Vote for your favorite mineral in #MinCup25! - Carpathite vs. Tugtupite
Battle of mineralogical oddities as organic mineral #carpathite battles against vs #tugtupite, a mineral that looks like reindeer blood!
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

Matsuda, Yuki, Tsuji, Yasushi, Fujihara, Tetsuaki (2020) Cu-Catalyzed three-component coupling reactions using nitriles, 1,3-dienes and silylboranes. Chemical Communications, 56 (34) 4648-4651 doi:10.1039/d0cc01803a

Advanced
   -   Only viewable:
Reference TypeJournal (article/letter/editorial)
TitleCu-Catalyzed three-component coupling reactions using nitriles, 1,3-dienes and silylboranes
JournalChemical Communications
AuthorsMatsuda, YukiAuthor
Tsuji, YasushiAuthor
Fujihara, TetsuakiAuthor
Year2020Volume56
Issue34
PublisherRoyal Society of Chemistry (RSC)
DOIdoi:10.1039/d0cc01803aSearch in ResearchGate
Generate Citation Formats
Mindat Ref. ID15469813Long-form Identifiermindat:1:5:15469813:3
GUID0
Full ReferenceMatsuda, Yuki, Tsuji, Yasushi, Fujihara, Tetsuaki (2020) Cu-Catalyzed three-component coupling reactions using nitriles, 1,3-dienes and silylboranes. Chemical Communications, 56 (34) 4648-4651 doi:10.1039/d0cc01803a
Plain TextMatsuda, Yuki, Tsuji, Yasushi, Fujihara, Tetsuaki (2020) Cu-Catalyzed three-component coupling reactions using nitriles, 1,3-dienes and silylboranes. Chemical Communications, 56 (34) 4648-4651 doi:10.1039/d0cc01803a
In(2020) Chemical Communications Vol. 56 (34) Royal Society of Chemistry (RSC)

See Also

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

Tanji, Yutaka, Hamaguchi, Ryo, Tsuji, Yasushi, Fujihara, Tetsuaki (2020) Pd-Catalyzed intermolecular C–H bond arylation reactions: effect of bulkiness of carboxylate ligands. Chemical Communications, 56 (27) 3843-3846 doi:10.1039/d0cc01129k
Fujihara, Tetsuaki, Yokota, Ken, Terao, Jun, Tsuji, Yasushi (2017) Copper-catalyzed hydroallylation of allenes employing hydrosilanes and allyl chlorides. Chemical Communications, 53 (56). 7898-7900 doi:10.1039/c7cc02816d
Fujihara, Tetsuaki, Tomike, Yoshikazu, Ohtake, Toshiyuki, Terao, Jun, Tsuji, Yasushi (2011) Ruthenium-catalyzed ring-closing metathesis accelerated by long-range steric effect. Chemical Communications, 47 (34). 9699pp. doi:10.1039/c1cc13304g
Obora, Yasushi, Tsuji, Yasushi, Kawamura, Takashi (1995) 1,4-Carbosilylation of 1,3-Dienes via Palladium Catalyzed Three-Component Coupling Reaction. Journal Of The American Chemical Society, 117 (39) 9814-9821 doi:10.1021/ja00144a005
Chiba, Yusuke, Oka, Yuki, Masai, Hiroshi, Matsuda, Wakana, Fujihara, Tetsuaki, Tsuji, Yasushi, Terao, Jun (2019) Two-step template method for synthesis of axis-length-controlled porphyrin-containing hollow structures. Chemical Communications, 55 (47). 6755-6758 doi:10.1039/c9cc02866h
Semba, Kazuhiko, Shinomiya, Masataka, Fujihara, Tetsuaki, Terao, Jun, Tsuji, Yasushi (2013) Highly Selective Copper-Catalyzed Hydroboration of Allenes and 1,3-Dienes. Chemistry - A European Journal, 19 (22). 7125-7132 doi:10.1002/chem.201300443
Tani, Yosuke, Yamaguchi, Tatsuya, Fujihara, Tetsuaki, Terao, Jun, Tsuji, Yasushi (2015) Copper-catalyzed Silylative Allylation of Ketones and Aldehydes Employing Allenes and Silylboranes. Chemistry Letters, 44 (3). 271-273 doi:10.1246/cl.141018
Fujihara, Tetsuaki, Tani, Yosuke, Semba, Kazuhiko, Terao, Jun, Tsuji, Yasushi (2012) Copper-Catalyzed Silacarboxylation of Internal Alkynes by Employing Carbon Dioxide and Silylboranes. Angewandte Chemie, 124 (46). 11655-11658 doi:10.1002/ange.201207148
Semba, Kazuhiko, Bessho, Naoto, Fujihara, Tetsuaki, Terao, Jun, Tsuji, Yasushi (2014) Copper-Catalyzed Borylative Allyl-Allyl Coupling Reaction. Angewandte Chemie, 126 (34). 9153-9157 doi:10.1002/ange.201404173
Fujihara, Tetsuaki, Tani, Yosuke, Semba, Kazuhiko, Terao, Jun, Tsuji, Yasushi (2012) Copper-Catalyzed Silacarboxylation of Internal Alkynes by Employing Carbon Dioxide and Silylboranes. Angewandte Chemie International Edition, 51 (46). 11487-11490 doi:10.1002/anie.201207148
Fujihara, Tetsuaki, Yoshikawa, Takahiro, Satou, Motoi, Ohta, Hidetoshi, Terao, Jun, Tsuji, Yasushi (2015) N-Heterocyclic carbene ligands bearing poly(ethylene glycol) chains: effect of the chain length on palladium-catalyzed coupling reactions employing aryl chlorides. Chemical Communications, 51 (98). 17382-17385 doi:10.1039/c5cc07588b
 
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 20, 2025 12:42:09
Go to top of page