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Nakatsuji, Yuya, Kobayashi, Yusuke, Takemoto, Yoshiji (2019) Direct Addition of Amides to Glycals Enabled by Solvation‐Insusceptible 2‐Haloazolium Salt Catalysis. Angewandte Chemie International Edition, 58 (40). 14115-14119 doi:10.1002/anie.201907129

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Reference TypeJournal (article/letter/editorial)
TitleDirect Addition of Amides to Glycals Enabled by Solvation‐Insusceptible 2‐Haloazolium Salt Catalysis
JournalAngewandte Chemie International Edition
AuthorsNakatsuji, YuyaAuthor
Kobayashi, YusukeAuthor
Takemoto, YoshijiAuthor
Year2019 (October)Volume58
Issue40
PublisherWiley
DOIdoi:10.1002/anie.201907129Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID8652334Long-form Identifiermindat:1:5:8652334:1
GUID0
Full ReferenceNakatsuji, Yuya, Kobayashi, Yusuke, Takemoto, Yoshiji (2019) Direct Addition of Amides to Glycals Enabled by Solvation‐Insusceptible 2‐Haloazolium Salt Catalysis. Angewandte Chemie International Edition, 58 (40). 14115-14119 doi:10.1002/anie.201907129
Plain TextNakatsuji, Yuya, Kobayashi, Yusuke, Takemoto, Yoshiji (2019) Direct Addition of Amides to Glycals Enabled by Solvation‐Insusceptible 2‐Haloazolium Salt Catalysis. Angewandte Chemie International Edition, 58 (40). 14115-14119 doi:10.1002/anie.201907129
In(2019, October) Angewandte Chemie International Edition Vol. 58 (40) Wiley

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Nakatsuji, Yuya, Kobayashi, Yusuke, Takemoto, Yoshiji (2019) Direct Addition of Amides to Glycals Enabled by Solvation‐Insusceptible 2‐Haloazolium Salt Catalysis. Angewandte Chemie, 131 (40). 14253-14257 doi:10.1002/ange.201907129
Kobayashi, Yusuke, Nakatsuji, Yuya, Li, Shanji, Tsuzuki, Seiji, Takemoto, Yoshiji (2018) Direct N -Glycofunctionalization of Amides with Glycosyl Trichloroacetimidate by Thiourea/Halogen Bond Donor Co-Catalysis. Angewandte Chemie International Edition, 57 (14). 3646-3650 doi:10.1002/anie.201712726
Kobayashi, Yusuke, Nakatsuji, Yuya, Li, Shanji, Tsuzuki, Seiji, Takemoto, Yoshiji (2018) Direct N -Glycofunctionalization of Amides with Glycosyl Trichloroacetimidate by Thiourea/Halogen Bond Donor Co-Catalysis. Angewandte Chemie, 130 (14). 3708-3712 doi:10.1002/ange.201712726
Izumi, Sanae, Kobayashi, Yusuke, Takemoto, Yoshiji (2020) Stereoselective Synthesis of 1,1′‐Disaccharides by Organoboron Catalysis. Angewandte Chemie International Edition, 59 (33) 14054-14059 doi:10.1002/anie.202004476
Saito, Masato, Kobayashi, Yusuke, Tsuzuki, Seiji, Takemoto, Yoshiji (2017) Electrophilic Activation of Iodonium Ylides by Halogen-Bond-Donor Catalysis for Cross-Enolate Coupling. Angewandte Chemie International Edition, 56 (26). 7653-7657 doi:10.1002/anie.201703641
Kobayashi, Yusuke, Masakado, Sota, Takemoto, Yoshiji (2018) Photoactivated N ‐Acyliminoiodinanes Applied to Amination: an ortho ‐Methoxymethyl Group Stabilizes Reactive Precursors. Angewandte Chemie International Edition, 57 (3). 693-697 doi:10.1002/anie.201710277
Kobayashi, Yusuke, Taniguchi, Yamato, Hayama, Noboru, Inokuma, Tsubasa, Takemoto, Yoshiji (2013) A Powerful Hydrogen-Bond-Donating Organocatalyst for the Enantioselective Intramolecular Oxa-Michael Reaction of α,β-Unsaturated Amides and Esters. Angewandte Chemie International Edition, 52 (42). 11114-11118 doi:10.1002/anie.201305492
Izumi, Sanae, Kobayashi, Yusuke, Takemoto, Yoshiji (2020) Stereoselective Synthesis of 1,1′‐Disaccharides by Organoboron Catalysis. Angewandte Chemie, 132 (33) 14158-14163 doi:10.1002/ange.202004476
Hoashi, Yasutaka, Okino, Tomotaka, Takemoto, Yoshiji (2005) Enantioselective Michael Addition to α,β-Unsaturated Imides Catalyzed by a Bifunctional Organocatalyst. Angewandte Chemie International Edition, 44 (26). 4032-4035 doi:10.1002/anie.200500459
Miyabe, Hideto, Asada, Ryuta, Toyoda, Akira, Takemoto, Yoshiji (2006) Enantioselective Cascade Radical Addition–Cyclization–Trapping Reactions. Angewandte Chemie International Edition, 45 (35). 5863-5866 doi:10.1002/anie.200602042
Saito, Masato, Kobayashi, Yusuke, Tsuzuki, Seiji, Takemoto, Yoshiji (2017) Electrophilic Activation of Iodonium Ylides by Halogen-Bond-Donor Catalysis for Cross-Enolate Coupling. Angewandte Chemie, 129 (26). 7761-7765 doi:10.1002/ange.201703641
 
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