Vote for your favorite mineral in #MinCup25! - Zunyite vs. Molybdenite
It's the visually-unmistakable #zunyite vs the physically funky #molybdenite.
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

Mennie, Katrina M., Banik, Steven M., Reichert, Elaine C., Jacobsen, Eric N. (2018) Catalytic Diastereo- and Enantioselective Fluoroamination of Alkenes. Journal Of The American Chemical Society, 140 (14) 4797-4802 doi:10.1021/jacs.8b02143

Advanced
   -   Only viewable:
Reference TypeJournal (article/letter/editorial)
TitleCatalytic Diastereo- and Enantioselective Fluoroamination of Alkenes
JournalJournal Of The American Chemical Society
AuthorsMennie, Katrina M.Author
Banik, Steven M.Author
Reichert, Elaine C.Author
Jacobsen, Eric N.Author
Year2018 (April 11)Volume140
Issue14
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/jacs.8b02143Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID1796762Long-form Identifiermindat:1:5:1796762:8
GUID0
Full ReferenceMennie, Katrina M., Banik, Steven M., Reichert, Elaine C., Jacobsen, Eric N. (2018) Catalytic Diastereo- and Enantioselective Fluoroamination of Alkenes. Journal Of The American Chemical Society, 140 (14) 4797-4802 doi:10.1021/jacs.8b02143
Plain TextMennie, Katrina M., Banik, Steven M., Reichert, Elaine C., Jacobsen, Eric N. (2018) Catalytic Diastereo- and Enantioselective Fluoroamination of Alkenes. Journal Of The American Chemical Society, 140 (14) 4797-4802 doi:10.1021/jacs.8b02143
In(2018, April) Journal Of The American Chemical Society Vol. 140 (14) American Chemical Society (ACS)

See Also

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

Banik, Steven M., Mennie, Katrina M., Jacobsen, Eric N. (2017) Catalytic 1,3-Difunctionalization via Oxidative C–C Bond Activation. Journal Of The American Chemical Society, 139 (27) 9152-9155 doi:10.1021/jacs.7b05160
Woerly, Eric M., Banik, Steven M., Jacobsen, Eric N. (2016) Enantioselective, Catalytic Fluorolactonization Reactions with a Nucleophilic Fluoride Source. Journal Of The American Chemical Society, 138 (42) 13858-13861 doi:10.1021/jacs.6b09499
Banik, Steven M., Medley, Jonathan William, Jacobsen, Eric N. (2016) Catalytic, Diastereoselective 1,2-Difluorination of Alkenes. Journal Of The American Chemical Society, 138 (15) 5000-5003 doi:10.1021/jacs.6b02391
Sharma, Hayden A., Mennie, Katrina M., Kwan, Eugene E., Jacobsen, Eric N. (2020) Enantioselective Aryl-Iodide-Catalyzed Wagner–Meerwein Rearrangements. Journal of the American Chemical Society, 142 (37) 16090-16096 doi:10.1021/jacs.0c08150
Haj, Moriana K., Banik, Steven M., Jacobsen, Eric N. (2019) Catalytic, Enantioselective 1,2-Difluorination of Cinnamamides. Organic Letters, 21. 4919-4923 doi:10.1021/acs.orglett.9b00938
Banik, Steven M., Medley, Jonathan William, Jacobsen, Eric N. (2016) Catalytic, asymmetric difluorination of alkenes to generate difluoromethylated stereocenters. Science, 353 (6294). 51-54 doi:10.1126/science.aaf8078
Ronchi, Elisabetta, Paradine, Shauna M., Jacobsen, Eric N. (2021) Enantioselective, Catalytic Multicomponent Synthesis of Homoallylic Amines Enabled by Hydrogen-Bonding and Dispersive Interactions. Journal of the American Chemical Society, 143 (19) 7272-7278 doi:10.1021/jacs.1c03024
Hao, Wei, Harenberg, Johannes H., Wu, Xiangyu, MacMillan, Samantha N., Lin, Song (2018) Diastereo- and Enantioselective Formal [3 + 2] Cycloaddition of Cyclopropyl Ketones and Alkenes via Ti-Catalyzed Radical Redox Relay. Journal Of The American Chemical Society, 140 (10) 3514-3517 doi:10.1021/jacs.7b13710
Levin, Mark D., Ovian, John M., Read, Jacquelyne A., Sigman, Matthew S., Jacobsen, Eric N. (2020) Catalytic Enantioselective Synthesis of Difluorinated Alkyl Bromides. Journal of the American Chemical Society, 142 (35) 14831-14837 doi:10.1021/jacs.0c07043
You, Wei, Brown, M. Kevin (2015) Catalytic Enantioselective Diarylation of Alkenes. Journal Of The American Chemical Society, 137 (46) 14578-14581 doi:10.1021/jacs.5b10176
Mumford, Emily M., Hemric, Brett N., Denmark, Scott E. (2021) Catalytic, Enantioselective Syn-Oxyamination of Alkenes. Journal of the American Chemical Society, 143 (33) 13408-13417 doi:10.1021/jacs.1c06750
 
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 12, 2025 10:48:54
Go to top of page