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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

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Reference TypeJournal (article/letter/editorial)
Titleα,β-Unsaturated Amides as Dipolarophiles: Catalytic Asymmetric exo -Selective 1,3-Dipolar Cycloaddition with Nitrones
JournalChemistry - A European Journal
AuthorsZhang, MingAuthor
Kumagai, NaoyaAuthor
Shibasaki, MasakatsuAuthor
Year2017 (September 12)Volume23
Issue51
PublisherWiley
DOIdoi:10.1002/chem.201703250Search in ResearchGate
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Mindat Ref. ID8271498Long-form Identifiermindat:1:5:8271498:1
GUID0
Full ReferenceZhang, 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
Plain TextZhang, 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
In(2017, September) Chemistry - A European Journal Vol. 23 (51) Wiley

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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
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
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
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
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
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
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
Ogawa, Takanori, Kumagai, Naoya, Shibasaki, Masakatsu (2012) Catalytic Asymmetric Conjugate Addition of Thiols to α,β-Unsaturated Thioamides: Expeditious Access to Enantioenriched 1,5-Benzothiazepines. Angewandte Chemie International Edition, 51 (34). 8551-8554 doi:10.1002/anie.201204365
Ogawa, Takanori, Mouri, Shinsuke, Yazaki, Ryo, Kumagai, Naoya, Shibasaki, Masakatsu (2012) Intermediate as Catalyst: Catalytic Asymmetric Conjugate Addition of Nitroalkanes to α,β-Unsaturated Thioamides. Organic Letters, 14. 110-113 doi:10.1021/ol202898e
Yin, Liang, Takada, Hisashi, Lin, Shaoquan, Kumagai, Naoya, Shibasaki, Masakatsu (2014) Direct Catalytic Asymmetric Vinylogous Conjugate Addition of Unsaturated Butyrolactones to α,β-Unsaturated Thioamides. Angewandte Chemie, 126 (21). 5431-5435 doi:10.1002/ange.201402332
 
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