Vote for your favorite mineral in #MinCup25! - Calcite vs. Perovskite
This match of heavy hitters is bound to end in heartbreak as classic calcite faces off against futuristic perovskite.
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

Mandal, Tanmay, Zhao, Cong-Gui (2008) Modularly Designed Organocatalytic Assemblies for Direct Nitro-Michael Addition Reactions. Angewandte Chemie, 120 (40). 7828-7831 doi:10.1002/ange.200803236

Advanced
   -   Only viewable:
Reference TypeJournal (article/letter/editorial)
TitleModularly Designed Organocatalytic Assemblies for Direct Nitro-Michael Addition Reactions
JournalAngewandte Chemie
AuthorsMandal, TanmayAuthor
Zhao, Cong-GuiAuthor
Year2008 (September 22)Volume120
Issue40
PublisherWiley
DOIdoi:10.1002/ange.200803236Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID7310023Long-form Identifiermindat:1:5:7310023:8
GUID0
Full ReferenceMandal, Tanmay, Zhao, Cong-Gui (2008) Modularly Designed Organocatalytic Assemblies for Direct Nitro-Michael Addition Reactions. Angewandte Chemie, 120 (40). 7828-7831 doi:10.1002/ange.200803236
Plain TextMandal, Tanmay, Zhao, Cong-Gui (2008) Modularly Designed Organocatalytic Assemblies for Direct Nitro-Michael Addition Reactions. Angewandte Chemie, 120 (40). 7828-7831 doi:10.1002/ange.200803236
In(2008, September) Angewandte Chemie Vol. 120 (40) Wiley

See Also

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

Mandal, Tanmay, Zhao, Cong-Gui (2008) Modularly Designed Organocatalytic Assemblies for Direct Nitro-Michael Addition Reactions. Angewandte Chemie International Edition, 47 (40). 7714-7717 doi:10.1002/anie.200803236
Mandal, Tanmay, Samanta, Sampak, Zhao, Cong-Gui (2007) Organocatalytic Highly Enantioselective Nitroaldol Reaction of α-Ketophosphonates and Nitromethane†. Organic Letters, 9. 943-945 doi:10.1021/ol070209i
Zhao, Gui-Ling, Rios, Ramon, Vesely, Jan, Eriksson, Lars, Córdova, Armando (2008) Organocatalytic Enantioselective Aminosulfenylation of α,β-Unsaturated Aldehydes. Angewandte Chemie, 120 (44). 8596-8600 doi:10.1002/ange.200802335
Tan, Bin, Hernández-Torres, Gloria, Barbas, Carlos F. (2012) Rationally Designed Amide Donors for Organocatalytic Asymmetric Michael Reactions. Angewandte Chemie, 124 (22). 5477-5481 doi:10.1002/ange.201200996
Sinha, Debarshi, Perera, Sandun, Zhao, John Cong-Gui (2013) Highly Enantioselective Inverse-Electron-Demand Hetero-Diels-Alder Reactions Catalyzed by Modularly Designed Organocatalysts. Chemistry - A European Journal, 19 (22). 6976-6979 doi:10.1002/chem.201300168
Alonso, Diego A., Kitagaki, Shinji, Utsumi, Naoto, Barbas, Carlos F. (2008) Towards Organocatalytic Polyketide Synthases with Diverse Electrophile Scope: Trifluoroethyl Thioesters as Nucleophiles in Organocatalytic Michael Reactions and Beyond. Angewandte Chemie, 120 (24). 4664-4667 doi:10.1002/ange.200801088
Lu, Min, Zhu, Di, Lu, Yunpeng, Hou, Yuxuan, Tan, Bin, Zhong, Guofu (2008) Organocatalytic Asymmetric α-Aminoxylation/Aza-Michael Reactions for the Synthesis of Functionalized Tetrahydro-1,2-oxazines. Angewandte Chemie, 120 (52). 10164 doi:10.1002/ange.200890323
Lu, Min, Zhu, Di, Lu, Yunpeng, Hou, Yuxuan, Tan, Bin, Zhong, Guofu (2008) Organocatalytic Asymmetric α-Aminoxylation/Aza-Michael Reactions for the Synthesis of Functionalized Tetrahydro-1,2-oxazines. Angewandte Chemie, 120 (52). 10341-10345 doi:10.1002/ange.200803731
Rana, Nirmal K., Huang, Huicai, Zhao, John C.-G. (2014) Highly Diastereodivergent Synthesis of Tetrasubstituted Cyclohexanes Catalyzed by Modularly Designed Organocatalysts. Angewandte Chemie, 126 (29). 7749-7753 doi:10.1002/ange.201404072
Gupta, Vaishali, Sudhir, Sai, Mandal, Tanmay, Schneider, Christoph (2012) Organocatalytic, Highly Enantioselective Vinylogous Mukaiyama-Michael Reaction of Acyclic Dienol Silyl Ethers. Angewandte Chemie International Edition, 51 (50). 12609-12612 doi:10.1002/anie.201207058
Zhao, Kun, Zhi, Ying, Shu, Tao, Valkonen, Arto, Rissanen, Kari, Enders, Dieter (2016) Organocatalytic Domino Oxa-Michael/1,6-Addition Reactions: Asymmetric Synthesis of Chromans Bearing Oxindole Scaffolds. Angewandte Chemie, 128 (39). 12283-12287 doi:10.1002/ange.201606947
 
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 4, 2025 08:04:52
Go to top of page