Vote for your favorite mineral in #MinCup25! - Taenite vs. Nontronite
It's a mineral found mostly in the farthest reaches of space vs one so common an exhaustive list of localities is nigh impossible as alloy #taenite faces off against clay #nontronite.
Log InRegister
Quick Links : The Mindat ManualThe Rock H. Currier Digital LibraryMindat Newsletter [Free Download]
Home PageAbout MindatThe Mindat ManualHistory of MindatCopyright StatusWho We AreContact UsAdvertise on Mindat
Donate to MindatCorporate SponsorshipSponsor a PageSponsored PagesMindat AdvertisersAdvertise on Mindat
Learning CenterWhat is a mineral?The most common minerals on earthInformation for EducatorsMindat ArticlesThe ElementsThe Rock H. Currier Digital LibraryGeologic Time
Minerals by PropertiesMinerals by ChemistryAdvanced Locality SearchRandom MineralRandom LocalitySearch by minIDLocalities Near MeSearch ArticlesSearch GlossaryMore Search Options
Search For:
Mineral Name:
Locality Name:
Keyword(s):
 
The Mindat ManualAdd a New PhotoRate PhotosLocality Edit ReportCoordinate Completion ReportAdd Glossary Item
Mining CompaniesStatisticsUsersMineral MuseumsClubs & OrganizationsMineral Shows & EventsThe Mindat DirectoryDevice SettingsThe Mineral Quiz
Photo SearchPhoto GalleriesSearch by ColorNew Photos TodayNew Photos YesterdayMembers' Photo GalleriesPast Photo of the Day GalleryPhotography

Wu, Xiao-Feng, Anbarasan, Pazhamalai, Neumann, Helfried, Beller, Matthias (2010) Palladium-Catalyzed Carbonylative CH Activation of Heteroarenes. Angewandte Chemie, 122 (40). 7474-7477 doi:10.1002/ange.201003895

Advanced
   -   Only viewable:
Reference TypeJournal (article/letter/editorial)
TitlePalladium-Catalyzed Carbonylative CH Activation of Heteroarenes
JournalAngewandte Chemie
AuthorsWu, Xiao-FengAuthor
Anbarasan, PazhamalaiAuthor
Neumann, HelfriedAuthor
Beller, MatthiasAuthor
Year2010 (August 25)Volume122
Issue40
PublisherWiley
DOIdoi:10.1002/ange.201003895Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID7314535Long-form Identifiermindat:1:5:7314535:6
GUID0
Full ReferenceWu, Xiao-Feng, Anbarasan, Pazhamalai, Neumann, Helfried, Beller, Matthias (2010) Palladium-Catalyzed Carbonylative CH Activation of Heteroarenes. Angewandte Chemie, 122 (40). 7474-7477 doi:10.1002/ange.201003895
Plain TextWu, Xiao-Feng, Anbarasan, Pazhamalai, Neumann, Helfried, Beller, Matthias (2010) Palladium-Catalyzed Carbonylative CH Activation of Heteroarenes. Angewandte Chemie, 122 (40). 7474-7477 doi:10.1002/ange.201003895
In(2010, August) Angewandte Chemie Vol. 122 (40) Wiley

See Also

These are possibly similar items as determined by title/reference text matching only.

Wu, Xiao-Feng, Anbarasan, Pazhamalai, Neumann, Helfried, Beller, Matthias (2010) Palladium-Catalyzed Carbonylative CH Activation of Heteroarenes. Angewandte Chemie International Edition, 49 (40). 7316-7319 doi:10.1002/anie.201003895
Wu, Xiao-Feng, Neumann, Helfried, Beller, Matthias (2010) Palladium-Catalyzed Coupling Reactions: Carbonylative Heck Reactions To Give Chalcones. Angewandte Chemie, 122 (31). 5412-5416 doi:10.1002/ange.201002155
Wu, Xiao-Feng, Anbarasan, Pazhamalai, Neumann, Helfried, Beller, Matthias (2010) Vom Edelmetall zum Nobelpreis: Palladiumkatalysierte Kupplungen als Schlüsselmethode in der organischen Synthese. Angewandte Chemie, 122 (48). 9231-9234 doi:10.1002/ange.201006374
Anbarasan, Pazhamalai, Neumann, Helfried, Beller, Matthias (2010) Efficient Synthesis of Aryl Fluorides. Angewandte Chemie, 122 (12). 2265-2268 doi:10.1002/ange.200905855
Wu, Xiao-Feng, Anbarasan, Pazhamalai, Neumann, Helfried, Beller, Matthias (2010) From Noble Metal to Nobel Prize: Palladium-Catalyzed Coupling Reactions as Key Methods in Organic Synthesis. Angewandte Chemie International Edition, 49 (48). 9047-9050 doi:10.1002/anie.201006374
Wu, Xiao-Feng, Neumann, Helfried, Beller, Matthias (2011) Convenient and General Palladium-Catalyzed Carbonylative Sonogashira Coupling of Aryl Amines. Angewandte Chemie, 123 (47). 11338-11342 doi:10.1002/ange.201104653
Wu, Xiao-Feng, Neumann, Helfried, Beller, Matthias (2010) Palladium-Catalyzed Coupling Reactions: Carbonylative Heck Reactions To Give Chalcones. Angewandte Chemie International Edition, 49 (31). 5284-5288 doi:10.1002/anie.201002155
Anbarasan, Pazhamalai, Neumann, Helfried, Beller, Matthias (2011) A General Rhodium-Catalyzed Cyanation of Aryl and Alkenyl Boronic Acids. Angewandte Chemie, 123 (2). 539-542 doi:10.1002/ange.201006044
Wu, Xiao-Feng, Neumann, Helfried, Beller, Matthias (2011) Convenient and General Palladium-Catalyzed Carbonylative Sonogashira Coupling of Aryl Amines. Angewandte Chemie International Edition, 50 (47). 11142-11146 doi:10.1002/anie.201104653
He, Lin, Li, Haoquan, Neumann, Helfried, Beller, Matthias, Wu, Xiao-Feng (2014) Highly Efficient Four-Component Synthesis of 4(3H)-Quinazolinones: Palladium-Catalyzed Carbonylative Coupling Reactions. Angewandte Chemie, 126 (5). 1444-1448 doi:10.1002/ange.201308756
Anbarasan, Pazhamalai, Neumann, Helfried, Beller, Matthias (2010) Efficient Synthesis of Aryl Fluorides. Angewandte Chemie International Edition, 49 (12). 2219-2222 doi:10.1002/anie.200905855
 
and/or  
Mindat.org is an outreach project of the Hudson Institute of Mineralogy, a 501(c)(3) not-for-profit organization.
Copyright © mindat.org and the Hudson Institute of Mineralogy 1993-2025, except where stated. Most political location boundaries are © OpenStreetMap contributors. Mindat.org relies on the contributions of thousands of members and supporters. Founded in 2000 by Jolyon Ralph.
To cite: Ralph, J., Von Bargen, D., Martynov, P., Zhang, J., Que, X., Prabhu, A., Morrison, S. M., Li, W., Chen, W., & Ma, X. (2025). Mindat.org: The open access mineralogy database to accelerate data-intensive geoscience research. American Mineralogist, 110(6), 833–844. doi:10.2138/am-2024-9486.
Privacy Policy - Terms & Conditions - Contact Us / DMCA issues - Report a bug/vulnerability Current server date and time: September 15, 2025 17:53:00
Go to top of page