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 NO 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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