Norie Momiyama, Ph.D. - Publications

Affiliations: 
2005 University of Chicago, Chicago, IL 
Area:
organoaluminum chemistry

33 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Oishi S, Fujinami T, Masui Y, Suzuki T, Kato M, Ohtsuka N, Momiyama N. Protocol for efficient dearomatization of N-heteroaromatics with halogen(I) complex catalyst. Star Protocols. 4: 102140. PMID 36892997 DOI: 10.1016/j.xpro.2023.102140  0.398
2022 Momiyama N, Jongwohan C, Ohtsuka N, Chaibuth P, Fujinami T, Adachi K, Suzuki T. Chiral Counteranion-Directed Catalytic Asymmetric Methylene Migration Reaction of Ene-Aldimines. The Journal of Organic Chemistry. PMID 35736506 DOI: 10.1021/acs.joc.2c00742  0.448
2022 Tanaka K, Kishimoto M, Tanaka Y, Kamiyama Y, Asada Y, Sukekawa M, Ohtsuka N, Suzuki T, Momiyama N, Honda K, Hoshino Y. Moderately Oxidizing Thioxanthylium Organophotoredox Catalysts for Radical-Cation Diels-Alder Reactions. The Journal of Organic Chemistry. PMID 35142514 DOI: 10.1021/acs.joc.1c02972  0.347
2021 Momiyama N, Izumiseki A, Ohtsuka N, Suzuki T. Correlations between Substituent Effects and Catalytic Activities: A Quantitative Approach for the Development of Halogen-Bonding-Driven Anion-Binding Catalysts. Chempluschem. 86: 913-919. PMID 34145787 DOI: 10.1002/cplu.202100147  0.35
2021 Momiyama N, Izumiseki A, Ohtsuka N, Suzuki T. Correlations between Substituent Effects and Catalytic Activities: A Quantitative Approach for the Development of Halogen-Bonding-Driven Anion-Binding Catalysts. Chempluschem. 86: 913-919. PMID 34145787 DOI: 10.1002/cplu.202100147  0.35
2019 Jongwohan C, Honda Y, Suzuki T, Fujinami T, Adachi K, Momiyama N. Brønsted Acid-Initiated Formal [1,3]-Rearrangement Dictated by β-Substituted Ene-Aldimines. Organic Letters. PMID 31247769 DOI: 10.1021/Acs.Orglett.9B01533  0.494
2016 Momiyama N, Tabuse H, Noda H, Yamanaka M, Fujinami T, Yamanishi K, Izumiseki A, Funayama K, Egawa F, Okada S, Adachi H, Terada M. Molecular Design of a Chiral Brønsted Acid with Two Different Acidic Sites: Regio-, Diastereo-, and Enantioselective Hetero-Diels-Alder Reaction of Azopyridinecarboxylate with Amidodienes Catalyzed by Chiral Carboxylic Acid-Monophosphoric Acid. Journal of the American Chemical Society. PMID 27529134 DOI: 10.1021/Jacs.6B07150  0.553
2016 Kikuchi J, Momiyama N, Terada M. Chiral Phosphoric Acid Catalyzed Diastereo- and Enantioselective Mannich-Type Reaction between Enamides and Thiazolones. Organic Letters. PMID 27175571 DOI: 10.1021/Acs.Orglett.6B00857  0.558
2016 Momiyama N, Okamoto H, Kikuchi J, Korenaga T, Terada M. Perfluorinated Aryls in the Design of Chiral Brønsted Acid Catalysts: Catalysis of Enantioselective [4 + 2] Cycloadditions and Ene Reactions of Imines with Alkenes by Chiral Mono-Phosphoric Acids with Perfluoroaryls Acs Catalysis. 6: 1198-1204. DOI: 10.1021/Acscatal.5B02136  0.612
2016 Momiyama N, Funayama K, Noda H, Yamanaka M, Akasaka N, Ishida S, Iwamoto T, Terada M. Hydrogen Bonds-Enabled Design of a C1-Symmetric Chiral Brønsted Acid Catalyst Acs Catalysis. 6: 949-956. DOI: 10.1021/Acscatal.5B02079  0.568
2015 Momiyama N, Narumi T, Terada M. Design of a Brønsted acid with two different acidic sites: synthesis and application of aryl phosphinic acid-phosphoric acid as a Brønsted acid catalyst. Chemical Communications (Cambridge, England). PMID 26445921 DOI: 10.1039/C5Cc06787A  0.534
2015 Momiyama N, Okamoto H, Shimizu M, Terada M. Synthetic Method for 2,2'-Disubstituted Fluorinated Binaphthyl Derivatives and Application as Chiral Source in Design of Chiral Mono-Phosphoric Acid Catalyst. Chirality. PMID 25665035 DOI: 10.1002/Chir.22429  0.577
2012 Momiyama N, Terada M, Konno T, Furiya Y, Iwamoto T. Bis-Phosphoric Acid: Two is Better than One Synfacts. 8: 0348-0348. DOI: 10.1055/s-0031-1290491  0.31
2011 Momiyama N, Konno T, Furiya Y, Iwamoto T, Terada M. Design of chiral bis-phosphoric acid catalyst derived from (R)-3,3'-di(2-hydroxy-3-arylphenyl)binaphthol: catalytic enantioselective Diels-Alder reaction of α,β-unsaturated aldehydes with amidodienes. Journal of the American Chemical Society. 133: 19294-7. PMID 22066907 DOI: 10.1021/Ja2081444  0.591
2011 Momiyama N, Nishimoto H, Terada M. Chiral Brønsted acid catalysis for enantioselective Hosomi-Sakurai reaction of imines with allyltrimethylsilane. Organic Letters. 13: 2126-9. PMID 21434633 DOI: 10.1021/Ol200595B  0.528
2010 Momiyama N, Yamamoto H. ChemInform Abstract: Lewis Acid Promoted, O-Selective, Nucleophilic Addition of Silyl Enol Ethers to N=O Bonds. Cheminform. 33: no-no. DOI: 10.1002/chin.200250033  0.352
2010 Terada M, Momiyama N. Enantioselective Synthesis of Amines by Chiral Brønsted Acid Catalysts Chiral Amine Synthesis: Methods, Developments and Applications. 75-129. DOI: 10.1002/9783527629541.ch3  0.535
2009 Momiyama N, Tabuse H, Terada M. Chiral phosphoric acid-governed anti-diastereoselective and enantioselective hetero-Diels-Alder reaction of glyoxylate. Journal of the American Chemical Society. 131: 12882-3. PMID 19694430 DOI: 10.1021/Ja904749X  0.595
2008 Terada M, Soga K, Momiyama N. Enantioselective activation of aldehydes by chiral phosphoric acid catalysts in an aza-ene-type reaction between glyoxylate and enecarbamate. Angewandte Chemie (International Ed. in English). 47: 4122-5. PMID 18421736 DOI: 10.1002/Anie.200800232  0.603
2008 Terada M, Soga K, Momiyama N. Aldehyde Activation by Binol-Derived Phosphoric Acids Synfacts. 2008: 0765-0765. DOI: 10.1055/s-2008-1077821  0.327
2008 Saito S, Momiyama N, Yamamoto H. Development of organocatalysis based on the molecular design of pyrrolidine-Brønsted acid catalysts Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry. 66: 774-784.  0.575
2007 Momiyama N, Yamamoto Y, Yamamoto H. Diastereo- and enantioselective synthesis of nitroso Diels-Alder-type bicycloketones using dienamine: mechanistic insight into sequential nitroso Aldol/Michael reaction and application for optically pure 1-amino-3,4-diol synthesis. Journal of the American Chemical Society. 129: 1190-5. PMID 17263400 DOI: 10.1021/Ja066037M  0.585
2006 Morales MR, Momiyama N, Yamamoto H. Metal-induced reactions of O-nitroso aldol products Synlett. 705-708. DOI: 10.1055/S-2006-933123  0.531
2005 Yamamoto H, Momiyama N. Rich chemistry of nitroso compounds. Chemical Communications (Cambridge, England). 3514-25. PMID 16010311 DOI: 10.1039/B503212C  0.613
2005 Momiyama N, Yamamoto H. Bronsted acid catalysis of achiral enamine for regio- and enantioselective nitroso aldol synthesis. Journal of the American Chemical Society. 127: 1080-1. PMID 15669829 DOI: 10.1021/Ja0444637  0.65
2004 Yamamoto Y, Momiyama N, Yamamoto H. Enantioselective tandem O-nitroso Aldol/Michael reaction. Journal of the American Chemical Society. 126: 5962-3. PMID 15137750 DOI: 10.1021/Ja049741G  0.582
2004 Momiyama N, Yamamoto H. Enantioselective O- and N-nitroso aldol synthesis of tin enolates. Isolation of three BINAP-silver complexes and their role in regio- and enantioselectivity. Journal of the American Chemical Society. 126: 5360-1. PMID 15113198 DOI: 10.1021/Ja039103I  0.586
2004 Momiyama N, Torii H, Saito S, Yamamoto H. O-nitroso aldol synthesis: Catalytic enantioselective route to alpha-aminooxy carbonyl compounds via enamine intermediate. Proceedings of the National Academy of Sciences of the United States of America. 101: 5374-8. PMID 15067138 DOI: 10.1073/Pnas.0307785101  0.656
2003 Momiyama N, Yamamoto H. Catalytic enantioselective synthesis of alpha-aminooxy and alpha-hydroxy ketone using nitrosobenzene. Journal of the American Chemical Society. 125: 6038-9. PMID 12785817 DOI: 10.1021/Ja0298702  0.562
2002 Momiyama N, Yamamoto H. Simple synthesis of alpha-hydroxyamino carbonyl compounds: new scope of the nitroso aldol reaction. Organic Letters. 4: 3579-82. PMID 12375892 DOI: 10.1021/Ol026443K  0.486
2002 Momiyama N, Yamamoto H. Lewis acid promoted, O-selective, nucleophilic addition of silyl enol ethers to NdoublebondO bonds. Angewandte Chemie (International Ed. in English). 41: 2986-8. PMID 12203433 DOI: 10.1002/1521-3773(20020816)41:16<2986::Aid-Anie2986>3.0.Co;2-F  0.525
2002 Momiyama N, Yamamoto H. Lewis Acid Promoted, O-Selective, Nucleophilic Addition of Silyl Enol Ethers to NO bonds Angewandte Chemie International Edition. 41: 3313-3313. DOI: 10.1002/1521-3773(20020916)41:18<3313::Aid-Anie11113313>3.0.Co;2-X  0.525
2002 Momiyama N, Yamamoto H. Lewis Acid Promoted, O-Selective, Nucleophilic Addition of Silyl Enol Ethers to NdO bonds We thank Prof. Akira Yanagisawa (Department of Chemistry, Faculty of Science, Chiba University) for helpful discussion, Dr. Yujiro Hoshino for stimulating discussion and X-ray crystallographic analysis, and Mr. Kin-ichi Oyama (Chemical Instrument Center of Nagoya University) for measurement of ESI mass spectra. Angewandte Chemie. 114: 2986. DOI: 10.1002/1521-3757(20020816)114:16<3112::Aid-Ange3112>3.0.Co;2-N  0.45
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