Year |
Citation |
Score |
2023 |
Toda Y, Iwasaki M, Suga H. Base-mediated synthesis of cyclic dithiocarbamates from 1-amino-3-chloropropan-2-ol derivatives and carbon disulfide. Organic & Biomolecular Chemistry. PMID 37486165 DOI: 10.1039/d3ob01070h |
0.331 |
|
2022 |
Toda Y, Shiokawa R, Iwasaki M, Yamaguchi D, Kawamura K, Sukegawa K, Suga H. Tetraarylphosphonium salt-catalyzed formal [3+2] cycloaddition between epoxides and trichloroacetonitrile for the synthesis of β-amino alcohol derivatives. Chemical Communications (Cambridge, England). PMID 36189849 DOI: 10.1039/d2cc03782c |
0.301 |
|
2022 |
Toda Y, Sato K, Sato K, Nagasaki K, Nakajima H, Kikuchi A, Sukegawa K, Suga H. Asymmetric Cycloadditions of Acyclic Carbonyl Ylides with Aldehydes Catalyzed by a Chiral Binaphthyldiimine-Ni(II) Complex: Enantioselective Synthesis of 1,3-Dioxolanes and Mechanistic Studies by DFT Calculations. Organic Letters. 24: 4739-4744. PMID 35724970 DOI: 10.1021/acs.orglett.2c01682 |
0.403 |
|
2021 |
Toda Y, Korenaga T, Obayashi R, Kikuchi J, Terada M. Dynamic parallel kinetic resolution of α-ferrocenyl cation initiated by chiral Brønsted acid catalyst. Chemical Science. 12: 10306-10312. PMID 34447532 DOI: 10.1039/d1sc02122b |
0.64 |
|
2021 |
Toda Y, Yoshida T, Arisue K, Fukushima K, Esaki H, Kikuchi A, Suga H. Enantioselective Protonation of Cyclic Carbonyl Ylides by Chiral Lewis Acid Assisted Alcohols. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34002420 DOI: 10.1002/chem.202101491 |
0.389 |
|
2020 |
Toda Y, Hashimoto K, Mori Y, Suga H. A Phosphonium Ylide as a Ligand for [3 + 2] Coupling Reactions of Epoxides with Heterocumulenes under Mild Conditions. The Journal of Organic Chemistry. 85: 10980-10987. PMID 32806088 DOI: 10.1021/Acs.Joc.0C01101 |
0.429 |
|
2020 |
Itoh K, Takashino A, Ohtsuka A, Kobe M, Sawamura S, Kato R, Hirayama S, Karaki F, Mizuguchi T, Sato N, Tokunaga K, Toda Y, Suga H, Ishida H, Fujii H. Synthesis of 1,2,5‐Oxadiazinane Derivatives by Photochemical Cycloaddition of Nitrones with Diaminomethanes Chemphotochem. 4: 388-392. DOI: 10.1002/cptc.202000004 |
0.308 |
|
2019 |
Toda Y, Komiyama Y, Esaki H, Fukushima K, Suga H. Methoxy Groups Increase Reactivity of Bifunctional Tetraarylphosphonium Salt Catalysts for Carbon Dioxide Fixation: A Mechanistic Study. The Journal of Organic Chemistry. PMID 31665605 DOI: 10.1021/Acs.Joc.9B02581 |
0.382 |
|
2019 |
Toda Y, Tanaka S, Gomyou S, Kikuchi A, Suga H. 4-Hydroxymethyl-substituted oxazolidinone synthesis by tetraarylphosphonium salt-catalyzed reactions of glycidols with isocyanates. Chemical Communications (Cambridge, England). PMID 31020962 DOI: 10.1039/C9Cc01983A |
0.503 |
|
2019 |
Toda Y, Matsuda R, Gomyou S, Suga H. Use of trichloroacetonitrile as a hydrogen chloride generator for ring-opening reactions of aziridines. Organic & Biomolecular Chemistry. PMID 30920569 DOI: 10.1039/C9Ob00602H |
0.395 |
|
2019 |
Toda Y, Tanaka K, Matsuda R, Suga H. Visible-light-triggered Catalytic Halohydrin Synthesis from Epoxides and Trichloroacetonitrile by Copper and Iron Salts Chemistry Letters. 48: 1469-1471. DOI: 10.1246/Cl.190679 |
0.34 |
|
2018 |
Suga H, Yoshiwara M, Yamaguchi T, Bando T, Taguchi M, Inaba A, Goto Y, Kikuchi A, Itoh K, Toda Y. Enantioselective synthesis of 8-azabicyclo[3.2.1]octanes via asymmetric 1,3-dipolar cycloadditions of cyclic azomethine ylides using a dual catalytic system. Chemical Communications (Cambridge, England). PMID 30560972 DOI: 10.1039/C8Cc09224A |
0.534 |
|
2018 |
Toda Y, Kaku W, Tsuruoka M, Shinogaki S, Abe T, Kamiya H, Kikuchi A, Itoh K, Suga H. Three-Component Reactions of Diazoesters, Aldehydes, and Imines Using a Dual Catalytic System Consisting of a Rhodium(II) Complex and a Lewis Acid. Organic Letters. PMID 29671597 DOI: 10.1021/Acs.Orglett.8B00865 |
0.449 |
|
2018 |
Suga H, Iwai T, Shimizu M, Takahashi K, Toda Y. Efficient generation of an oxidopyrylium ylide using a Pd catalyst and its [5+2] cycloadditions with several dipolarophiles. Chemical Communications (Cambridge, England). PMID 29333548 DOI: 10.1039/C7Cc09552J |
0.425 |
|
2018 |
Suga H, Toda Y, Koyama M, Fukushima K, Esaki H. Enantioselective Cycloadditions between Aliphatic Nitrile Oxides and 2-Hydroxystyrenes Catalyzed by Chiral Amine-Urea Heterocycles. 97: 147. DOI: 10.3987/Com-17-S(T)7 |
0.466 |
|
2018 |
Toda Y, Shimizu M, Iwai T, Suga H. Triethylamine Enables Catalytic Generation of Oxidopyrylium Ylides for [5+2] Cycloadditions with Alkenes: An Efficient Entry to 8-Oxabicyclo[3.2.1]octane Frameworks Advanced Synthesis & Catalysis. 360: 2377-2381. DOI: 10.1002/Adsc.201800290 |
0.419 |
|
2017 |
Toda Y, Gomyou S, Tanaka S, Komiyama Y, Kikuchi A, Suga H. Tetraarylphosphonium Salt-Catalyzed Synthesis of Oxazolidinones from Isocyanates and Epoxides. Organic Letters. PMID 29039956 DOI: 10.1021/Acs.Orglett.7B02722 |
0.526 |
|
2017 |
Suga H, Hashimoto Y, Toda Y, Fukushima K, Esaki H, Kikuchi A. Amine-urea Mediated Asymmetric Cycloadditions between Nitrile Oxides and o-Hydroxystyrenes by Dual Activation, and Their Computational Studies. Angewandte Chemie (International Ed. in English). PMID 28752651 DOI: 10.1002/Anie.201705662 |
0.394 |
|
2017 |
Toda Y, Sakamoto T, Komiyama Y, Kikuchi A, Suga H. A Phosphonium Ylide as an Ionic Nucleophilic Catalyst for Primary Hydroxyl Group Selective Acylation of Diols Acs Catalysis. 7: 6150-6154. DOI: 10.1021/Acscatal.7B02281 |
0.452 |
|
2016 |
Terada M, Ota Y, Li F, Toda Y, Kondoh A. Enantio-Convergent Nucleophilic Substitution Reaction of Racemic Alkyne-Dicobalt Complex (Nicholas Reaction) Catalyzed by Chiral Brønsted Acid. Journal of the American Chemical Society. PMID 27490239 DOI: 10.1021/Jacs.6B05948 |
0.676 |
|
2016 |
Toda Y, Komiyama Y, Kikuchi A, Suga H. Tetraarylphosphonium Salt-Catalyzed Carbon Dioxide Fixation at Atmospheric Pressure for the Synthesis of Cyclic Carbonates Acs Catalysis. 6: 6906-6910. DOI: 10.1021/Acscatal.6B02265 |
0.393 |
|
2015 |
Suga H, Sekikawa Y, Misawa S, Kinugawa D, Oda R, Itoh K, Toda Y, Kiyono R. Chiral Lewis Acid-Catalyzed Enantioselective Cycloadditions between Indoles and Cyclic Carbonyl Ylides Derived from Diazodiketone or Diazoketoester Derivatives. The Journal of Organic Chemistry. PMID 26106799 DOI: 10.1021/Acs.Joc.5B00835 |
0.578 |
|
2014 |
Toda Y, Pink M, Johnston JN. Brønsted acid catalyzed phosphoramidic acid additions to alkenes: diastereo- and enantioselective halogenative cyclizations for the synthesis of C- and P-chiral phosphoramidates. Journal of the American Chemical Society. 136: 14734-7. PMID 25336273 DOI: 10.1021/Ja5088584 |
0.646 |
|
2014 |
Terada M, Komuro T, Toda Y, Korenaga T. Mechanistic studies of highly enantio- and diastereoselective aza-Petasis-Ferrier rearrangement catalyzed by chiral phosphoric acid. Journal of the American Chemical Society. 136: 7044-57. PMID 24746095 DOI: 10.1021/Ja5017206 |
0.63 |
|
2014 |
Terada M, Li F, Toda Y. Chiral silver phosphate catalyzed transformation of ortho-alkynylaryl ketones into 1H-isochromene derivatives through an intramolecular-cyclization/enantioselective-reduction sequence. Angewandte Chemie (International Ed. in English). 53: 235-9. PMID 24273203 DOI: 10.1002/Anie.201307371 |
0.658 |
|
2014 |
Kanomata K, Toda Y, Shibata Y, Yamanaka M, Tsuzuki S, Gridnev ID, Terada M. Secondary stereocontrolling interactions in chiral Brønsted acid catalysis: Study of a Petasis-Ferrier-type rearrangement catalyzed by chiral phosphoric acids Chemical Science. 5: 3515-3523. DOI: 10.1039/C4Sc00611A |
0.529 |
|
2013 |
Terada M, Yamanaka T, Toda Y. Chiral anion catalysis in the enantioselective 1,4-reduction of the 1-benzopyrylium ion as a reactive intermediate. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 13658-62. PMID 24092538 DOI: 10.1002/Chem.201302486 |
0.622 |
|
2013 |
Toda Y, Terada M. Relay catalysis by a ruthenium complex-chiral bronsted acid binary sytem for ternary reaction sequence involving enantioselective pictet-spengler-type cyclization as the key step Synlett. 24: 752-756. DOI: 10.1055/S-0032-1318302 |
0.551 |
|
2012 |
Terada M, Toda Y. Relay catalysis using a rhodium complex/chiral Brønsted acid binary system: enantioselective reduction of a carbonyl ylide as the reactive intermediate. Angewandte Chemie (International Ed. in English). 51: 2093-7. PMID 22262558 DOI: 10.1002/Anie.201107805 |
0.657 |
|
2009 |
Terada M, Toda Y. Double bond isomerization/enantioselective aza-Petasis-Ferrier rearrangement sequence as an efficient entry to anti- and enantioenriched beta-amino aldehydes. Journal of the American Chemical Society. 131: 6354-5. PMID 19374414 DOI: 10.1021/Ja902202G |
0.65 |
|
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