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Kumagai, Naoya, Shibasaki, Masakatsu (2016) Nucleophilic and Electrophilic Activation of Non-Heteroaromatic Amides in Atom-Economical Asymmetric Catalysis. Chemistry - A European Journal, 22 (43). 15192-15200 doi:10.1002/chem.201602484

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Reference TypeJournal (article/letter/editorial)
TitleNucleophilic and Electrophilic Activation of Non-Heteroaromatic Amides in Atom-Economical Asymmetric Catalysis
JournalChemistry - A European Journal
AuthorsKumagai, NaoyaAuthor
Shibasaki, MasakatsuAuthor
Year2016 (October 17)Volume22
Issue43
PublisherWiley
DOIdoi:10.1002/chem.201602484Search in ResearchGate
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Mindat Ref. ID8266258Long-form Identifiermindat:1:5:8266258:1
GUID0
Full ReferenceKumagai, Naoya, Shibasaki, Masakatsu (2016) Nucleophilic and Electrophilic Activation of Non-Heteroaromatic Amides in Atom-Economical Asymmetric Catalysis. Chemistry - A European Journal, 22 (43). 15192-15200 doi:10.1002/chem.201602484
Plain TextKumagai, Naoya, Shibasaki, Masakatsu (2016) Nucleophilic and Electrophilic Activation of Non-Heteroaromatic Amides in Atom-Economical Asymmetric Catalysis. Chemistry - A European Journal, 22 (43). 15192-15200 doi:10.1002/chem.201602484
In(2016, October) Chemistry - A European Journal Vol. 22 (43) Wiley

See Also

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Zhang, Ming, Kumagai, Naoya, Shibasaki, Masakatsu (2016) Electrophilic Activation of α,β-Unsaturated Amides: Catalytic Asymmetric Vinylogous Conjugate Addition of Unsaturated γ-Butyrolactones. Chemistry - A European Journal, 22 (16). 5525-5529 doi:10.1002/chem.201600740
Lin, Shaoquan, Kumagai, Naoya, Shibasaki, Masakatsu (2016) Direct Catalytic Asymmetric Mannich-type Reaction of α,β-Unsaturated γ-Butyrolactam with Ketimines. Chemistry - A European Journal, 22 (10). 3296-3299 doi:10.1002/chem.201600034
Zhang, Ming, Kumagai, Naoya, Shibasaki, Masakatsu (2017) α,β-Unsaturated Amides as Dipolarophiles: Catalytic Asymmetric exo -Selective 1,3-Dipolar Cycloaddition with Nitrones. Chemistry - A European Journal, 23 (51). 12424 doi:10.1002/chem.201703250
Hashimoto, Kazuki, Kumagai, Naoya, Shibasaki, Masakatsu (2015) A Carbon Nanotube Confinement Strategy to Implement Homogeneous Asymmetric Catalysis in the Solid Phase. Chemistry - A European Journal, 21 (11). 4262-4266 doi:10.1002/chem.201406402
Kawato, Yuji, Chaudhary, Sandeep, Kumagai, Naoya, Shibasaki, Masakatsu (2013) Streamlined Catalytic Asymmetric Synthesis of Atorvastatin. Chemistry - A European Journal, 19 (12). 3802-3806 doi:10.1002/chem.201204609
Berhal, Farouk, Takechi, Sho, Kumagai, Naoya, Shibasaki, Masakatsu (2011) Catalytic Asymmetric Amination of N-Nonsubstituted α-Alkoxycarbonyl Amides: Concise Enantioselective Synthesis of Mycestericin F and G. Chemistry - A European Journal, 17 (6). 1915-1921 doi:10.1002/chem.201002874
Zhang, Ming, Kumagai, Naoya, Shibasaki, Masakatsu (2017) Front Picture: α,β-Unsaturated Amides as Dipolarophiles: Catalytic Asymmetric exo -Selective 1,3-Dipolar Cycloaddition with Nitrones (Chem. Eur. J. 51/2017). Chemistry - A European Journal, 23 (51). 12420 doi:10.1002/chem.201703251
Suzuki, Yuta, Yazaki, Ryo, Kumagai, Naoya, Shibasaki, Masakatsu (2011) Direct Catalytic Asymmetric Intramolecular Conjugate Addition of Thioamide to α,β-Unsaturated Esters. Chemistry - A European Journal, 17 (43). 11998-12001 doi:10.1002/chem.201102332
Sun, Zhongdong, Weidner, Karin, Kumagai, Naoya, Shibasaki, Masakatsu (2015) Direct Catalytic Asymmetric Mannich-Type Reaction of α-N3Amide. Chemistry - A European Journal, 21 (49). 17574-17577 doi:10.1002/chem.201503921
Yoshida, Takamasa, Morimoto, Hiroyuki, Kumagai, Naoya, Matsunaga, Shigeki, Shibasaki, Masakatsu (2005) Non-C2-Symmetric, Chirally Economical, and Readily Tunable Linked-binols: Design and Application in a Direct Catalytic Asymmetric Mannich-Type Reaction. Angewandte Chemie, 117 (22). 3536-3540 doi:10.1002/ange.200500425
Yoshida, Takamasa, Morimoto, Hiroyuki, Kumagai, Naoya, Matsunaga, Shigeki, Shibasaki, Masakatsu (2005) Non-C2-Symmetric, Chirally Economical, and Readily Tunable Linked-binols: Design and Application in a Direct Catalytic Asymmetric Mannich-Type Reaction. Angewandte Chemie International Edition, 44 (22). 3470-3474 doi:10.1002/anie.200500425
 
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