Year |
Citation |
Score |
2023 |
Hikima R, Takeshima A, Kano T. One-pot furan synthesis through diethylzinc-mediated coupling reaction between two α-bromocarbonyl compounds. Organic & Biomolecular Chemistry. 21: 8463-8466. PMID 37830372 DOI: 10.1039/d3ob01521a |
0.387 |
|
2023 |
Uwaso Y, Yokoyama N, Kano T. Synthesis of biphenyl-based chiral amine catalysts from dibromopyrenes and their application in enamine catalysis. Organic & Biomolecular Chemistry. 21: 6484-6487. PMID 37526571 DOI: 10.1039/d3ob01059g |
0.472 |
|
2023 |
Hikawa R, Shimogaki M, Kano T. Construction of three contiguous stereocenters through amine-catalyzed asymmetric aldol reactions. Chemical Communications (Cambridge, England). 59: 8424-8427. PMID 37334826 DOI: 10.1039/d3cc01606d |
0.477 |
|
2023 |
Yasumoto K, Kunitomo N, Kano T. Cu-Catalyzed Asymmetric Alkenylation of Enone Diesters with Trialkenylboroxines. Organic Letters. 25: 1497-1502. PMID 36861961 DOI: 10.1021/acs.orglett.3c00262 |
0.367 |
|
2023 |
Tsuzuki S, Kano T. Asymmetric Synthesis of Chiral Sulfimides through the O-Alkylation of Enantioenriched Sulfinamides and Addition of Carbon Nucleophiles. Angewandte Chemie (International Ed. in English). 62: e202300637. PMID 36807500 DOI: 10.1002/anie.202300637 |
0.418 |
|
2023 |
Takeshima A, Kano T. Diethylzinc-Mediated Cross-Coupling Reactions between Dibromoketones and Monobromo Carbonyl Compounds. Angewandte Chemie (International Ed. in English). 62: e202217496. PMID 36583678 DOI: 10.1002/anie.202217496 |
0.347 |
|
2022 |
Golub TP, Kano T, Maruoka K, Merten C. VCD spectroscopy distinguishes the enamine and iminium ion of a 1,1'-binaphthyl azepine. Chemical Communications (Cambridge, England). PMID 35796225 DOI: 10.1039/d2cc02863h |
0.525 |
|
2022 |
Maeda Y, Hamada S, Aota Y, Otsubo K, Kano T, Maruoka K. Practical Asymmetric Synthesis of Chiral Sulfoximines via Sulfur-Selective Alkylation. The Journal of Organic Chemistry. PMID 35075904 DOI: 10.1021/acs.joc.1c02424 |
0.645 |
|
2021 |
Tsuzuki S, Sakurai S, Matsumoto A, Kano T, Maruoka K. Ni-Catalyzed C(sp)-H alkylation of -quinolylbenzamides using alkylsilyl peroxides as structurally diverse alkyl sources. Chemical Communications (Cambridge, England). PMID 34286742 DOI: 10.1039/d1cc02983e |
0.526 |
|
2021 |
Homma C, Kano T, Maruoka K. Bifunctional amino sulfonamide-catalyzed asymmetric conjugate addition to alkenyl alkynyl ketimines as enone surrogates. Chemical Communications (Cambridge, England). PMID 33600542 DOI: 10.1039/d0cc07842e |
0.659 |
|
2021 |
Inukai T, Kano T, Maruoka K. Asymmetric α-Hydroxylation of α-Aryl-δ-lactams with Molecular Oxygen under Phase-Transfer Conditions. Organic Letters. 23: 792-796. PMID 33476160 DOI: 10.1021/acs.orglett.0c04022 |
0.591 |
|
2020 |
Homma C, Takeshima A, Kano T, Maruoka K. Construction of chiral α--amine scaffolds amine-catalyzed asymmetric Mannich reactions of alkyl-substituted ketimines. Chemical Science. 12: 1445-1450. PMID 34163907 DOI: 10.1039/d0sc05269h |
0.696 |
|
2020 |
Sakurai S, Kano T, Maruoka K. Cu-Catalyzed -alkylation of phenol derivatives with alkylsilyl peroxides. Chemical Communications (Cambridge, England). PMID 33290475 DOI: 10.1039/d0cc07305a |
0.602 |
|
2020 |
Mochimatsu T, Aota Y, Kano T, Maruoka K. CuCl -Mediated Oxidative Intramolecular α-Arylation of Ketones with Phenolic Nucleophiles via Oxy-Allyl Cation Intermediates. Chemistry, An Asian Journal. PMID 33025747 DOI: 10.1002/asia.202001032 |
0.59 |
|
2020 |
Sakurai S, Matsumoto A, Kano T, Maruoka K. Cu-Catalyzed Enantioselective Alkylarylation of Vinylarenes Enabled by Chiral Binaphthyl-BOX Hybrid Ligands. Journal of the American Chemical Society. PMID 33017146 DOI: 10.1021/jacs.0c09008 |
0.669 |
|
2020 |
Yasumoto K, Kano T, Maruoka K. Synthesis of Electron-Deficient Chiral Biphenols and Their Applica-tions in Catalytic Asymmetric Reactions. The Journal of Organic Chemistry. PMID 32614186 DOI: 10.1021/Acs.Joc.0C01116 |
0.704 |
|
2020 |
Bai JF, Zhao L, Wang F, Yan F, Kano T, Maruoka K, Li Y. Organocatalytic Formal (3 + 2) Cycloaddition toward Chiral Pyrrolo[1,2-]indoles via Dynamic Kinetic Resolution of Allene Intermediates. Organic Letters. PMID 32598844 DOI: 10.1021/Acs.Orglett.0C01812 |
0.723 |
|
2020 |
Takeshima A, Shimogaki M, Kano T, Maruoka K. Development of Ketone-Based Brominating Agents (KBA) for the Practical Asymmetric α-Bromination of Aldehydes Catalyzed by Tritylpyrrolidine Acs Catalysis. 10: 5959-5963. DOI: 10.1021/Acscatal.0C01596 |
0.639 |
|
2020 |
Shimogaki M, Takeshima A, Kano T, Maruoka K. Front Cover: Enantioselective Synthesis of Monosaccharide Analogues by Two-Step Sequential Enamine Catalysis: Benzoyloxylation and Aldol Reaction (Eur. J. Org. Chem. 14/2020) European Journal of Organic Chemistry. 2020: 2005-2005. DOI: 10.1002/Ejoc.202000323 |
0.716 |
|
2020 |
Aota Y, Doko Y, Kano T, Maruoka K. Brønsted Acid-Catalyzed Intramolecular α-Arylation of Ketones with Phenolic Nucleophiles via Oxy-Allyl Cation Intermediates European Journal of Organic Chemistry. 2020: 1907-1911. DOI: 10.1002/Ejoc.202000169 |
0.677 |
|
2020 |
Shimogaki M, Takeshima A, Kano T, Maruoka K. Enantioselective Synthesis of Monosaccharide Analogues by Two-Step Sequential Enamine Catalysis: Benzoyloxylation and Aldol Reaction European Journal of Organic Chemistry. 2020: 2028-2032. DOI: 10.1002/Ejoc.202000073 |
0.724 |
|
2020 |
Inukai T, Kano T, Maruoka K. Inside Cover: Construction of Quaternary Carbon Center by Catalytic Asymmetric Alkylation of 3‐Arylpiperidin‐2‐ones Under Phase‐Transfer Conditions (Angew. Chem. Int. Ed. 6/2020) Angewandte Chemie International Edition. 59: 2126-2126. DOI: 10.1002/Anie.201915938 |
0.608 |
|
2019 |
Inukai T, Kano T, Maruoka K. Construction of a Chiral Quaternary Carbon Center by Catalytic Asymmetric Alkylation of 3-Arylpiperidin-2-ones under Phase-Transfer Conditions. Angewandte Chemie (International Ed. in English). PMID 31769914 DOI: 10.1002/Anie.201913518 |
0.7 |
|
2019 |
Aota Y, Kano T, Maruoka K. Asymmetric synthesis of chiral sulfoximines via the S-arylation of sulfinamides. Journal of the American Chemical Society. PMID 31739663 DOI: 10.1021/Jacs.9B11298 |
0.708 |
|
2019 |
Aota Y, Maeda Y, Kano T, Maruoka K. Efficient Synthesis of Cyclic Sulfoximines from N-Propargylsulfinamides via Sulfur-Carbon Bond Formation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31573124 DOI: 10.1002/Chem.201904501 |
0.681 |
|
2019 |
Aota Y, Kano T, Maruoka K. Asymmetric Synthesis of Chiral Sulfoximines via the S-Alkylation of Sulfinamides. Angewandte Chemie (International Ed. in English). PMID 31568618 DOI: 10.1002/Anie.201911021 |
0.713 |
|
2019 |
Takeshima A, Kano T, Maruoka K. Synthesis of Phenylcyclopropane-Based Secondary Amine Catalysts and Their Applications in Enamine Catalysis. Organic Letters. PMID 31513419 DOI: 10.1021/Acs.Orglett.9B03070 |
0.738 |
|
2019 |
Bai JF, Yasumoto K, Kano T, Maruoka K. Asymmetric Synthesis of Chiral 1,4-Enynes via Organocatalytic Alkenylation of Propargyl Alcohols with Trialkenylboroxines. Angewandte Chemie (International Ed. in English). PMID 31056810 DOI: 10.1002/Anie.201904520 |
0.708 |
|
2019 |
Yasumoto K, Kano T, Maruoka K. One-Pot Synthesis of Less Accessible N-Boc-Propargylic Amines through BF-Catalyzed Alkynylation and Allylation Using Boronic Esters. Organic Letters. PMID 30983369 DOI: 10.1021/Acs.Orglett.9B00931 |
0.678 |
|
2019 |
Inukai T, Kano T, Maruoka K. Innentitelbild: Construction of Quaternary Carbon Center by Catalytic Asymmetric Alkylation of 3‐Arylpiperidin‐2‐ones Under Phase‐Transfer Conditions (Angew. Chem. 6/2020) Angewandte Chemie. 132: 2146-2146. DOI: 10.1002/Ange.201915938 |
0.615 |
|
2018 |
Bai JF, Yasumoto K, Kano T, Maruoka K. Synthesis of 1-aminoindenes through aza-Prins-type cyclization. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29802655 DOI: 10.1002/Chem.201802448 |
0.709 |
|
2018 |
Kano T, Maruyama H, Homma C, Maruoka K. Catalyst-controlled diastereoselectivity reversal in the formation of dihydropyrans. Chemical Communications (Cambridge, England). PMID 29564425 DOI: 10.1039/C8Cc01443D |
0.663 |
|
2018 |
Kano T, Yasumoto K, Maruoka K. BF3
-Catalyzed Synthesis of Cyclic Carbamates from Boc-Protected Aminals and Alkynes Asian Journal of Organic Chemistry. 7: 1575-1578. DOI: 10.1002/Ajoc.201800289 |
0.686 |
|
2017 |
Kano T, Maruyama H, Homma C, Maruoka K. Chiral amine-catalyzed asymmetric conjugate addition of aldehydes to α-phenylselenoenones as formal Z-allylating agents. Chemical Communications (Cambridge, England). PMID 29218335 DOI: 10.1039/C7Cc08691A |
0.7 |
|
2017 |
Kano T, Aota Y, Maruoka K. Asymmetric Synthesis of Less Accessible α-Tertiary Amines from Alkynyl Z-Ketimines. Angewandte Chemie (International Ed. in English). PMID 29110376 DOI: 10.1002/Anie.201710084 |
0.679 |
|
2017 |
Shimogaki M, Maruyama H, Tsuji S, Homma C, Kano T, Maruoka K. Synthesis of Chiral Tritylpyrrolidine Derivatives and Their Application to Asymmetric Benzoyloxylation. The Journal of Organic Chemistry. PMID 29092400 DOI: 10.1021/Acs.Joc.7B02562 |
0.667 |
|
2017 |
Bai JF, Sasagawa H, Yurino T, Kano T, Maruoka K. In situ generation of N-Boc-protected alkenyl imines: controlling the E/Z geometry of alkenyl moieties in the Mukaiyama-Mannich reaction. Chemical Communications (Cambridge, England). PMID 28681883 DOI: 10.1039/C7Cc04674J |
0.671 |
|
2017 |
Kan J, Maruyama H, Akakura M, Kano T, Maruoka K. Catalyst-Controlled, Enantioselective and Diastereodivergent Conjugate Addition of Aldehydes to Electron-Deficient Olefins. Angewandte Chemie (International Ed. in English). PMID 28632909 DOI: 10.1002/Anie.201705546 |
0.636 |
|
2017 |
Kano T, Homma C, Maruoka K. In situ generation of less accessible Boc-imines from aldehydes: construction of a quaternary carbon by the Mannich reaction or unprecedented aldol reaction. Organic & Biomolecular Chemistry. PMID 28513717 DOI: 10.1039/C7Ob01126A |
0.692 |
|
2016 |
Kano T, Kobayashi R, Maruoka K. Synthesis of N-Boc-Propargylic and Allylic Amines by Reaction of Organomagnesium Reagents with N-Boc-Aminals and Their Oxidation to N-Boc-Ketimines. Organic Letters. PMID 26727389 DOI: 10.1021/Acs.Orglett.5B03446 |
0.606 |
|
2016 |
Yurino T, Aota Y, Asakawa D, Kano T, Maruoka K. N-Boc-aminals as easily accessible precursors for less accessible N-Boc-imines: facile synthesis of optically active propargylamine derivatives using Mannich-type reactions Tetrahedron. 72: 3687-3700. DOI: 10.1016/J.Tet.2016.03.076 |
0.694 |
|
2016 |
Yurino T, Aota Y, Asakawa D, Kano T, Maruoka K. ChemInform Abstract: N-Boc-Aminals as Easily Accessible Precursors for Less Accessible N-Boc-Imines: Facile Synthesis of Optically Active Propargylamine Derivatives Using Mannich-Type Reactions. Cheminform. 47. DOI: 10.1002/chin.201641058 |
0.613 |
|
2016 |
Kano T, Aota Y, Asakawa D, Maruoka K. ChemInform Abstract: Broensted Acid-Catalyzed Mannich Reaction Through Dual Activation of Aldehydes and N-Boc-imines. Cheminform. 47: no-no. DOI: 10.1002/chin.201611092 |
0.646 |
|
2016 |
Kano T, Aota Y, Maruoka K. Rate Acceleration of Solid-Liquid Phase-Transfer Catalysis by Rotor-Stator Homogenizer Advanced Synthesis & Catalysis. 358: 2996-2999. DOI: 10.1002/Adsc.201600425 |
0.574 |
|
2015 |
Kano T, Aota Y, Asakawa D, Maruoka K. Brønsted acid-catalyzed Mannich reaction through dual activation of aldehydes and N-Boc-imines. Chemical Communications (Cambridge, England). PMID 26412495 DOI: 10.1039/C5Cc07290E |
0.71 |
|
2015 |
Kano T, Sugimoto H, Maruyama H, Maruoka K. Regio- and Stereoselective Conjugate Addition of Aldehydes to β-Tosyl Enones under the Catalysis of a Binaphthyl-Modified Chiral Amine. Angewandte Chemie (International Ed. in English). 54: 8462-5. PMID 26089137 DOI: 10.1002/Anie.201500225 |
0.699 |
|
2015 |
Kano T, Kobayashi R, Maruoka K. Versatile In Situ Generated N-Boc-Imines: Application to Phase-Transfer-Catalyzed Asymmetric Mannich-Type Reactions. Angewandte Chemie (International Ed. in English). 54: 8471-4. PMID 26068918 DOI: 10.1002/Anie.201502215 |
0.676 |
|
2015 |
Kano T, Maruyama H, Sakamoto R, Maruoka K. Regioselectivity switch in chiral amine-catalysed asymmetric addition of aldehydes to reactive enals. Chemical Communications (Cambridge, England). 51: 10062-5. PMID 26006325 DOI: 10.1039/C5Cc02438B |
0.729 |
|
2014 |
Kano T, Takeda M, Sakamoto R, Maruoka K. Synthesis of 3-mono-substituted binaphthyl-based secondary amine catalysts via monobromination of an axially chiral dicarboxylic acid derivative. The Journal of Organic Chemistry. 79: 4240-4. PMID 24708270 DOI: 10.1021/Jo500637Q |
0.73 |
|
2014 |
Kano T, Shirozu F, Maruoka K. Practical approach for asymmetric hydroxyamination of aldehydes with in situ generated nitrosocarbonyl compounds: application to one-pot synthesis of chiral allylamines. Organic Letters. 16: 1530-2. PMID 24552183 DOI: 10.1021/Ol5000742 |
0.705 |
|
2014 |
Kano T, Sakamoto R, Maruoka K. Amine-catalyzed asymmetric cross-aldol reactions using heterofunctionalized acetaldehydes as nucleophiles. Organic Letters. 16: 944-7. PMID 24428414 DOI: 10.1021/Ol4036837 |
0.699 |
|
2014 |
Kano T, Takechi R, Kobayashi R, Maruoka K. Chiral Brønsted acid-catalyzed enantioselective addition of indoles to ketimines. Organic & Biomolecular Chemistry. 12: 724-7. PMID 24323293 DOI: 10.1039/C3Ob42190B |
0.731 |
|
2014 |
Kano T, Sakamoto R, Maruoka K. Remote chirality control based on the organocatalytic asymmetric Mannich reaction of α-thio acetaldehydes. Chemical Communications (Cambridge, England). 50: 942-4. PMID 24305743 DOI: 10.1039/C3Cc47827K |
0.702 |
|
2014 |
Kano T, Maruyama H, Akiyama K, Maruoka K. Design and synthesis of a biphenyl-based chiral amino sulfonamide with high catalytic performance in Mannich reactions Tetrahedron Letters. 55: 4227-4229. DOI: 10.1016/J.Tetlet.2014.05.049 |
0.717 |
|
2013 |
Nakamura T, Harachi M, Kano T, Mukaeda Y, Hosokawa S. Concise synthesis of reduced propionates by stereoselective reductions combined with the Kobayashi reaction. Organic Letters. 15: 3170-3. PMID 24490779 DOI: 10.1021/ol401406m |
0.451 |
|
2013 |
Kano T, Shirozu F, Maruoka K. Metal-free enantioselective hydroxyamination of aldehydes with nitrosocarbonyl compounds catalyzed by an axially chiral amine. Journal of the American Chemical Society. 135: 18036-9. PMID 24215509 DOI: 10.1021/Ja4099627 |
0.676 |
|
2013 |
Kano T, Yurino T, Maruoka K. Organocatalytic asymmetric synthesis of propargylamines with two adjacent stereocenters: mannich-type reactions of in situ generated C-alkynyl imines with β-keto esters. Angewandte Chemie (International Ed. in English). 52: 11509-12. PMID 24038946 DOI: 10.1002/Anie.201304963 |
0.748 |
|
2013 |
Kano T, Sugimoto H, Tokuda O, Maruoka K. Unusual anti-selective asymmetric conjugate addition of aldehydes to nitroalkenes catalyzed by a biphenyl-based chiral secondary amine. Chemical Communications (Cambridge, England). 49: 7028-30. PMID 23660992 DOI: 10.1039/C3Cc42488J |
0.695 |
|
2013 |
Kano T, Hayashi Y, Maruoka K. Construction of a chiral quaternary carbon center by catalytic asymmetric alkylation of 2-arylcyclohexanones under phase-transfer conditions. Journal of the American Chemical Society. 135: 7134-7. PMID 23634801 DOI: 10.1021/Ja403340R |
0.679 |
|
2013 |
Kano T, Yurino T, Asakawa D, Maruoka K. Acid-catalyzed in situ generation of less accessible or unprecedented N-Boc imines from N-Boc aminals. Angewandte Chemie (International Ed. in English). 52: 5532-4. PMID 23589439 DOI: 10.1002/Anie.201300231 |
0.597 |
|
2013 |
Kano T, Sakamoto R, Yamaguchi Y, Itoh K, Maruoka K. One-pot cross double-Mannich reaction of acetaldehyde catalyzed by a binaphthyl-based amino sulfonamide. Chemical Communications (Cambridge, England). 49: 1118-20. PMID 23282574 DOI: 10.1039/C2Cc38370E |
0.721 |
|
2013 |
Kano T, Kumano T, Sakamoto R, Maruoka K. Stereoselective synthesis of cyclic amino acids via asymmetric phase-transfer catalytic alkylation. Organic & Biomolecular Chemistry. 11: 271-8. PMID 23076259 DOI: 10.1039/C2Ob26778K |
0.682 |
|
2013 |
Kano T, Maruoka K. Unique properties of chiral biaryl-based secondary amine catalysts for asymmetric enamine catalysis Chemical Science. 4: 907-915. DOI: 10.1039/C2Sc21612D |
0.708 |
|
2012 |
Kano T, Shirozu F, Akakura M, Maruoka K. Powerful amino diol catalyst for effecting the direct asymmetric conjugate addition of aldehydes to acrylates. Journal of the American Chemical Society. 134: 16068-73. PMID 22950545 DOI: 10.1021/Ja307668B |
0.737 |
|
2012 |
Kano T, Song S, Maruoka K. Molecular recognition of ketomalonates by asymmetric aldol reaction of aldehydes with secondary-amine organocatalysts. Chemical Communications (Cambridge, England). 48: 7037-9. PMID 22684237 DOI: 10.1039/C2Cc32772D |
0.734 |
|
2012 |
Kano T, Sakamoto R, Akakura M, Maruoka K. Stereocontrolled synthesis of vicinal diamines by organocatalytic asymmetric Mannich reaction of N-protected aminoacetaldehydes: formal synthesis of (-)-agelastatin A. Journal of the American Chemical Society. 134: 7516-20. PMID 22486203 DOI: 10.1021/Ja301120Z |
0.746 |
|
2012 |
Kano T, Song S, Kubota Y, Maruoka K. Highly diastereo- and enantioselective Mannich reactions of synthetically flexible ketimines with secondary amine organocatalysts. Angewandte Chemie (International Ed. in English). 51: 1191-4. PMID 22173941 DOI: 10.1002/Anie.201107375 |
0.71 |
|
2011 |
Kano T, Sugimoto H, Maruoka K. Efficient organocatalytic cross-aldol reaction between aliphatic aldehydes through their functional differentiation. Journal of the American Chemical Society. 133: 18130-3. PMID 21999103 DOI: 10.1021/Ja208873K |
0.722 |
|
2011 |
Kano T, Noishiki A, Sakamoto R, Maruoka K. syn-Selective asymmetric cross-aldol reactions between aldehydes and glyoxylic acid derivatives catalyzed by an axially chiral amino sulfonamide. Chemical Communications (Cambridge, England). 47: 10626-8. PMID 21892467 DOI: 10.1039/C1Cc14347F |
0.724 |
|
2011 |
Kano T, Yamamoto A, Song S, Maruoka K. Catalytic asymmetric syntheses of isoxazoline-N-oxides under phase-transfer conditions. Chemical Communications (Cambridge, England). 47: 4358-60. PMID 21286641 DOI: 10.1039/C0Cc05786J |
0.609 |
|
2011 |
Kano T, Yamamoto A, Song S, Maruoka K. Catalytic asymmetric synthesis of isoxazoline-n-oxides through conjugate additioncyclization under phase-transfer conditions Bulletin of the Chemical Society of Japan. 84: 1057-1065. DOI: 10.1246/Bcsj.20110155 |
0.631 |
|
2011 |
Kano T, Shirozu F, Tatsumi K, Kubota Y, Maruoka K. The first example of the direct asymmetric conjugate addition of aldehydes to a methylenemalonate promoted by an axially chiral amino diol catalyst Chemical Science. 2: 2311-2313. DOI: 10.1039/C1Sc00453K |
0.727 |
|
2010 |
Kano T, Shirozu F, Maruoka K. Direct asymmetric bromination of aldehydes catalyzed by a binaphthyl-based secondary amine: highly enantio- and diastereoselective one-pot synthesis of bromohydrins. Chemical Communications (Cambridge, England). 46: 7590-2. PMID 20830441 DOI: 10.1039/C0Cc02739A |
0.737 |
|
2010 |
Kano T, Mii H, Maruoka K. Metal-free direct asymmetric aminoxylation of aldehydes catalyzed by a binaphthyl-based chiral amine. Angewandte Chemie (International Ed. in English). 49: 6638-41. PMID 20672271 DOI: 10.1002/Anie.201002965 |
0.647 |
|
2010 |
Kano T, Maruoka K. Development of highly selective organic reactions catalyzed by designed amine organocatalysts Bulletin of the Chemical Society of Japan. 83: 1421-1438. DOI: 10.1246/Bcsj.20100229 |
0.702 |
|
2010 |
Maruoka K, Kano T, Mii H. Organocatalytic Asymmetric α-Aminoxylation of Aldehydes Synfacts. 2010: 1192-1192. DOI: 10.1055/S-0030-1258677 |
0.551 |
|
2010 |
Kano T, Kumano T, Sakamoto R, Maruoka K. Catalytic asymmetric synthesis of cyclic amino acids and alkaloid derivatives: Application to (+)-dihydropinidine and Selfotel synthesis Chemical Science. 1: 499-501. DOI: 10.1039/C0Sc00250J |
0.674 |
|
2010 |
Kano T, Sakamoto R, Mii H, Wang YG, Maruoka K. Catalytic asymmetric synthesis of cyclic α-alkyl-amino acid derivatives by C,N-double alkylation Tetrahedron. 66: 4900-4904. DOI: 10.1016/J.Tet.2010.01.105 |
0.665 |
|
2010 |
Saito S, Kano T, Muto H, Nakadai M, Yamamoto H. ChemInform Abstract: Asymmetric Coupling of Phenols with Arylleads. Cheminform. 31: no-no. DOI: 10.1002/chin.200001108 |
0.492 |
|
2009 |
Kano T, Yamaguchi Y, Maruoka K. A designer axially chiral amino sulfonamide as an efficient organocatalyst for direct asymmetric anti-selective Mannich reactions and syn-selective cross-aldol reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 6678-87. PMID 19479934 DOI: 10.1002/Chem.200900267 |
0.719 |
|
2009 |
Ueda M, Kano T, Maruoka K. Organocatalyzed direct asymmetric alpha-halogenation of carbonyl compounds. Organic & Biomolecular Chemistry. 7: 2005-12. PMID 19421434 DOI: 10.1039/B901449G |
0.602 |
|
2009 |
Wang YG, Mii H, Kano T, Maruoka K. Catalytic asymmetric synthesis of cyclic alpha-alkyl-amino acid derivatives having a tetrasubstituted alpha-carbon. Bioorganic & Medicinal Chemistry Letters. 19: 3795-7. PMID 19406639 DOI: 10.1016/J.Bmcl.2009.04.025 |
0.611 |
|
2009 |
Kano T, Kumano T, Maruoka K. Rate enhancement of phase transfer catalyzed conjugate additions by CsCl. Organic Letters. 11: 2023-5. PMID 19348469 DOI: 10.1021/Ol900476E |
0.645 |
|
2009 |
Wang YG, Kumano T, Kano T, Maruoka K. Organocatalytic approach to enantioselective one-pot synthesis of pyrrolidine, hexahydropyrrolizine, and octahydroindolizine core structures. Organic Letters. 11: 2027-9. PMID 19348468 DOI: 10.1021/Ol900477X |
0.681 |
|
2009 |
Kano T, Tanaka Y, Osawa K, Yurino T, Maruoka K. Catalytic enantioselective construction of all-carbon quaternary stereocenters by an organocatalytic Diels-Alder reaction of alpha-substituted alpha,beta-unsaturated aldehydes. Chemical Communications (Cambridge, England). 1956-8. PMID 19333455 DOI: 10.1039/B819034H |
0.614 |
|
2009 |
Kano T, Mii H, Maruoka K. Direct asymmetric benzoyloxylation of aldehydes catalyzed by 2-tritylpyrrolidine. Journal of the American Chemical Society. 131: 3450-1. PMID 19227974 DOI: 10.1021/Ja809963S |
0.651 |
|
2009 |
Kano T, Yamaguchi Y, Maruoka K. A designer axially chiral amino sulfonamide as an efficient organocatalyst for direct asymmetric mannich reactions of N-Boc-protected imines. Angewandte Chemie (International Ed. in English). 48: 1838-40. PMID 19173354 DOI: 10.1002/Anie.200805628 |
0.73 |
|
2009 |
Kano T, Yamamoto A, Shirozu F, Maruoka K. Enantioselectivity switch in direct asymmetric aminoxylation catalyzed by binaphthyl-based chiral secondary amines Synthesis. 1557-1563. DOI: 10.1055/S-0029-1216635 |
0.686 |
|
2009 |
Wang Y, Mii H, Kano T, Maruoka K. ChemInform Abstract: Catalytic Asymmetric Synthesis of Cyclic α-Alkyl-amino Acid Derivatives Having a Tetrasubstituted α-Carbon. Cheminform. 40: no-no. DOI: 10.1002/chin.200948189 |
0.611 |
|
2009 |
Ueda M, Kano T, Maruoka K. ChemInform Abstract: Organocatalyzed Direct Asymmetric α-Halogenation of Carbonyl Compounds Cheminform. 40. DOI: 10.1002/chin.200936227 |
0.531 |
|
2009 |
Kano T, Tanaka Y, Osawa K, Yurino T, Maruoka K. ChemInform Abstract: Catalytic Enantioselective Construction of All-Carbon Quaternary Stereocenters by an Organocatalytic Diels-Alder Reaction of α-Substituted α,β-Unsaturated Aldehydes. Cheminform. 40. DOI: 10.1002/chin.200935066 |
0.61 |
|
2008 |
Kano T, Maruoka K. Design of chiral bifunctional secondary amine catalysts for asymmetric enamine catalysis. Chemical Communications (Cambridge, England). 5465-73. PMID 18997926 DOI: 10.1039/B809301F |
0.706 |
|
2008 |
Kano T, Tanaka Y, Osawa K, Yurino T, Maruoka K. Facile synthesis of structurally diverse 3,3'-disubstituted 1,1'-binaphthyl-2,2'-diamines in optically pure forms. The Journal of Organic Chemistry. 73: 7387-9. PMID 18702550 DOI: 10.1021/Jo8011368 |
0.63 |
|
2008 |
Kano T, Ueda M, Maruoka K. Direct asymmetric iodination of aldehydes using an axially chiral bifunctional amino alcohol catalyst. Journal of the American Chemical Society. 130: 3728-9. PMID 18321093 DOI: 10.1021/Ja074003O |
0.7 |
|
2008 |
Hashimoto T, Omote M, Hato Y, Kano T, Maruoka K. Asymmetric 1,3-dipolar cycloadditions of N-benzyl and N-diphenylmethyl nitrones and alpha,beta-unsaturated aldehydes catalyzed by bis-titanium chiral Lewis acids. Chemistry, An Asian Journal. 3: 407-12. PMID 18203215 DOI: 10.1002/Asia.200700344 |
0.662 |
|
2008 |
Kano T, Yamamoto A, Mu H, Takai J, Shirakawa S, Maruoka K. Direct asymmetric aminoxylation reaction catalyzed by axially chiral amino acids Chemistry Letters. 37: 250-251. DOI: 10.1246/Cl.2008.250 |
0.71 |
|
2008 |
Kano T, Yamamoto A, Maruoka K. Direct asymmetric aminoxylation reaction catalyzed by a binaphthyl-based chiral amino sulfonamide with high catalytic performance Tetrahedron Letters. 49: 5369-5371. DOI: 10.1016/J.Tetlet.2008.06.093 |
0.737 |
|
2008 |
Kano T, Hato Y, Yamamoto A, Maruoka K. anti-Selective direct asymmetric Mannich reactions catalyzed by chiral pyrrolidine-based amino sulfonamides Tetrahedron. 64: 1197-1203. DOI: 10.1016/J.Tet.2007.11.086 |
0.67 |
|
2007 |
Hashimoto T, Naganawa Y, Kano T, Maruoka K. Construction of stereodefined 1,1,2,2-tetrasubstituted cyclopropanes by acid catalyzed reaction of aryldiazoacetates and alpha-substituted acroleins. Chemical Communications (Cambridge, England). 5143-5. PMID 18060122 DOI: 10.1039/B715803C |
0.638 |
|
2007 |
Hashimoto T, Omote M, Kano T, Maruoka K. Asymmetric 1,3-dipolar cycloadditions of nitrones and methacrolein catalyzed by chiral bis-titanium lewis acid: a dramatic effect of N-substituent on nitrone. Organic Letters. 9: 4805-8. PMID 17929826 DOI: 10.1021/Ol702123N |
0.697 |
|
2007 |
Kano T, Tanaka Y, Maruoka K. exo-Selective asymmetric Diels-Alder reaction catalyzed by diamine salts as organocatalysts. Chemistry, An Asian Journal. 2: 1161-5. PMID 17640000 DOI: 10.1002/Asia.200700122 |
0.717 |
|
2007 |
Maruoka K, Ooi T, Kano T. Design of chiral organocatalysts for practical asymmetric synthesis of amino acid derivatives. Chemical Communications (Cambridge, England). 1487-95. PMID 17406684 DOI: 10.1039/B613049F |
0.764 |
|
2007 |
Kano T, Yamaguchi Y, Tanaka Y, Maruoka K. syn-selective and enantioselective direct cross-aldol reactions between aldehydes catalyzed by an axially chiral amino sulfonamide. Angewandte Chemie (International Ed. in English). 46: 1738-40. PMID 17397089 DOI: 10.1002/Anie.200604640 |
0.731 |
|
2007 |
Maruoka K, Kano T, Yamaguchi Y, Tanaka Y. syn-Selective Direct Asymmetric Cross-Aldol Reaction Synfacts. 2007: 0429-0429. DOI: 10.1055/s-2007-968351 |
0.614 |
|
2007 |
Tambar UK, Kano T, Zepernick JF, Stoltz BM. The development and scope of a versatile tandem Stille-oxa-electrocyclization reaction Tetrahedron Letters. 48: 345-350. DOI: 10.1016/J.Tetlet.2006.11.097 |
0.771 |
|
2007 |
Kano T, Tanaka Y, Maruoka K. Asymmetric organocatalytic oxy-Michael addition of alcohols to α,β-unsaturated aldehydes Tetrahedron. 63: 8658-8664. DOI: 10.1016/J.Tet.2007.03.179 |
0.651 |
|
2007 |
Tambar UK, Kano T, Zepernick JF, Stoltz BM. Convergent and Diastereoselective Synthesis of the Polycyclic Pyran Core (I) of Saudin (II). Cheminform. 38. DOI: 10.1002/chin.200710200 |
0.448 |
|
2007 |
Kano T, Lan Q, Wang X, Maruoka K. Effects of aromatic substituents on binaphthyl-based chiral spiro-type ammonium salts in asymmetric phase-transfer reactions Advanced Synthesis and Catalysis. 349: 556-560. DOI: 10.1002/Adsc.200600576 |
0.706 |
|
2006 |
Kano T, Tokuda O, Takai J, Maruoka K. Design of a binaphthyl-based axially chiral amino acid as an organocatalyst for direct asymmetric aldol reactions. Chemistry, An Asian Journal. 1: 210-5. PMID 17441057 DOI: 10.1002/Asia.200600077 |
0.73 |
|
2006 |
Tambar UK, Kano T, Zepernick JF, Stoltz BM. Convergent and diastereoselective synthesis of the polycyclic pyran core of saudin. The Journal of Organic Chemistry. 71: 8357-64. PMID 17064005 DOI: 10.1021/Jo061236+ |
0.729 |
|
2006 |
Kano T, Tanaka Y, Maruoka K. exo-selective asymmetric Diels-Alder reaction catalyzed by diamine salts as organocatalysts. Organic Letters. 8: 2687-9. PMID 16774232 DOI: 10.1021/Ol060621I |
0.656 |
|
2006 |
Kano T, Ueda M, Takai J, Maruoka K. Direct asymmetric hydroxyamination reaction catalyzed by an axially chiral secondary amine catalyst. Journal of the American Chemical Society. 128: 6046-7. PMID 16669668 DOI: 10.1021/Ja0604515 |
0.724 |
|
2006 |
Kano T, Hashimoto T, Maruoka K. Enantioselective 1,3-dipolar cycloaddition reaction between diazoacetates and alpha-substituted acroleins: total synthesis of manzacidin A. Journal of the American Chemical Society. 128: 2174-5. PMID 16478146 DOI: 10.1021/Ja056851U |
0.715 |
|
2006 |
Maruoka K, Kano T, Tanaka Y. Chiral Diamine-Salts for Catalytic exo-selective Diels-Alder Reactions Synfacts. 2006: 0843-0843. DOI: 10.1055/s-2006-942025 |
0.688 |
|
2006 |
Maruoka K, Kano T, Hashimoto T. Synthesis of Manzacidin A Synfacts. 2006: 0645-0645. DOI: 10.1055/S-2006-941828 |
0.581 |
|
2006 |
Maruoka K, Kano T, Ueda M, Takai J. Enamine Catalysis for the Direct Asymmetric Hydroxyamination Synfacts. 2006: 0615-0615. DOI: 10.1055/S-2006-941780 |
0.6 |
|
2006 |
Maruoka K, Kano T, Konishi T, Konishi S. Sn(IV)-Catalyzed Asymmetric Acrolein Diels-Alder Reaction Synfacts. 2006: 0468-0468. DOI: 10.1055/S-2006-934347 |
0.644 |
|
2006 |
Kano T, Hato Y, Maruoka K. Design of a C2-symmetric chiral pyrrolidine-based amino sulfonamide: application to anti-selective direct asymmetric Mannich reactions Tetrahedron Letters. 47: 8467-8469. DOI: 10.1016/J.Tetlet.2006.09.147 |
0.677 |
|
2006 |
Kano T, Tokuda O, Maruoka K. Synthesis of a biphenyl-based axially chiral amino acid as a highly efficient catalyst for the direct asymmetric aldol reaction Tetrahedron Letters. 47: 7423-7426. DOI: 10.1016/J.Tetlet.2006.08.051 |
0.739 |
|
2006 |
Kano T, Sasaki K, Konishi T, Mii H, Maruoka K. Highly efficient trialkylsilylcyanation of aldehydes, ketones and imines catalyzed by a nucleophilic N-heterocyclic carbene Tetrahedron Letters. 47: 4615-4618. DOI: 10.1016/J.Tetlet.2006.04.141 |
0.711 |
|
2006 |
Kano T, Tanaka Y, Maruoka K. Organocatalytic oxy-Michael addition of alcohols to α,β-unsaturated aldehydes Tetrahedron Letters. 47: 3039-3041. DOI: 10.1016/j.tetlet.2006.03.001 |
0.506 |
|
2006 |
Kano T, Tanaka Y, Maruoka K. Organocatalytic Oxy-Michael Addition of Alcohols to α,β-Unsaturated Aldehydes. Cheminform. 37. DOI: 10.1016/J.Tetlet.2006.03.001 |
0.595 |
|
2006 |
Kano T, Konishi T, Konishi S, Maruoka K. Design of chiral tin(IV) aryloxide as a mild Lewis acid catalyst for enantioselective Diels-Alder reaction Tetrahedron Letters. 47: 873-875. DOI: 10.1016/J.Tetlet.2005.12.001 |
0.726 |
|
2006 |
Ooi T, Arimura Y, Hiraiwa Y, Yuan LM, Kano T, Inoue T, Matsumoto J, Maruoka K. Highly enantioselective monoalkylation of p-chlorobenzaldehyde imine of glycine tert-butyl ester under mild phase-transfer conditions Tetrahedron Asymmetry. 17: 603-606. DOI: 10.1016/J.Tetasy.2006.01.019 |
0.823 |
|
2006 |
Kano T, Sasaki K, Konishi T, Mii H, Maruoka K. Highly Efficient Trialkylsilylcyanation of Aldehydes, Ketones and Imines Catalyzed by a Nucleophilic N-Heterocyclic Carbene. Cheminform. 37. DOI: 10.1002/chin.200641046 |
0.638 |
|
2006 |
Ooi T, Arimura Y, Hiraiwa Y, Yuan LM, Kano T, Inoue T, Matsumoto J, Maruoka K. Highly Enantioselective Monoalkylation of p-Chlorobenzaldehyde Imine of Glycine tert-Butyl Ester under Mild Phase-Transfer Conditions. Cheminform. 37. DOI: 10.1002/chin.200632075 |
0.766 |
|
2006 |
Kano T. Asymmetric reactions catalyzed by chiral brøsted acids Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry. 64: 1075-1076. |
0.505 |
|
2005 |
Kano T, Yamaguchi Y, Tokuda O, Maruoka K. anti-selective direct asymmetric Mannich reactions catalyzed by axially chiral amino sulfonamide as an organocatalyst. Journal of the American Chemical Society. 127: 16408-9. PMID 16305223 DOI: 10.1021/Ja056008W |
0.727 |
|
2005 |
Tokuda O, Kano T, Gao WG, Ikemoto T, Maruoka K. A practical synthesis of (S)-2-cyclohexyl-2-phenylglycolic acid via organocatalytic asymmetric construction of a tetrasubstituted carbon center. Organic Letters. 7: 5103-5. PMID 16235968 DOI: 10.1021/Ol052164W |
0.707 |
|
2005 |
Kano T, Hashimoto T, Maruoka K. Asymmetric 1,3-dipolar cycloaddition reaction of nitrones and acrolein with a bis-titanium catalyst as chiral Lewis acid. Journal of the American Chemical Society. 127: 11926-7. PMID 16117516 DOI: 10.1021/Ja0523284 |
0.717 |
|
2005 |
Tambar UK, Kano T, Stoltz BM. Progress toward the total synthesis of saudin: development of a tandem Stille-oxa-electrocyclization reaction. Organic Letters. 7: 2413-6. PMID 15932211 DOI: 10.1021/Ol050705B |
0.778 |
|
2005 |
Kano T, Takai J, Tokuda O, Maruoka K. Design of an axially chiral amino acid with a binaphthyl backbone as an organocatalyst for a direct asymmetric aldol reaction. Angewandte Chemie (International Ed. in English). 44: 3055-7. PMID 15828036 DOI: 10.1002/Anie.200500408 |
0.696 |
|
2005 |
Kano T, Sasaki K, Maruoka K. Enantioselective acylation of secondary alcohols catalyzed by chiral N-heterocyclic carbenes. Organic Letters. 7: 1347-9. PMID 15787503 DOI: 10.1021/Ol050174R |
0.679 |
|
2005 |
Maruoka K, Kano T, Yamaguchi Y, Tokuda O. Organocatalyticanti-Selective Direct Mannich Reaction Synfacts. 2006: 0074-0074. DOI: 10.1055/S-2005-921709 |
0.594 |
|
2004 |
Kano T, Konishi S, Shirakawa S, Maruoka K. Design of new polyamine-based chiral phase-transfer catalysts for the enantioselective synthesis of phenylalanine Tetrahedron Asymmetry. 15: 1243-1245. DOI: 10.1016/j.tetasy.2004.02.023 |
0.633 |
|
2004 |
Kano T, Konishi S, Shirakawa S, Maruoka K. Design of New Polyamine-Based Chiral Phase-Transfer Catalysts for the Enantioselective Synthesis of Phenylalanine. Cheminform. 35. DOI: 10.1016/J.Tetasy.2004.02.023 |
0.673 |
|
2002 |
Kano T, Ohyabu Y, Saito S, Yamamoto H. Asymmetric carbon-carbon coupling of phenols or anilines with aryllead triacetates. Journal of the American Chemical Society. 124: 5365-73. PMID 11996577 DOI: 10.1021/Ja012287L |
0.615 |
|
2001 |
Stoltz BM, Kano T, Corey EJ. ChemInform Abstract: Enantioselective Total Synthesis of Nicandrenones. Cheminform. 32: no-no. DOI: 10.1002/chin.200101189 |
0.588 |
|
2000 |
Saito S, Kano T, Ohyabu Y, Yamamoto H. Direct coupling of anilines with aryllead triacetates Synlett. 1676-1678. DOI: 10.1055/S-2000-7916 |
0.505 |
|
2000 |
Stoltz BM, Kano T, Corey EJ. Enantioselective total synthesis of nicandrenones [10] Journal of the American Chemical Society. 122: 9044-9045. DOI: 10.1021/Ja0024892 |
0.522 |
|
1999 |
Saito S, Kano T, Muto H, Nakadai M, Yamamoto H. Asymmetric coupling of phenols with arylleads [2] Journal of the American Chemical Society. 121: 8943-8944. DOI: 10.1021/Ja990646V |
0.581 |
|
1999 |
Saito S, Hatanaka K, Kano T, Yamamoto H. Diastereoselective aldol reaction with an acetate enolate: 2,6-Bis(2- isopropylphenyl)-3,5-dimethylphenol as an extremely effective chiral auxiliary Angewandte Chemie - International Edition. 37: 3378-3381. DOI: 10.1002/(SICI)1521-3773(19981231)37:24<3378::AID-ANIE3378>3.0.CO;2-L |
0.717 |
|
1998 |
Saito S, Hatanaka K, Kano T, Yamamoto H. Diastereoselective Aldol Reaction with an Acetate Enolate: 2,6-Bis(2-isopropylphenyl)-3,5-dimethylphenol as an Extremely Effective Chiral Auxiliary. Angewandte Chemie (International Ed. in English). 37: 3378-3381. PMID 29711286 DOI: 10.1002/(Sici)1521-3773(19981231)37:24<3378::Aid-Anie3378>3.0.Co;2-L |
0.725 |
|
1998 |
Saito S, Hatanaka K, Kano T, Yamamoto H. Diastereoselektive Aldolreaktion mit einem Acetat-Enolat: 2,6-Bis(2-isopropylphenyl)-3,5-dimethylphenol als äußerst effektives chirales Auxiliar Angewandte Chemie. 110: 3579-3582. DOI: 10.1002/(Sici)1521-3757(19981217)110:24<3579::Aid-Ange3579>3.0.Co;2-S |
0.548 |
|
1997 |
Saito S, Kano T, Hatanaka K, Yamamoto H. 2,6-Bis(2-alkylphenyl)-3,5-dimethylphenol as a new chiral phenol with C2-symmetry. Application to the asymmetric alkylation of aldehydes Journal of Organic Chemistry. 62: 5651-5656. DOI: 10.1021/Jo970747G |
0.664 |
|
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