Erlin Yue, Gregory A. Solan, Yanping Ma, Wen-Hua Sun. Unlimited viewing of the article PDF and any associated supplements and figures. Go to our
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If you do not receive an email within 10 minutes, your email address may not be registered, For permission to reproduce, republish and Pardeep Dahiya. 7-6-7 Ring-based transition-metal catalysts for the transfer dehydrogenation of isopropanol. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Dehydrogenation of Secondary Alcohols with Reduced Copper. system. not otherwise permitted to reproduce, republish, redistribute, or sell any Supporting Information Svenja Budweg, Kathrin Junge, Matthias Beller. Iridium-catalysed dehydrocoupling of aryl phosphine–borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes). Information about how to use the RightsLink permission system can be found at Catalytic Dehydrogenation of Isopropyl Alcohol (Part 1). redistribute this material, requesters must process their own requests via the RightsLink permission Cp*Co III ‐Catalyzed Efficient Dehydrogenation of Secondary Alcohols Dr. Manoj Kumar Gangwar. Please check your email for instructions on resetting your password. Multiple C–H activations in an iridium pincer complex. Learn more. Information about reproducing material from RSC articles with different licences
Irene Mellone, Nikolaus Gorgas, Federica Bertini, Maurizio Peruzzini, Karl Kirchner, and Luca Gonsalvi . Iridium Pincer Complexes with an Olefin Backbone. h
http://pubs.acs.org/page/copyright/permissions.html, https://doi.org/10.1021/acs.chemrev.6b00556, https://doi.org/10.1021/acs.organomet.6b00846, https://doi.org/10.1021/acs.organomet.6b00598, https://doi.org/10.1021/acs.organomet.6b00551, https://doi.org/10.1021/acs.organomet.6b00607, https://doi.org/10.1021/acs.organomet.6b00085, https://doi.org/10.1021/acs.organomet.5b00743, https://doi.org/10.1021/acs.inorgchem.5b01428, https://doi.org/10.1021/acs.organomet.5b00495, https://doi.org/10.1021/acs.organomet.5b00496, https://doi.org/10.1016/j.cattod.2020.10.022, https://doi.org/10.1007/s11172-018-2067-x, https://doi.org/10.1007/s11172-018-2033-7, https://doi.org/10.1016/j.jorganchem.2017.05.018, https://doi.org/10.1016/j.jorganchem.2015.08.008, https://doi.org/10.1080/10426507.2015.1012669, https://doi.org/10.1016/bs.adomc.2015.02.004. ) catalyst. N -alkylation of amines with secondary alcohols here it is. 2
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thanks for a2a tc iii Cp*Co( Fine Chemicla Laboratory, Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur, Uttar Pradesh, 208 016 India . Molecular catalysts for hydrogen production from alcohols. Toni T. Metsänen, Peter Hrobárik, Hendrik F. T. Klare, Martin Kaupp, and Martin Oestreich .
Brian C. Gruver, Jeramie J. Adams, Navamoney Arulsamy, and Dean M. Roddick . This may take some time to load. Catalytic Dehydrogenation of Isopropyl Alcohol (Part 1). Corresponding authors, a
As a service to our authors and readers, this journal provides supporting information supplied by the authors. Answer : Dehydration of 1-methylcyclohexanol can give two products, viz, I and II. Phosphorus, Sulfur, and Silicon and the Related Elements. from the ACS website, either in whole or in part, in either machine-readable form or any other form Learn more. Please check your email for instructions on resetting your password. ii Best results are obtained using di-picolylamine derivatives as ligands and acetone as an inexpensive hydrogen acceptor. Any queries (other than missing content) should be directed to the corresponding author for the article. Find more information about Crossref citation counts. and you may need to create a new Wiley Online Library account. Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Dehydrogenation of alcohols by three iridium pincer complexes, IrH(Cl)[2,6-(tBu2PO)2C6H3] (1), {IrH(acetone)[2,6-(tBu2PO)2C6H3]}{BF4} (2), and IrH(Cl)[{2,5-(tBu2PCH2)2C5H2}Ru(C5H5)] (3), is reported, in both the presence and the absence of a sacrificial hydrogen acceptor. Understanding the reaction mechanisms of Pd-catalysed oxidation of alcohols and domino oxidation–arylation reactions using phenyl chloride as an oxidant. Pombeiro. Such materials are peer reviewed and may be re‐organized for online delivery, but are not copy‐edited or typeset. Any queries (other than missing content) should be directed to the corresponding author for the article. to access the full features of the site or access our, Leibniz-Institut für Katalyse e.V. ) tetraphosphine-based catalytic system for hydrogen production by selective formic acid dehydrogenation. Fine Chemicla Laboratory, Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur, Uttar Pradesh, 208 016 India . Number of times cited according to CrossRef: Efficient Transfer Hydrogenation of Ketones using Methanol as Liquid Organic Hydrogen Carrier. Information. You’ve supercharged your research process with ACS and Mendeley! ) complexes of a cooperative tridentate enamide-diphosphine ligand platform. Leibniz-Institut für Katalyse e.V. Acceptorless Dehydrogenative Oxidation of Secondary Alcohols Catalysed by Cp*Ir
Yuan Shi, Takuya Suguri, Satoshi Kojima, Yohsuke Yamamoto. The well‐defined iron PNP pincer complex catalyst [Fe(H)(BH4)(CO)(HN{CH2CH2P(iPr)2}2] was used for the catalytic dehydrogenation of secondary alcohols to give the corresponding ketones.
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