| Year |
Citation |
Score |
| 2023 |
Zhang J, Suzuki K, Ohmori K. Total Syntheses of Sparsomycin and Sparoxomycins A and A via Sulfenate-Anion-Mediated Iterative C-S Bond Formation. Organic Letters. PMID 38090756 DOI: 10.1021/acs.orglett.3c03791 |
0.349 |
|
| 2022 |
Betkekar VV, Suzuki K, Ohmori K. synthesis of dimerization-ready flavan unit intramolecular Pummerer/Friedel-Crafts cascade. Organic & Biomolecular Chemistry. 20: 7419-7423. PMID 36106771 DOI: 10.1039/d2ob01416e |
0.811 |
|
| 2022 |
Betkekar VV, Suzuki K, Ohmori K. Total Synthesis of Parameritannin A2, a Branched Epicatechin Tetramer with Two Double Linkages. Angewandte Chemie (International Ed. in English). PMID 35534438 DOI: 10.1002/anie.202205106 |
0.792 |
|
| 2021 |
Tanaka T, Betkekar VV, Ohmori K, Suzuki K, Shigemori H. Evaluation of Amyloid Polypeptide Aggregation Inhibition and Disaggregation Activity of A-Type Procyanidins. Pharmaceuticals (Basel, Switzerland). 14. PMID 34832900 DOI: 10.3390/ph14111118 |
0.738 |
|
| 2020 |
Takikawa H, Nishii A, Takiguchi H, Yagishita H, Tanaka M, Hirano K, Uchiyama M, Ohmori K, Suzuki K. Intramolecular Benzyne-Phenolate [4+2] Cycloadditions. Angewandte Chemie (International Ed. in English). PMID 32270569 DOI: 10.1002/Anie.202003131 |
0.418 |
|
| 2020 |
Ueda Y, Suzuki K, Ohmori K. Synthesis of Enantiopure -Symmetric Anthracenophane and Dimerization En Route to Multiple-Bridged Cyclophanes. Organic Letters. PMID 32083888 DOI: 10.1021/Acs.Orglett.0C00354 |
0.432 |
|
| 2020 |
Ando Y, Maezawa Y, Shimura J, Kitamura K, Matsumoto T, Suzuki K. Toward Pluramycins with Epoxy Side Chain: Syntheses of Kidamycinone and Epoxykidamycinone (Saptomycinone H). Chemistry, An Asian Journal. PMID 32017465 DOI: 10.1002/Asia.201901807 |
0.563 |
|
| 2020 |
Suzuki K, Ando Y, Asahina H, Kitamura K, Matsumoto T. α-L-Vancosamine Aryl C-Glycosides, Less Stable Anomers: A Problem in Synthesis of Pluramycin-Class Antibiotics Heterocycles. 101: 645. DOI: 10.3987/Com-19-S(F)55 |
0.564 |
|
| 2020 |
Ando Y, Fukazawa T, Ohmori K, Suzuki K. Thiolate-mediated Reductive Cyclizations: Scope, Limitation and Novel Mechanistic Insights Chemistry Letters. 49: 1103-1106. DOI: 10.1246/Cl.200411 |
0.37 |
|
| 2020 |
Takikawa H, Murata K, Sato S, Kawada T, Nakakohara H, Ohmori K, Suzuki K. Synthetic Study on Lactonamycins, Part 2: Stereoselective Access to ABCD-Ring System Synlett. DOI: 10.1055/S-0040-1707198 |
0.388 |
|
| 2019 |
Shimura J, Ando Y, Suzuki K. Hydroxylamine-Mediated Anthrapyranone Formation, Solving 5-exo/6-endo Issue toward Synthesis of Pluramycin-Class Antibiotics. Organic Letters. PMID 31841345 DOI: 10.1021/Acs.Orglett.9B04127 |
0.387 |
|
| 2019 |
Betkekar VV, Harachi M, Suzuki K, Ohmori K. Syntheses of doubly linked proanthocyanidins using free flavan units as nucleophiles: insight into the origin of the high regioselectivity of annulation. Organic & Biomolecular Chemistry. PMID 31584055 DOI: 10.1039/C9Ob01896D |
0.788 |
|
| 2019 |
Ando Y, Tanaka D, Sasaki R, Ohmori K, Suzuki K. Stereochemical Dichotomy in Two Competing Cascade Processes: Total Syntheses of Both Enantiomers of Spiroxin A. Angewandte Chemie (International Ed. in English). PMID 31278822 DOI: 10.1002/Anie.201906762 |
0.391 |
|
| 2019 |
Nishii A, Takikawa H, Suzuki K. 2-Bromo-6-(chlorodiisopropylsilyl)phenyl tosylate as an efficient platform for intramolecular benzyne-diene [4 + 2] cycloaddition. Chemical Science. 10: 3840-3845. PMID 31015926 DOI: 10.1039/C8Sc05518A |
0.344 |
|
| 2019 |
Azami K, Hayashi T, Kusumi T, Ohmori K, Suzuki K. First Total Synthesis of Carthamin, a Traditional Natural Red Pigment. Angewandte Chemie (International Ed. in English). PMID 30802362 DOI: 10.1002/Anie.201900454 |
0.413 |
|
| 2019 |
Ninomiya M, Ando Y, Kudo F, Ohmori K, Suzuki K. First Total Synthesis of Actinorhodin. Angewandte Chemie (International Ed. in English). PMID 30690838 DOI: 10.1002/Anie.201814172 |
0.456 |
|
| 2019 |
Ando Y, Fukazawa T, Hori S, Ohmori K, Suzuki K. Thiolate-mediated reductive cyclization: asymmetric total synthesis of (+)-engelharquinone Phosphorus Sulfur and Silicon and the Related Elements. 194: 723-725. DOI: 10.1080/10426507.2019.1603718 |
0.488 |
|
| 2019 |
Matsuoka S, Nakamura K, Ohmori K, Suzuki K. General Synthetic Approach to Rotenoids via Stereospecific, Group-Selective 1,2-Rearrangement and Dual SNAr Cyclizations of Aryl Fluorides Synthesis. 51: 1139-1156. DOI: 10.1055/S-0037-1611654 |
0.405 |
|
| 2018 |
Maturi MM, Ohmori K, Suzuki K. Synthesis of Oxygenated -Methylbenzaldehydes Aryne [2+2] Cycloaddition and Benzocyclobutenol Ring Opening. Chimia. 72: 870-873. PMID 30648953 DOI: 10.2533/Chimia.2018.870 |
0.434 |
|
| 2018 |
Takikawa H, Nishii A, Sakai T, Suzuki K. Aryne-based strategy in the total synthesis of naturally occurring polycyclic compounds. Chemical Society Reviews. 47: 8030-8056. PMID 30357181 DOI: 10.1039/C8Cs00350E |
0.356 |
|
| 2018 |
Wakita F, Ando Y, Ohmori K, Suzuki K. Model Reactions for the Enantioselective Synthesis of γ-Rubromycin: Stereospecific Intramolecular Photoredox Cyclization of an ortho-Quinone Ether to a Spiroacetal. Organic Letters. PMID 29932661 DOI: 10.1021/Acs.Orglett.8B01475 |
0.471 |
|
| 2018 |
Ando Y, Wakita F, Ohmori K, Suzuki K. Intramolecular photoredox reactions of 1,2-naphthoquinone derivatives. Bioorganic & Medicinal Chemistry Letters. PMID 29880402 DOI: 10.1016/J.Bmcl.2018.05.056 |
0.374 |
|
| 2018 |
Yamada T, Takiguchi H, Ohmori K, Suzuki K. Total Syntheses of Pusilatins A-C, Liverwort-Derived Macrocyclic Bisbibenzyl Dimers. Organic Letters. PMID 29863362 DOI: 10.1021/Acs.Orglett.8B01366 |
0.388 |
|
| 2018 |
Ando Y, Suzuki K. Photoredox Reaction of Quinones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29732621 DOI: 10.1002/Chem.201801064 |
0.389 |
|
| 2018 |
Noguchi Y, Takeda R, Suzuki K, Ohmori K. Total Synthesis of Selligueain A, a Sweet Flavan Trimer. Organic Letters. PMID 29659295 DOI: 10.1021/Acs.Orglett.8B00873 |
0.404 |
|
| 2018 |
Yamashita Y, Hirano Y, Takada A, Takikawa H, Suzuki K. Total Synthesis of Bis-anthraquinone Antibiotic BE-43472B Synthesis. 50: 2490-2515. DOI: 10.1055/S-0037-1610136 |
0.473 |
|
| 2018 |
Ohmori K, Sakai T, Suzuki K. First Total Synthesis of Oxirapentyn D, a Highly Oxidized Chromene Natural Product Synlett. 29: 1351-1357. DOI: 10.1055/S-0036-1591563 |
0.382 |
|
| 2018 |
Ando Y, Suzuki K. Frontispiece: Photoredox Reactions of Quinones Chemistry: a European Journal. 24. DOI: 10.1002/Chem.201886062 |
0.317 |
|
| 2017 |
Kitamura K, Ando Y, Matsumoto T, Suzuki K. Total Synthesis of Aryl C-Glycoside Natural Products: Strategies and Tactics. Chemical Reviews. PMID 29281269 DOI: 10.1021/Acs.Chemrev.7B00380 |
0.613 |
|
| 2017 |
Sato S, Sakata K, Hashimoto Y, Takikawa H, Suzuki K. First Total Syntheses of Tetracenomycins C and X. Angewandte Chemie (International Ed. in English). PMID 28762249 DOI: 10.1002/Anie.201707099 |
0.771 |
|
| 2017 |
Ando Y, Hanaki A, Sasaki R, Ohmori K, Suzuki K. Stereospecificity in Intramolecular Photoredox Reactions of Naphthoquinones: Enantioselective Total Synthesis of (-)-Spiroxin C. Angewandte Chemie (International Ed. in English). PMID 28671750 DOI: 10.1002/Anie.201705562 |
0.483 |
|
| 2017 |
Fukazawa T, Ando Y, Ohmori K, Hayashi T, Suzuki K. Enantioselective Access to Bicyclo[3.2.1]octadienone Skeleton: Total Syntheses of (+)-Engelharquinone and Its Epoxide. Organic Letters. PMID 28248526 DOI: 10.1021/Acs.Orglett.7B00464 |
0.452 |
|
| 2017 |
Hayashi T, Ohmori K, Suzuki K. Synthetic Study on Carthamin. 2. Stereoselective Approach to C-Glycosyl Quinochalcone via Desymmetrization. Organic Letters. PMID 28165754 DOI: 10.1021/Acs.Orglett.6B03899 |
0.372 |
|
| 2017 |
Takikawa H, Sato S, Seki R, Suzuki K. Oxidative Ring Opening of Benzocyclobutenone Oximes: Novel Access to Stable Nitrile Oxides Chemistry Letters. 46: 998-1000. DOI: 10.1246/Cl.170328 |
0.35 |
|
| 2017 |
Sato S, Kawada T, Takikawa H, Suzuki K. Preparation of 2-Substituted 3-Methoxycarbonyl-4-methoxyfurans that Allow Access to Highly Functionalized Naphthalenes via Regioselective Cycloaddition with Alkoxybenzyne Synlett. 28: 1719-1723. DOI: 10.1055/S-0036-1590825 |
0.423 |
|
| 2017 |
Ando Y, Matsumoto T, Suzuki K. Intramolecular Photoredox Reaction of Naphthoquinone Derivatives Synlett. 28: 1040-1045. DOI: 10.1055/S-0036-1590426 |
0.391 |
|
| 2017 |
Suzuki K, Ohmori K, Matsushita K. Total Syntheses of Atrovenetin and Atrovenetinone: A Naphthalene-Annulation Approach to a Discoid Tricycle Using Allenic Acid Synlett. 28: 944-950. DOI: 10.1055/S-0036-1588944 |
0.357 |
|
| 2017 |
Hintermann L, Altmann PJ, Naumov P, Suzuki K. Synthesis of Tetraoxygenated Terephthalates via a Dichloroquinone Route: Characterization of Cross-Conjugated Liebermann
Betaine Intermediates Helvetica Chimica Acta. 100: e1600392. DOI: 10.1002/Hlca.201600392 |
0.353 |
|
| 2016 |
Nakamura K, Ohmori K, Suzuki K. Stereocontrolled Total Syntheses of (-)-Rotenone and (-)-Dalpanol by 1,2-Rearrangement and SN Ar Oxycyclizations. Angewandte Chemie (International Ed. in English). PMID 27910179 DOI: 10.1002/Anie.201609253 |
0.356 |
|
| 2016 |
Ho TC, Kamimura H, Ohmori K, Suzuki K. Total Synthesis of (+)-Vicenin-2. Organic Letters. PMID 27569251 DOI: 10.1021/Acs.Orglett.6B02203 |
0.407 |
|
| 2016 |
Takikawa H, Ishikawa Y, Yoshinaga Y, Hashimoto Y, Kusumi T, Suzuki K. Pleospdione, A Tricyclic Natural Product with Dense Oxygenation at the A-Ring: Total Synthesis and Incongruity of the Originally Assigned Structure and its C3-Epimer Bulletin of the Chemical Society of Japan. 89: 941-954. DOI: 10.1246/Bcsj.20160134 |
0.444 |
|
| 2016 |
Suzuki K, Hirano Y, Tokudome K, Takikawa H. Synthetic Study on Acremoxanthone A: Construction of Bicyclo [3.2.2]nonane CD Skeleton and Fusion of AB Rings Synlett. 28: 214-220. DOI: 10.1055/S-0036-1588600 |
0.38 |
|
| 2016 |
Takikawa H, Nishii A, Suzuki K. Synthesis of β-Hydroxynaphthoate Derivatives from Ketodioxinones via Benzyne Acyl-Alkylation and Aldol Condensation Cascade Synthesis. 48: 3331-3338. DOI: 10.1055/S-0035-1562514 |
0.429 |
|
| 2016 |
Ohmori K, Suzuki K, Hayashi T. Synthetic Study on Carthamin: Problem and Solution for Oxidative Dearomatization Approach to Quinol C-Glycoside Synlett. 27: 2345-2351. DOI: 10.1055/S-0035-1562511 |
0.397 |
|
| 2016 |
Jung S, Kitajima Y, Ueda Y, Suzuki K, Ohmori K. Stereocontrolled Synthesis of Planar Chiral Carba-Paracyclophanes via Modular Assembly Synlett. DOI: 10.1055/S-0035-1561937 |
0.396 |
|
| 2016 |
Jung S, Ueda Y, Suzuki K, Ohmori K. Facile Synthesis of Stereodefined α-Iodovinyl Sulfoxides, Versatile Platform to Trisubstituted Olefins Synlett. 27: 2024-2028. DOI: 10.1055/S-0035-1561654 |
0.424 |
|
| 2016 |
Yamaguchi S, Takahashi N, Yuyama D, Sakamoto K, Suzuki K, Matsumoto T. First Total Synthesis of Dermocanarin 2 Synlett. 27: 1262-1268. DOI: 10.1055/S-0035-1561417 |
0.475 |
|
| 2016 |
Nakayama R, Tanzer E, Kusumi T, Ohmori K, Suzuki K. Total Synthesis of the Proposed Structure of Ardimerin, and Proposal for its Structural Revision Helvetica Chimica Acta. 99: 944-960. DOI: 10.1002/Hlca.201600244 |
0.401 |
|
| 2015 |
Morita M, Ohmori K, Suzuki K. Total Syntheses of Perenniporides. Organic Letters. PMID 26555442 DOI: 10.1021/Acs.Orglett.5B02906 |
0.416 |
|
| 2015 |
Sakata J, Ando Y, Ohmori K, Suzuki K. Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle. Organic Letters. 17: 3746-9. PMID 26225897 DOI: 10.1021/Acs.Orglett.5B01732 |
0.413 |
|
| 2015 |
Ando Y, Hori S, Fukazawa T, Ohmori K, Suzuki K. Toward Naphthocyclinones: Doubly Connected Octaketide Dimers with a Bicyclo[3.2.1]octadienone Core by Thiolate-Mediated Cyclization. Angewandte Chemie (International Ed. in English). 54: 9650-3. PMID 26118656 DOI: 10.1002/Anie.201503442 |
0.433 |
|
| 2015 |
Aoki Y, Ohmori K, Suzuki K. Dioxanone-fused dienes enable highly endo-selective intramolecular Diels-Alder reactions. Organic Letters. 17: 2756-9. PMID 25972124 DOI: 10.1021/Acs.Orglett.5B01172 |
0.409 |
|
| 2015 |
Nakamura K, Ohmori K, Suzuki K. The flavan-isoflavan rearrangement: bioinspired synthetic access to isoflavonoids via 1,2-shift-alkylation sequence. Chemical Communications (Cambridge, England). 51: 7012-4. PMID 25803199 DOI: 10.1039/C5Cc01572C |
0.416 |
|
| 2015 |
Kitamura K, Ando Y, Maezawa Y, Matsumoto T, Suzuki K. Toward the pluramycins: Route exploration from dihydroxyanthrone tricyclic platform to an aglycon, saptomycinone B Heterocycles. 90: 1240-1253. DOI: 10.3987/Com-14-S(K)106 |
0.493 |
|
| 2014 |
Watanabe G, Ohmori K, Suzuki K. A seco-catechin cyclization approach to 4→6-linked catechin dimers. Chemical Communications (Cambridge, England). 50: 14371-3. PMID 25296616 DOI: 10.1039/C4Cc06390B |
0.454 |
|
| 2014 |
Ito Y, Ohmori K, Suzuki K. Annulation approach to doubly linked (A-type) oligocatechins: syntheses of (+)-procyanidin A₂ and (+)-cinnamtannin B₁. Angewandte Chemie (International Ed. in English). 53: 10129-33. PMID 25070773 DOI: 10.1002/Anie.201405600 |
0.393 |
|
| 2014 |
Kitamura K, Ando Y, Matsumoto T, Suzuki K. Synthesis of the pluramycins 1: two designed anthrones as enabling platforms for flexible bis-C-glycosylation. Angewandte Chemie (International Ed. in English). 53: 1258-61. PMID 24375957 DOI: 10.1002/Anie.201308016 |
0.603 |
|
| 2014 |
Kitamura K, Maezawa Y, Ando Y, Kusumi T, Matsumoto T, Suzuki K. Synthesis of the pluramycins 2: total synthesis and structure assignment of saptomycin B. Angewandte Chemie (International Ed. in English). 53: 1262-5. PMID 24356940 DOI: 10.1002/Anie.201308017 |
0.64 |
|
| 2014 |
Takikawa H, Hashimoto Y, Suzuki K. Isoxazole Platform for Polyketide Assembly: Cycloaddition of Stable Benzonitrile Oxides to Stableortho-Quinone Monoacetals and Dehydrogenation Chemistry Letters. 43: 1607-1609. DOI: 10.1246/Cl.140574 |
0.351 |
|
| 2014 |
Tsuji T, Suzuki K, Nakamura T, Nishi T. ChemInform Abstract: Synthesis of a Chiral Phosphonium Salt for the Preparation of α-Substituted Alaninol Derivatives. Cheminform. 45: no-no. DOI: 10.1002/chin.201451056 |
0.338 |
|
| 2013 |
Takiguchi H, Ohmori K, Suzuki K. Synthesis and determination of the absolute configuration of cavicularin by a symmetrization/asymmetrization approach. Angewandte Chemie (International Ed. in English). 52: 10472-6. PMID 23956143 DOI: 10.1002/Anie.201304929 |
0.42 |
|
| 2013 |
Yamashita Y, Hirano Y, Takada A, Takikawa H, Suzuki K. Total synthesis of the antibiotic BE-43472B. Angewandte Chemie (International Ed. in English). 52: 6658-61. PMID 23677772 DOI: 10.1002/Anie.201301591 |
0.344 |
|
| 2013 |
Watanabe G, Ohmori K, Suzuki K. First regiocontrolled synthesis of procyanidin B6, a catechin dimer with rare connectivity: a halo-capping strategy for formation of 4,6-interflavan bonds. Chemical Communications (Cambridge, England). 49: 5210-2. PMID 23625307 DOI: 10.1039/C3Cc41993B |
0.394 |
|
| 2013 |
Kitamura K, Shigeta M, Maezawa Y, Watanabe Y, Hsu DS, Ando Y, Matsumoto T, Suzuki K. Preparation of L-vancosamine-related glycosyl donors. The Journal of Antibiotics. 66: 131-9. PMID 23423169 DOI: 10.1038/Ja.2013.2 |
0.589 |
|
| 2013 |
Fujimoto Y, Itakura R, Hoshi H, Yanai H, Ando Y, Suzuki K, Matsumoto T. Novel one-pot synthesis of xanthones via sequential fluoride ion-promoted fries-type rearrangement and nucleophilic aromatic substitution Synlett. 24: 2575-2580. DOI: 10.1055/S-0033-1339881 |
0.444 |
|
| 2012 |
Yano T, Ohmori K, Takahashi H, Kusumi T, Suzuki K. Unified approach to catechin hetero-oligomers: first total synthesis of trimer EZ-EG-CA isolated from Ziziphus jujuba. Organic & Biomolecular Chemistry. 10: 7685-8. PMID 22930202 DOI: 10.1039/C2Ob26337H |
0.38 |
|
| 2012 |
Stadlbauer S, Ohmori K, Hattori F, Suzuki K. A new synthetic strategy for catechin-class polyphenols: concise synthesis of (-)-epicatechin and its 3-O-gallate. Chemical Communications (Cambridge, England). 48: 8425-7. PMID 22790234 DOI: 10.1039/C2Cc33704E |
0.388 |
|
| 2012 |
Hashimoto Y, Takada A, Takikawa H, Suzuki K. Synthesis of isoxazoles en route to semi-aromatized polyketides: dehydrogenation of benzonitrile oxide–para-quinone acetal cycloadducts Organic and Biomolecular Chemistry. 10: 6003-6009. PMID 22595976 DOI: 10.1039/C2Ob25423A |
0.798 |
|
| 2012 |
Hamura T, Chuda Y, Nakatsuji Y, Suzuki K. Catalytic Generation of Arynes and Trapping by Nucleophilic Addition and Iodination Angewandte Chemie. 51: 3368-3372. PMID 22359268 DOI: 10.1002/Anie.201108415 |
0.341 |
|
| 2012 |
Fukui N, Ohmori K, Suzuki K. Synthesis and structure revision of goupiolone A: A benzotropolone natural product Helvetica Chimica Acta. 95: 2194-2217. DOI: 10.1002/Hlca.201200439 |
0.404 |
|
| 2011 |
Hamura T, Iwata S, Suzuki K. A domino pericyclic route to polysubstituted salicylic acid derivatives: four sequential processes from enynones and ketene silyl acetals Chemical Communications. 47: 6891-6893. PMID 21594302 DOI: 10.1039/C1Cc11758K |
0.394 |
|
| 2011 |
Takahashi N, Kanayama T, Okuyama K, Kataoka H, Fukaya H, Suzuki K, Matsumoto T. Enantioselective total synthesis of (-)-euxanmodin B: an axially chiral natural product with an anthraquinone-xanthone composite structure. Chemistry, An Asian Journal. 6: 1752-6. PMID 21557490 DOI: 10.1002/Asia.201100187 |
0.379 |
|
| 2011 |
Takada A, Hashimoto Y, Takikawa H, Hikita K, Suzuki K. Total Synthesis and Absolute Stereochemistry of Seragakinone A Angewandte Chemie. 50: 2297-2301. PMID 21351340 DOI: 10.1002/Anie.201006528 |
0.794 |
|
| 2011 |
Koyama Y, Kataoka H, Suzuki K, Matsumoto T. Regioselective remote functionalization of biaryl framework via tethered ortho-quinol intermediate. Chemistry-An Asian Journal. 6: 355-358. PMID 20872398 DOI: 10.1002/Asia.201000533 |
0.332 |
|
| 2011 |
Seo H, Ohmori K, Suzuki K. Regioselective Approach to Multisubstituted Benzenes Chemistry Letters. 40: 744-746. DOI: 10.1246/Cl.2011.744 |
0.375 |
|
| 2011 |
Hayashi T, Ohmori K, Suzuki K. Ring Expansion Approach to Azaspiro[4.5]decane Skeletons via Electrophilic Activation of Benzocyclobutenols Bearing Pyridyl Group Chemistry Letters. 40: 612-613. DOI: 10.1246/Cl.2011.612 |
0.342 |
|
| 2011 |
Fukui N, Hamura T, Ohmori K, Suzuki K. Ring Expansion of Cyclopropylbenzocyclobutenes En Route to Benzocycloheptenes Chemistry Letters. 40: 1198-1200. DOI: 10.1246/Cl.2011.1198 |
0.347 |
|
| 2011 |
Aoki Y, Mochizuki Y, Yoshinari T, Ohmori K, Suzuki K. Expeditious Modular Assembly of Multisubstituted Cyclohexanes via Dioxanone–Dienes Chemistry Letters. 40: 1192-1194. DOI: 10.1246/Cl.2011.1192 |
0.347 |
|
| 2011 |
Takiguchi H, Ohmori K, Suzuki K. Concise Synthesis of Riccardin C, Macrocyclic Bisbibenzyl Natural Product Chemistry Letters. 40: 1069-1071. DOI: 10.1246/Cl.2011.1069 |
0.479 |
|
| 2011 |
Takada A, Hashimoto Y, Takikawa H, Hikita K, Suzuki K. Synthesis of ent-SeragakinoneA Synfacts. 2011: 581-581. DOI: 10.1055/S-0030-1260367 |
0.453 |
|
| 2011 |
Ben A, Hsu D, Matsumoto T, Suzuki K. Total synthesis and structure revision of deacetylravidomycin M Tetrahedron. 67: 6460-6468. DOI: 10.1016/J.Tet.2011.06.046 |
0.482 |
|
| 2010 |
Suzuki K. Lessons from total synthesis of hybrid natural products Chemical Record. 10: 291-307. PMID 20878641 DOI: 10.1002/Tcr.201000030 |
0.365 |
|
| 2010 |
Iwata S, Hamura T, Suzuki K. Siloxy(trialkoxy)ethene undergoes regioselective [2+2] cycloaddition to ynones and ynoates en route to functionalized cyclobutenediones Chemical Communications. 46: 5316-5318. PMID 20556302 DOI: 10.1039/C0Cc00883D |
0.387 |
|
| 2010 |
Ohmori K, Yano T, Suzuki K. General synthesis of epi-series catechins and their 3-gallates: reverse polarity strategy. Organic and Biomolecular Chemistry. 8: 2693-2696. PMID 20386808 DOI: 10.1039/C003464A |
0.401 |
|
| 2010 |
Shinozaki S, Hamura T, Ibusuki Y, Fujii K, Uekusa H, Suzuki K. Hexaradialenes by successive ring openings of tris(alkoxy-tricyclobutabenzenes): synthesis and characterization. Angewandte Chemie (International Ed. in English). 49: 3026-9. PMID 20333636 DOI: 10.1002/Anie.200907305 |
0.42 |
|
| 2010 |
Yoshinari T, Ohmori K, Schrems MG, Pfaltz A, Suzuki K. Total synthesis and absolute configuration of macrocidin A, a cyclophane tetramic acid natural product Angewandte Chemie - International Edition. 49: 881-885. PMID 20039248 DOI: 10.1002/Anie.200906362 |
0.372 |
|
| 2010 |
Yoshinari T, Ohmori K, Suzuki K. anti-Selective Vinylogous Aldol Reaction by Silylated Alkyldioxinone Dienolate Chemistry Letters. 39: 1042-1044. DOI: 10.1246/Cl.2010.1042 |
0.344 |
|
| 2010 |
Suzuki K, Matsumoto T, Shigeta M, Hakamata T, Watanabe Y, Kitamura K, Ando Y. Efficient Bis-C-Aminoglycosylation toward the Synthesis of the Pluramycins Synlett. 2010: 2654-2658. DOI: 10.1055/S-0030-1258766 |
0.607 |
|
| 2010 |
Yoshinari T, Ohmori K, Schrems MG, Pfaltz A, Suzuki K. Synthesis of (+)-Macrocidin A Synfacts. 2010: 627-627. DOI: 10.1055/S-0029-1219852 |
0.453 |
|
| 2010 |
Mori K, Ohmori K, Suzuki K. Synthesis of Antibiotic TAN-1085 Synfacts. 2010: 4-4. DOI: 10.1055/S-0029-1218401 |
0.392 |
|
| 2010 |
Abe M, Ohmori K, Suzuki K, Yamamoto T. Synthesis and chiroptical properties of π-conjugated polymer consisting of dihydropentahelicene units with axial chirality Journal of Polymer Science Part a: Polymer Chemistry. 48: 1844-1848. DOI: 10.1002/Pola.23944 |
0.333 |
|
| 2010 |
Matsumoto T, Konegawa T, Nakamura T, Suzuki K. ChemInform Abstract: Facile and Highly Enantioselective Synthesis of Axially Chiral Biaryls by Enzymatic Desymmetrization. Cheminform. 33: no-no. DOI: 10.1002/chin.200219097 |
0.341 |
|
| 2010 |
Yamanoi S, Matsumoto T, Suzuki K. ChemInform Abstract: Regioselectivity of MAO-Catalyzed Allylmetalation of Conjugated Enynes with Allylzirconiums. Cheminform. 30: no-no. DOI: 10.1002/chin.199910071 |
0.321 |
|
| 2010 |
SUZUKI K, MATSUMOTO T. ChemInform Abstract: Synthesis of Glycosylarenes Cheminform. 28: no-no. DOI: 10.1002/chin.199732233 |
0.34 |
|
| 2010 |
SUZUKI K, MATSUMOTO T, HOSOYA T. ChemInform Abstract: Total Synthesis of the Gilvocarcins Cheminform. 27: no-no. DOI: 10.1002/chin.199621272 |
0.335 |
|
| 2010 |
NAGASAWA T, ONOGUCHI Y, MATSUMOTO T, SUZUKI K. ChemInform Abstract: Short-Step Total Synthesis of a Cyclopropane-Containing Eicosanoid. Cheminform. 27: no-no. DOI: 10.1002/chin.199611293 |
0.335 |
|
| 2010 |
MATSUMOTO T, SOHMA T, YAMAGUCHI H, KURATA S, SUZUKI K. ChemInform Abstract: Total Synthesis of Antibiotic C104: Benzyne-Furan Cycloaddition Approach to the Angucyclines. Cheminform. 26: no-no. DOI: 10.1002/chin.199543271 |
0.304 |
|
| 2010 |
MATSUMOTO T, SOHMA T, YAMAGUCHI H, KURATA S, SUZUKI K. ChemInform Abstract: Benzyne-Furan Cycloaddition Approach to the Angucyclines: First Total Synthesis of Antibiotic C104. Cheminform. 26: no-no. DOI: 10.1002/chin.199532239 |
0.304 |
|
| 2010 |
SHIMAZAKI M, MORIMOTO M, SUZUKI K. ChemInform Abstract: Stereoselective Construction of Three- and Four-Contiguous Asymmetric Centers: Novel Possibility by Alkylative Rearrangement of Epoxy Silyl Ethers. Cheminform. 22: no-no. DOI: 10.1002/chin.199128068 |
0.342 |
|
| 2009 |
Komiya T, Goto N, Takeda A, Horike K, Onoda H, Sakai K, Kitamura K, Yamamoto K, Oikawa T, Nagasaka T, Hiramitsu T, Simabukuro S, Suzuki K, Sato T, Yoshihiko W, et al. A case of acute rejection with adenovirus infection after ABO-incompatible kidney transplantation. Clinical Transplantation. 23: 27-30. PMID 19594592 DOI: 10.1111/j.1399-0012.2009.01005.x |
0.383 |
|
| 2009 |
Mori K, Ohmori K, Suzuki K. Stereochemical Relay via Axially Chiral Styrenes: Asymmetric Synthesis of the Antibiotic TAN‐1085 Angewandte Chemie. 48: 5633-5637. PMID 19569154 DOI: 10.1002/Anie.200901968 |
0.413 |
|
| 2009 |
Mori K, Ohmori K, Suzuki K. Hydrogen‐Bond Control in Axially Chiral Styrenes: Selective Synthesis of Enantiomerically Pure C2‐Symmetric Paracyclophanes Angewandte Chemie. 48: 5638-5641. PMID 19562815 DOI: 10.1002/Anie.200901974 |
0.385 |
|
| 2009 |
Masuo R, Ohmori K, Hintermann L, Yoshida S, Suzuki K. First stereoselective total synthesis of FD-594 aglycon. Angewandte Chemie (International Ed. in English). 48: 3462-5. PMID 19347912 DOI: 10.1002/Anie.200806338 |
0.473 |
|
| 2009 |
Ohmori K, Takeda M, Higuchi T, Shono T, Suzuki K. Stereocontolled Synthesis of (−)-Afzelechin: General Route to Catechin-class Polyphenols by Solving an SN2 vs. SN1 Problem Chemistry Letters. 38: 934-935. DOI: 10.1246/Cl.2009.934 |
0.388 |
|
| 2009 |
Masuo R, Ohmori K, Hintermann L, Yoshida S, Suzuki K. Synthesis of FD-594 Aglycon Synfacts. 2009: 1064-1064. DOI: 10.1055/S-0029-1217860 |
0.454 |
|
| 2009 |
Onoda T, Takikawa Y, Fujimoto T, Yasui Y, Suzuki K, Matsumoto T. Synthesis of (+)-11-Hydroxyerythratidine Synfacts. 2009: 948-948. DOI: 10.1055/S-0029-1217608 |
0.453 |
|
| 2009 |
Matsumoto T, Okuyama K, Shingubara K, Tsujiyama S, Suzuki K. Enantiodivergent Synthesis of Tetra-ortho-Substituted Biphenyls by Enzymatic Desymmetrization Synlett. 2009: 941-944. DOI: 10.1055/S-0028-1088215 |
0.424 |
|
| 2009 |
Matsumoto T, Onoda T, Takikawa Y, Fujimoto T, Yasui Y, Suzuki K. First Total Synthesis of (+)-11-Hydroxyerythratidine Synlett. 2009: 1041-1046. DOI: 10.1055/S-0028-1088157 |
0.49 |
|
| 2008 |
Hintermann L, Masuo R, Suzuki K. Solvent-controlled leaving-group selectivity in aromatic nucleophilic substitution. Organic Letters. 10: 4859-62. PMID 18841994 DOI: 10.1021/Ol801962A |
0.373 |
|
| 2008 |
Takikawa H, Takada A, Hikita K, Suzuki K. Formation of α-Hydroxy-β-diketones through Hydroxylation of Isoxazolium Salts: Stereoselective Approach to Angular cis-Diols in Polycyclic Systems† Angewandte Chemie. 47: 7446-7449. PMID 18712721 DOI: 10.1002/Anie.200801586 |
0.31 |
|
| 2008 |
Suzuki T, Hamura T, Suzuki K. Ring Selectivity: Successive Ring Expansion of Two Benzocyclobutenes for Divergent Access to Angular and Linear Benzanthraquinones Angewandte Chemie. 47: 2248-2252. PMID 18275059 DOI: 10.1002/Anie.200705630 |
0.304 |
|
| 2008 |
Koyama Y, Yamaguchi R, Suzuki K. Total synthesis and structure assignment of the anthrone C-glycoside cassialoin. Angewandte Chemie. 47: 1084-1087. PMID 18163372 DOI: 10.1002/Anie.200704625 |
0.384 |
|
| 2008 |
Mori K, Tanaka Y, Ohmori K, Suzuki K. Synthesis and Stereochemical Assignment of Angucycline Antibiotic, PD-116740 Chemistry Letters. 37: 470-471. DOI: 10.1246/Cl.2008.470 |
0.341 |
|
| 2008 |
Arisawa T, Hamura T, Uekusa H, Matsumoto T, Suzuki K. Linearly Fused Dicyclobutabenzenes via Dual, Regioselective Cycloadditions of 1,4-Benzdiyne Equivalent and Ketene Silyl Acetals Synlett. 2008: 1179-1184. DOI: 10.1055/S-2008-1072729 |
0.436 |
|
| 2008 |
Hintermann L, Suzuki K. 2,5-Dihydroxyterephthalates, 2,5-Dichloro-1,4-benzoquinone-3,6-dicarboxylates,and Polymorphic 2,5-Dichloro-3,6-dihydroxyterephthalates Synthesis. 2008: 2303-2306. DOI: 10.1055/S-2008-1067145 |
0.3 |
|
| 2007 |
Tamiya M, Ohmori K, Kitamura M, Kato H, Arai T, Oorui M, Suzuki K. General Synthesis Route to Benanomicin‐Pradimicin Antibiotics Chemistry: a European Journal. 13: 9791-9823. PMID 17907132 DOI: 10.1002/Chem.200700863 |
0.471 |
|
| 2007 |
Takikawa H, Suzuki K. Modified chiral triazolium salts for enantioselective benzoin cyclization of enolizable keto-aldehydes: synthesis of (+)-sappanone B. Organic Letters. 9: 2713-6. PMID 17559218 DOI: 10.1021/Ol070929P |
0.421 |
|
| 2007 |
Suzuki K, Takikawa H, Hachisu Y, Bode JW. Isoxazole-directed pinacol rearrangement: Stereocontrolled approach to angular stereogenic centers Angewandte Chemie - International Edition. 46: 3252-3254. PMID 17385784 DOI: 10.1002/Anie.200605138 |
0.516 |
|
| 2007 |
Hamura T, Arisawa T, Matsumoto T, Suzuki K. Two-directional annelation: dual benzyne cycloadditions starting from bis(sulfonyloxy)diiodobenzene. Angewandte Chemie (International Ed. in English). 45: 6842-4. PMID 16991163 DOI: 10.1002/Anie.200602539 |
0.366 |
|
| 2007 |
Hamura T, Suzuki T, Matsumoto T, Suzuki K. Tandem ring expansion of alkenyl benzocyclobutenol derivatives into substituted naphthols. Angewandte Chemie (International Ed. in English). 45: 6294-6. PMID 16937419 DOI: 10.1002/Anie.200602428 |
0.374 |
|
| 2007 |
Suzuki K. Studies on Organic Synthesis Inspired by Carbohydrates Cheminform. 38. DOI: 10.5059/Yukigoseikyokaishi.65.175 |
0.445 |
|
| 2007 |
Iwata S, Hamura T, Matsumoto T, Suzuki K. Mukaiyama Aldol Reaction of Ester Acceptors: Organoaluminums Catalyze Nucleophilic Addition of Ketene Silyl Acetals Chemistry Letters. 36: 538-539. DOI: 10.1246/Cl.2007.538 |
0.455 |
|
| 2007 |
Ohmori K, Furuya S, Yamanoi S, Suzuki K. Two Isolable Conformers of Dihydropentahelicenediol Derivatives: Stereochemical Property and Its Utility for Asymmetric Reactions Chemistry Letters. 36: 328-329. DOI: 10.1246/Cl.2007.328 |
0.381 |
|
| 2007 |
Takikawa H, Hikita K, Suzuki K. Synthesis of Highly Functionalized Isoxazoles via Base-Promoted Cyclocondensation of Stable Nitrile Oxides with Active Methylene Compounds Synlett. 2007: 2252-2256. DOI: 10.1055/S-2007-985561 |
0.35 |
|
| 2007 |
Suzuki K, Tamiya M, Jäger C, Ohmori K. Stereoselective Access to Functionalized Dihydrophenanthrenes via Reductive Cyclization of Biaryl Ene-Aldehydes Synlett. 2007: 0780-0784. DOI: 10.1055/S-2007-970771 |
0.433 |
|
| 2007 |
Yamauchi T, Watanabe Y, Suzuki K, Matsumoto T. Facile One-Pot Synthesis of Resorcinol Bis-C-Glycosides Possessing Two Identical Sugar Moieties. Cheminform. 38. DOI: 10.1055/S-2006-942526 |
0.437 |
|
| 2007 |
Hsu D, Matsumoto T, Suzuki K. Concise Synthesis of (.+-.)-γ-Indomycinone. Cheminform. 38. DOI: 10.1002/chin.200706197 |
0.32 |
|
| 2006 |
Hamura T, Ibusuki Y, Uekusa H, Matsumoto T, Siegel JS, Baldridge KK, Suzuki K. Dodecamethoxy- and hexaoxotricyclobutabenzene: synthesis and characterization. Journal of the American Chemical Society. 128: 10032-3. PMID 16881630 DOI: 10.1021/Ja064063E |
0.429 |
|
| 2006 |
Takikawa H, Hachisu Y, Bode JW, Suzuki K. Catalytic enantioselective crossed aldehyde-ketone benzoin cyclization. Angewandte Chemie (International Ed. in English). 45: 3492-4. PMID 16637094 DOI: 10.1002/Anie.200600268 |
0.585 |
|
| 2006 |
Hamura T, Ibusuki Y, Uekusa H, Matsumoto T, Suzuki K. Poly-oxygenated tricyclobutabenzenes via repeated [2 + 2] cycloaddition of benzyne and ketene silyl acetal. Journal of the American Chemical Society. 128: 3534-5. PMID 16536523 DOI: 10.1021/Ja0602647 |
0.396 |
|
| 2006 |
Hamura T, Kawano N, Matsumoto T, Suzuki K. Peri-selectivity in Thermolysis of Acyloxybenzocyclobutenes Possessing α,β-Unsaturated Carbonyl Group: Synthesis of 2-Benzoxocin Derivatives Chemistry Letters. 35: 730-731. DOI: 10.1246/Cl.2006.730 |
0.4 |
|
| 2006 |
Hsu D, Matsumoto T, Suzuki K. Concise Synthesis of (±)-γ-Indomycinone Chemistry Letters. 35: 1016-1017. DOI: 10.1246/Cl.2006.1016 |
0.361 |
|
| 2006 |
Higuchi T, Ohmori K, Suzuki K. General and Convenient Approach to Flavan-3-ols: Stereoselective Synthesis of (−)-Gallocatechin Chemistry Letters. 35: 1006-1007. DOI: 10.1246/Cl.2006.1006 |
0.442 |
|
| 2006 |
Suzuki K, Takikawa H, Hachisu Y, Bode J. Asymmetric Intramolecular Crossed Aldehyde-Ketone Benzoin Cyclization Synfacts. 2006: 0725-0725. DOI: 10.1055/S-2006-941910 |
0.595 |
|
| 2006 |
Suzuki K, Matsumoto T, Yamauchi T, Watanabe Y. Bis-C-Glycosylation of Resorcinol Derivatives by an O→C-Glycoside Rearrangement Synlett. 2006: 0399-0402. DOI: 10.1055/S-2006-932463 |
0.403 |
|
| 2006 |
Suzuki K, Hsu D, Matsumoto T. Synthesis of l-Vancosamine Derivatives from Methyl α-d-Mannopyranoside Synlett. 2006: 0469-0471. DOI: 10.1055/S-2006-926231 |
0.417 |
|
| 2006 |
Takemura I, Matsumoto T, Suzuki K. Impressive changeover of reaction course in ring expansion of styrylbenzocyclobutenol under alkoxide-forming conditions Tetrahedron Letters. 47: 6677-6679. DOI: 10.1016/J.Tetlet.2006.06.079 |
0.377 |
|
| 2006 |
Takemura I, Imura K, Matsumoto T, Suzuki K. Convergence in [2+2+2] synthesis of β-phenylnaphthalene motif in polyaromatic natural products Tetrahedron Letters. 47: 6673-6676. DOI: 10.1016/J.Tetlet.2006.06.078 |
0.341 |
|
| 2005 |
Ohmori K, Tamiya M, Kitamura M, Kato H, Oorui M, Suzuki K. Regio‐ and Stereocontrolled Total Synthesis of Benanomicin B Angewandte Chemie. 44: 3871-3874. PMID 15900522 DOI: 10.1002/Anie.200501210 |
0.356 |
|
| 2005 |
Suzuki K, Matsumoto T, Yamauchi T, Shigeta M. Sc(OTf)3-catalyzed C-glycosylation of β-diketones. A facile access to useful precursors of heteroaromatic C-glycosides Heterocycles. 66: 153-160. DOI: 10.3987/Com-05-S(K)65 |
0.354 |
|
| 2005 |
Hatakeyama K, Ohmori K, Suzuki K. Synthesis of (′)-lotthanongine, a novel natural product with a flavan-indole hybrid structure Synlett. 2005: 1311-1315. DOI: 10.1055/S-2005-868485 |
0.418 |
|
| 2005 |
Hsu D, Matsumoto T, Suzuki K. Efficient Synthetic Route to Ravidosamine Derivatives. Cheminform. 36. DOI: 10.1055/S-2005-864792 |
0.467 |
|
| 2004 |
Takemura I, Imura K, Matsumoto T, Suzuki K. Concise three-component synthesis of defucogilvocarcin M. Organic Letters. 6: 2503-2505. PMID 15255676 DOI: 10.1021/Ol049261U |
0.333 |
|
| 2004 |
Ohmori K, Mori K, Ishikawa Y, Tsuruta H, Kuwahara S, Harada N, Suzuki K. Concise Total Synthesis and Structure Assignment of TAN‐1085 Angewandte Chemie. 43: 3167-3171. PMID 15199568 DOI: 10.1002/Anie.200453801 |
0.381 |
|
| 2004 |
Ohmori K, Ushimaru N, Suzuki K. Oligomeric catechins: an enabling synthetic strategy by orthogonal activation and C(8) protection. Proceedings of the National Academy of Sciences of the United States of America. 101: 12002-12007. PMID 15141082 DOI: 10.1073/Pnas.0401651101 |
0.382 |
|
| 2004 |
Hamura T, Ibusuki Y, Sato K, Matsumoto T, Osamura Y, Suzuki K. Strain-induced regioselectivities in reactions of benzyne possessing a fused four-membered ring. Organic Letters. 5: 3551-4. PMID 14507170 DOI: 10.1021/Ol034877P |
0.359 |
|
| 2004 |
Yasui Y, Suzuki K, Matsumoto T. Transmission of Axial Chirality to Spiro Center Chirality, Enabling Enantiospecific Access to Erythrinan Alkaloids. Cheminform. 35. DOI: 10.1055/S-2004-817754 |
0.398 |
|
| 2004 |
Yasui Y, Koga Y, Suzuki K, Matsumoto T. A Novel Approach to Erythrinan Alkaloids by Utilizing Substituted Biphenyl as Building Block Synlett. 2004: 615-618. DOI: 10.1055/S-2004-817753 |
0.436 |
|
| 2004 |
Ben A, Yamauchi T, Matsumoto T, Suzuki K. Sc(OTf)3 as Efficient Catalyst for Aryl C-Glycoside Synthesis. Cheminform. 35. DOI: 10.1055/S-2003-44988 |
0.391 |
|
| 2004 |
Ohmori K, Hatakeyama K, Ohrui H, Suzuki K. Cationic Zirconocene- or Hafnocene-Based Lewis Acids in Organic Synthesis: Glycoside—Flavonoid Analogy. Cheminform. 35. DOI: 10.1016/J.Tet.2003.08.076 |
0.389 |
|
| 2004 |
Hachisu Y, Bode JW, Suzuki K. Thiazolium ylide-catalyzed intramolecular aldehyde-ketone benzoin-forming reactions: Substrate scope Advanced Synthesis and Catalysis. 346: 1097-1100. DOI: 10.1002/Adsc.200404092 |
0.6 |
|
| 2003 |
Hachisu Y, Bode JW, Suzuki K. Catalytic intramolecular crossed aldehyde--ketone benzoin reactions: a novel synthesis of functionalized preanthraquinones. Journal of the American Chemical Society. 125: 8432-3. PMID 12848538 DOI: 10.1021/Ja035308F |
0.633 |
|
| 2003 |
Bode JW, Uesuka H, Suzuki K. Isoxazole --> benzisoxazole rearrangement promoted cascade reactions affording stereodefined polycycles. Organic Letters. 5: 395-8. PMID 12583727 DOI: 10.1021/Ol0272848 |
0.595 |
|
| 2003 |
Bode JW, Hachisu Y, Matsuura T, Suzuki K. Facile construction and divergent transformation of polycyclic isoxazoles: direct access to polyketide architectures. Organic Letters. 5: 391-4. PMID 12583726 DOI: 10.1021/Ol027283F |
0.63 |
|
| 2003 |
Matsuura T, Bode JW, Hachisu Y, Suzuki K. Molecular sieve (MS 4A) promoted cyclocondensation of hindered, aromatic nitrile oxides and cyclic diketones under mild conditions Synlett. 1746-1748. DOI: 10.1055/S-2003-41436 |
0.495 |
|
| 2003 |
Bode JW, Suzuki K. Corrigendum to: “Structural incongruities of coleophomone natural products: insights by total synthesis of a semi-synthetic derivative” Tetrahedron Letters. 44: 5557. DOI: 10.1016/S0040-4039(03)01283-8 |
0.586 |
|
| 2003 |
Bode JW, Suzuki K. Structural incongruities of coleophomone natural products: Insights by total synthesis of a semi-synthetic derivative Tetrahedron Letters. 44: 3559-3563. DOI: 10.1016/S0040-4039(03)00615-4 |
0.56 |
|
| 2003 |
Bode JW, Hachisu Y, Matsuura T, Suzuki K. Amine-promoted cyclocondensation of highly substituted aromatic nitrile oxides with diketones Tetrahedron Letters. 44: 3555-3558. DOI: 10.1016/S0040-4039(03)00614-2 |
0.608 |
|
| 2003 |
Hamura T, Morita M, Matsumoto T, Suzuki K. Synthesis of functionalized biaryl compounds via ring expansion of alkenylcyclobutenones Tetrahedron Letters. 44: 167-170. DOI: 10.1016/S0040-4039(02)02473-5 |
0.364 |
|
| 2003 |
Ohmori K, Ushimaru N, Suzuki K. Stereoselective Substitution of Flavan Skeletons: Synthesis of Dryopteric Acid. Cheminform. 34. DOI: 10.1016/S0040-4039(02)01826-9 |
0.406 |
|
| 2002 |
Suzuki K, Nakata T. Stereoselective convergent synthesis of a trans-fused polycyclic ether ring system including a 4-hydroxy-5-methyl-tetrahydropyran ring Organic Letters. 4: 2739-2741. PMID 12153223 DOI: 10.1021/ol026261q |
0.366 |
|
| 2002 |
Hamura T, Miyamoto M, Matsumoto T, Suzuki K. Synthesis of hindered 1-arylnaphthalene derivatives via ring expansion of benzocyclobutenones. Organic Letters. 4: 229-32. PMID 11796057 DOI: 10.1021/Ol016956B |
0.422 |
|
| 2002 |
Hamura T, Tsuji S, Matsumoto T, Suzuki K. Single Step Synthesis of Cyclooctadienone Derivatives by Reaction of Cyclobutenones with Dienyllithium Chemistry Letters. 31: 750-751. DOI: 10.1246/Cl.2002.750 |
0.433 |
|
| 2002 |
Hamura T, Kakinuma M, Tsuji S, Matsumoto T, Suzuki K. Synthesis of Functionalized Cyclobutene Derivatives via Selective SN2’ Reaction of Dichlorocyclobutenes Chemistry Letters. 31: 748-749. DOI: 10.1246/Cl.2002.748 |
0.438 |
|
| 2002 |
Hamura T, Tsuji S, Matsumoto T, Suzuki K. Synthesis of Benzocyclooctene Derivatives via Thermal Ring Expansion of Dienylbenzocyclobutenes Chemistry Letters. 31: 280-281. DOI: 10.1246/Cl.2002.280 |
0.361 |
|
| 2002 |
Hamura T, Kawano N, Tsuji S, Matsumoto T, Suzuki K. Single-Step Synthesis of Cyclooctadienone Derivatives by Reaction of Alkenylcyclobutenones with Alkenyllithiums: Enhanced Reactivity of 8π Cyclization by Acetylating the Intermediary Lithium Tetraenolate Chemistry Letters. 2002: 1042-1043. DOI: 10.1246/Cl.2002.1042 |
0.446 |
|
| 2002 |
Matsumoto T, Konegawa T, Nakamura T, Suzuki K. Facile and Highly Enantioselective Synthesis of Axially Chiral Biaryls by Enzymatic Desymmetrization Synlett. 2002: 122-124. DOI: 10.1055/S-2002-19349 |
0.43 |
|
| 2002 |
Shinohara T, Suzuki K. Pinacol rearrangement for constructing asymmetric centers adjacent to heterocycles Tetrahedron Letters. 43: 6937-6940. DOI: 10.1016/S0040-4039(02)01626-X |
0.391 |
|
| 2002 |
Ohmori K, Kitamura M, Ishikawa Y, Kato H, Oorui M, Suzuki K. Semi-pinacol strategy for constructing b-ring of pradimicin-benanomicin antibiotics Tetrahedron Letters. 43: 7023-7026. DOI: 10.1016/S0040-4039(02)01608-8 |
0.457 |
|
| 2002 |
Hamura T, Hosoya T, Yamaguchi H, Kuriyama Y, Tanabe M, Miyamoto M, Yasui Y, Matsumoto T, Suzuki K. Facile Access to Versatile Polyaromatic Building Blocks: Selectively Protected Benzocyclobutenedione Derivatives via Regioselective [2+2] Cycloaddition of -Alkoxybenzyne and Ketene Silyl Acetal Helvetica Chimica Acta. 85: 3589-3604. DOI: 10.1002/1522-2675(200211)85:11<3589::Aid-Hlca3589>3.0.Co;2-Z |
0.41 |
|
| 2001 |
Suzuki T, Ohmori K, Suzuki K. Pseudo-C(3)-symmetric tertiary alcohol building block via group-selective hydroalumination: a synthesis of (-)-malyngolide. Organic Letters. 3: 1741-1744. PMID 11405700 DOI: 10.1021/Ol015943V |
0.38 |
|
| 2001 |
Ohmori K, Suzuki T, Taya K, Tanabe D, Ohta T, Suzuki K. Group-selective hydroalumination: a novel route to stereogenic tert-alcohol centers. Organic Letters. 3: 1057-1060. PMID 11277794 DOI: 10.1021/Ol0156704 |
0.336 |
|
| 2001 |
Matsumoto T, Konegawa T, Yamaguchi H, Nakamura T, Sugai T, Suzuki K. Lipase-Catalyzed Asymmetrization of Diacetate of Meso-2-(2-Propynyl)cyclohexane-1,2,3-triol toward the Total Synthesis of Aquayamycin Synlett. 2001: 1650-1652. DOI: 10.1055/S-2001-17487 |
0.492 |
|
| 2001 |
Yamanoi S, Seki K, Matsumoto T, Suzuki K. Regioselective alkylzirconation of internal alkynes Journal of Organometallic Chemistry. 624: 143-150. DOI: 10.1016/S0022-328X(00)00912-8 |
0.418 |
|
| 2000 |
Suzuki K. Synthetic study of ravidomycin, a hybrid natural product Pure and Applied Chemistry. 72: 1783-1786. DOI: 10.1351/Pac200072091783 |
0.423 |
|
| 2000 |
Hosoya T, Hamura T, Kuriyama Y, Miyamoto M, Matsumoto T, Suzuki K. Silicon-Directed Regioselective [2+2] Cycloaddition of α-Alkoxybenzyne and Ketene Silyl Acetals Synlett. 2000: 520-522. DOI: 10.1055/S-2000-6581 |
0.32 |
|
| 2000 |
Futagami S, Ohashi Y, Imura K, Hosoya T, Ohmori K, Matsumoto T, Suzuki K. Total synthesis of ravidomycin: revision of absolute and relative stereochemistry Tetrahedron Letters. 41: 1063-1067. DOI: 10.1016/S0040-4039(99)02235-2 |
0.453 |
|
| 2000 |
Matsumoto T, Yamaguchi H, Tanabe M, Yasui Y, Suzuki K. Synthetic study of aquayamycin. Part 3: First total synthesis Tetrahedron Letters. 41: 8393-8396. DOI: 10.1016/S0040-4039(00)01480-5 |
0.474 |
|
| 2000 |
Yamaguchi H, Konegawa T, Tanabe M, Nakamura T, Matsumoto T, Suzuki K. Synthetic study of aquayamycin. Part 2: Synthesis of the AB ring fragment Tetrahedron Letters. 41: 8389-8392. DOI: 10.1016/S0040-4039(00)01479-9 |
0.448 |
|
| 2000 |
Matsumoto T, Yamaguchi H, Hamura T, Tanabe M, Kuriyama Y, Suzuki K. Synthetic study of aquayamycin. Part 1: Synthesis of 3-(phenylsulfonyl)phthalides possessing a β-C-olivoside Tetrahedron Letters. 41: 8383-8387. DOI: 10.1016/S0040-4039(00)01478-7 |
0.432 |
|
| 2000 |
Kato H, Ohmori K, Suzuki K. Glycosylation study on pradimicin–benanomicin antibiotics Tetrahedron Letters. 41: 6827-6832. DOI: 10.1016/S0040-4039(00)01153-9 |
0.323 |
|
| 2000 |
Ohmori K, Ohrui H, Suzuki K. First synthesis of astilbin, biologically active glycosyl flavonoid isolated from Chinese folk medicine Tetrahedron Letters. 41: 5537-5541. DOI: 10.1016/S0040-4039(00)00826-1 |
0.391 |
|
| 1999 |
Kitamura M, Ohmori K, Kawase T, Suzuki K. Total Synthesis of Pradimicinone, the Common Aglycon of the Pradimicin-Benanomicin Antibiotics. Angewandte Chemie (International Ed. in English). 38: 1229-1232. PMID 29711751 DOI: 10.1002/(Sici)1521-3773(19990503)38:9<1229::Aid-Anie1229>3.0.Co;2-B |
0.35 |
|
| 1999 |
Ohmori K, Kitamura M, Suzuki K. From Axial Chirality to Central Chiralities: Pinacol Cyclization of 2,2'-Biaryldicarbaldehyde to trans-9,10-Dihydrophenanthrene-9,10-diol. Angewandte Chemie (International Ed. in English). 38: 1226-1229. PMID 29711741 DOI: 10.1002/(Sici)1521-3773(19990503)38:9<1226::Aid-Anie1226>3.0.Co;2-T |
0.471 |
|
| 1999 |
Yamanoi S, Ohrui H, Seki K, Matsumoto T, Suzuki K. Alkylzirconation of alkynes catalyzed by triphenylcarbenium tetrakis(pentafluorophenyl)borate Tetrahedron Letters. 40: 8407-8410. DOI: 10.1016/S0040-4039(99)01795-5 |
0.323 |
|
| 1999 |
Kitamura M, Ohmori K, Suzuki K. Divergent behavior of cobalt- complexed enynehaving a leaving group Tetrahedron Letters. 40: 4563-4566. DOI: 10.1016/S0040-4039(99)00791-1 |
0.302 |
|
| 1999 |
Yamanoi S, Matsumoto T, Suzuki K. Reaction of 1-iodoalkynes with allylzirconiums: Generation of alkylidene carbenoid via allylzirconation Tetrahedron Letters. 40: 2793-2796. DOI: 10.1016/S0040-4039(99)00296-8 |
0.365 |
|
| 1999 |
Ohmori K, Kitamura M, Suzuki K. Von axialer zur Zentrochiralität: Pinakolcyclisierung eines 2,2′-Biaryldicarbaldehyds zumtrans-9,10-Dihydrophenanthren-9,10-diol Angewandte Chemie. 111: 1304-1307. DOI: 10.1002/(Sici)1521-3757(19990503)111:9<1304::Aid-Ange1304>3.0.Co;2-9 |
0.315 |
|
| 1998 |
Saito T, Suzuki T, Morimoto M, Akiyama C, Ochiai T, Takeuchi K, Matsumoto T, Suzuki K. Total Synthesis of the Furaquinocins Journal of the American Chemical Society. 120: 11633-11644. DOI: 10.1021/Ja982403T |
0.439 |
|
| 1998 |
Yamanoi S, Matsumoto T, Suzuki K. Regioselectivity of MAO-catalyzed allylmetallation of conjugated enynes with allylzirconiums Tetrahedron Letters. 39: 9727-9730. DOI: 10.1016/S0040-4039(98)02236-9 |
0.351 |
|
| 1998 |
Matsumoto T, Hamura T, Miyamoto M, Suzuki K. Base-promoted ring expansion of 2-alkoxy-2-vinylbenzocyclobutenol into substituted naphthalene derivatives Tetrahedron Letters. 39: 4853-4856. DOI: 10.1016/S0040-4039(98)00920-4 |
0.365 |
|
| 1997 |
Taya K, Nagasawa T, Suzuki K. Enantiopure Acetals of α-Alkynyl Carbonyl Compounds: Organoaluminum-Mediated 1,2-Shift of Cobalt-Complexed Alkynyl Group with Concomitant Capture by a Nucleophile Synlett. 1997: 304-306. DOI: 10.1055/S-1997-776 |
0.331 |
|
| 1997 |
Matsumoto T, Hamura T, Kuriyama Y, Suzuki K. Isochroman-3-ones via site-selective ring opening of benzocyclobutenones promoted by lithium tetramethylpiperidide and reaction with aromatic aldehydes Tetrahedron Letters. 38: 8985-8988. DOI: 10.1016/S0040-4039(97)10369-0 |
0.428 |
|
| 1997 |
Saito T, Suzuki T, Takeuchi K, Matsumoto T, Suzuki K. Implication and improvement of stereoselective methylenation of a chiral aldehyde related to total synthesis of the furaquinocins Tetrahedron Letters. 38: 3755-3758. DOI: 10.1016/S0040-4039(97)00746-6 |
0.439 |
|
| 1997 |
Yamanoi S, Imai T, Matsumoto T, Suzuki K. MAO-Catalyzed Allylzirconation of 1-Alkynes Tetrahedron Letters. 38: 3031-3034. DOI: 10.1016/S0040-4039(97)00527-3 |
0.361 |
|
| 1997 |
Matsumoto T, Yamaguchi H, Suzuki K. C-Glycosyl juglone in angucycline synthesis: Total synthesis of galtamycinone, common aglycon of C-glycosyl naphthacenequinone-type angucyclines Tetrahedron. 53: 16533-16544. DOI: 10.1016/S0040-4020(97)01034-X |
0.421 |
|
| 1997 |
Suzuki K, Imai T, Yamanoi S, Chino M, Matsumoto T. Unusual Regioselectivity in the Reductive Coupling of Alkynes and Allenes by Hydrozirconation and Zinca‐Claisen Rearrangement Angewandte Chemie. 36: 2469-2471. DOI: 10.1002/Anie.199724691 |
0.332 |
|
| 1996 |
Suzuki K, Hosoya T, Takashiro E, Yamamoto Y, Matsumoto T. Total Syntheses Of Be-12406 A And Its C(8)-Vinyl Analog Heterocycles. 42: 397-414. DOI: 10.3987/Com-95-S55 |
0.354 |
|
| 1996 |
Chino M, Liang GH, Matsumoto T, Suzuki K. Hydrozirconation of Allenyl Sulfide for Generating γ-Thio-substituted Allylzirconium Species and Its Reaction with Carbonyl Compounds Chemistry Letters. 1996: 231-232. DOI: 10.1246/Cl.1996.231 |
0.356 |
|
| 1996 |
Matsumoto T, Yamaguchi H, Suzuki K. Total Synthesis of Galtamycinone, the Common Aglycon of the C-Glycosyl Naphthacenequinone Antibiotics Synlett. 1996: 433-434. DOI: 10.1055/S-1996-5461 |
0.393 |
|
| 1996 |
Hosoya T, Ohashi Y, Matsumoto T, Suzuki K. On the stereochemistry of aryl C-glycosides: Unusual behavior of bis-TBDPS protected aryl C-olivosides Tetrahedron Letters. 37: 663-666. DOI: 10.1016/0040-4039(95)02227-9 |
0.366 |
|
| 1995 |
Matsumoto T, Sohma T, Yamaguchi H, Suzuki K. C-Glycosylation-Cycloaddition Approach toC-Glycosyl Juglones. Versatile Intermediates toward ArylC-Glycoside Antibiotics Chemistry Letters. 24: 677-678. DOI: 10.1246/Cl.1995.677 |
0.382 |
|
| 1995 |
Nagasawa T, Handa Y, Onoguchi Y, Ohba S, Suzuki K. Stereoselective Synthesis of Cyclopropanes via Homoallylic Participation Synlett. 1995: 739-741. DOI: 10.1246/Bcsj.69.31 |
0.495 |
|
| 1995 |
Nagasawa T, Kitamura M, Suzuki K. Cobalt-Complexation Makes 2-(1-Alkynyl)propenes Good Ene Donors in Carbonyl-Ene Reaction Synlett. 1995: 1183-1186. DOI: 10.1055/S-1995-5226 |
0.323 |
|
| 1995 |
Nagasawa T, Onoguchi Y, Matsumoto T, Suzuki K. Short-Step Total Synthesis of a Cyclopropane-Containing Eicosanoid Synlett. 1995: 1023-1024. DOI: 10.1055/S-1995-5189 |
0.44 |
|
| 1995 |
Hosoya T, Kuriyama Y, Suzuki K. Convenient Synthesis of Phthalides via Regioselective Baeyer-Villiger Oxidation of Benzocyclobutenones Synlett. 1995: 635-638. DOI: 10.1055/S-1995-5040 |
0.365 |
|
| 1995 |
Matsumoto T, Sohma T, Yamaguchi H, Kurata S, Suzuki K. Benzyne-Furan Cycloaddition Approach to the Angucyclines: First Total Synthesis of Antibiotic C104 Synlett. 1995: 263-266. DOI: 10.1055/S-1995-4936 |
0.407 |
|
| 1995 |
Hosoya T, Hasegawa T, Kuriyama Y, Matsumoto T, Suzuki K. [2+2] Cycloaddition of Benzyne and Ketene Silyl Acetal as an Efficient Route to Benzocyclobutenones Synlett. 1995: 177-179. DOI: 10.1055/S-1995-4913 |
0.382 |
|
| 1995 |
Saito T, Morimoto M, Akiyama C, Matsumoto T, Suzuki K. Stereocontrolled Convergent Total Synthesis of (.+-.)-Furaquinocin D Journal of the American Chemical Society. 117: 10757-10758. DOI: 10.1021/Ja00148A024 |
0.335 |
|
| 1995 |
Hosoya T, Hasegawa T, Kuriyama Y, Suzuki K. Stereospecificity in [2 + 2] cycloaddition of benzyne and ketene silyl acetal Tetrahedron Letters. 36: 3377-3380. DOI: 10.1016/0040-4039(95)00546-O |
0.405 |
|
| 1995 |
Maeta H, Nagasawa T, Handa Y, Takei T, Osamura Y, Suzuki K. Unexpected outcome of NbCl5-promoted Sakurai reaction: Mechanistic implications relevant to C4H7+ species Tetrahedron Letters. 36: 899-902. DOI: 10.1016/0040-4039(94)02332-6 |
0.329 |
|
| 1995 |
Matsumoto T, Sohma T, Yamaguchi H, Kurata S, Suzuki K. Total synthesis of antibiotic C104: Benzyne-Furan cycloaddition approach to the angucyclines Tetrahedron. 51: 7347-7360. DOI: 10.1016/0040-4020(95)00384-K |
0.416 |
|
| 1995 |
Suzuki K, Hasegawa T, Imai T, Maeta H, Ohba S. AgAsF6 as safe alternative to AgClO4 for generating cationic zirconocene species: Utilities in lewis acid-promoted selective CC bond forming reactions Tetrahedron. 51: 4483-4494. DOI: 10.1016/0040-4020(94)01135-M |
0.371 |
|
| 1994 |
Hosoya T, Takashiro E, Matsumoto T, Suzuki K. Total Synthesis of the Gilvocarcins Journal of the American Chemical Society. 116: 1004-1015. DOI: 10.5059/Yukigoseikyokaishi.53.1045 |
0.436 |
|
| 1994 |
Suzuki K. Total synthesis of aryl C-glycoside antibiotics Pure and Applied Chemistry. 66: 2175-2178. DOI: 10.1351/pac199466102175 |
0.38 |
|
| 1994 |
Suzuki K. Novel Lewis acid catalysis in organic synthesis Pure and Applied Chemistry. 66: 1557-1564. DOI: 10.1351/Pac199466071557 |
0.362 |
|
| 1994 |
Hosoya T, Takashiro E, Matsumoto T, Suzuki K. First total synthesis of BE-12406 A Tetrahedron Letters. 35: 4591-4594. DOI: 10.1016/S0040-4039(00)60738-4 |
0.384 |
|
| 1993 |
SUZUKI K, MATSUMOTO T. New Methods in Glycoside Synthesis by Using Early Transition Metal-Derived Reagent. Journal of Synthetic Organic Chemistry, Japan. 51: 718-732. DOI: 10.5059/Yukigoseikyokaishi.51.718 |
0.461 |
|
| 1993 |
Matsumoto T, Sohma T, Hatazaki S, Suzuki K. On the Regiochemistry of Cycloaddition of Unsymmetrical Aryne with Nitrone Remarkable Effect of Trialkylsilyl Substituent Synlett. 1993: 843-846. DOI: 10.1055/S-1993-22628 |
0.382 |
|
| 1993 |
Maeta H, Hasegawa T, Suzuki K. Hydrozirconation of Allenylstannane for Generating Bimetallic Three-Carbon Species: Synthesis of (E)-1,3-Dienes from Carbonyl Compounds Synlett. 1993: 341-343. DOI: 10.1055/S-1993-22448 |
0.317 |
|
| 1993 |
Nagasawa T, Suzuki K. [3+1] Synthetic Route Toward Synthesis of Cyclobutane/butene Derivatives Based on the Large α-Cation-Stabilizing Effect of Cyclopropane1 Synlett. 1993: 29-31. DOI: 10.1055/S-1993-22335 |
0.396 |
|
| 1993 |
Maeta H, Suzuki K. Two- and four-carbon homologation of aldehyde by AgClO4-catalyzed addition of alkoxyalkenylzirconocene chloride Tetrahedron Letters. 34: 341-344. DOI: 10.1016/S0040-4039(00)60583-X |
0.34 |
|
| 1992 |
SUZUKI K, NAGASAWA T. Recent Progress in O-Glycoside Synthesis-Methodological Aspects. Journal of Synthetic Organic Chemistry, Japan. 50: 378-390. DOI: 10.5059/Yukigoseikyokaishi.50.378 |
0.343 |
|
| 1992 |
Morooka M, Hashimoto T, Maeta H, Matsumoto T, Suzuki K, Ohba S. trans-1,3-Bis(diphenylphosphinoyl)cyclohexane Acta Crystallographica Section C-Crystal Structure Communications. 48: 1710-1712. DOI: 10.1107/S010827019200605X |
0.308 |
|
| 1992 |
Hashimoto T, Maeta H, Matsumoto T, Morooka M, Ohba S, Suzuki K. Synthesis of 1,3-bis(diphenylphosphinoyl)alkanes via double addition of diphenylphosphine to α,β-unsaturated carbonyl compounds : sequential 1,4- and 1,2-addition promoted by NbCl5-BF3.OEt2 Synlett. 1992: 340-342. DOI: 10.1055/S-1992-22007 |
0.383 |
|
| 1992 |
Tomooka K, Matsumoto K, Suzuki K, Tsuchihashi G. An Alternative Synthetic Route to the C(11)-C(17)-Fragment of Mycinolide IV Synlett. 1992: 129-130. DOI: 10.1055/S-1992-21289 |
0.544 |
|
| 1992 |
Suzuki K, Hashimoto T, Maeta H, Matsumoto T. Lewis Acid Promoted Reaction of Secondary Phosphines with Carbonyl Compounds: Remarkable Effect of Niobium(V) Chloride in Promoting an Intramolecular Oxidation-Reduction Process Synlett. 1992: 125-128. DOI: 10.1055/S-1992-21288 |
0.343 |
|
| 1992 |
Matsumoto T, Hosoya T, Suzuki K. Total synthesis and absolute stereochemical assignment of gilvocarcin M Journal of the American Chemical Society. 114: 3568-3570. DOI: 10.1021/Ja00035A069 |
0.331 |
|
| 1992 |
Maeta H, Suzuki K. New and highly (E)-selective synthesis of terminal 1,3-diene via three-carbon elongation of aldehyde Tetrahedron Letters. 33: 5969-5972. DOI: 10.1016/S0040-4039(00)61102-4 |
0.394 |
|
| 1992 |
Maeta H, Hashimoto T, Hasegawa T, Suzuki K. Grignard-type addition of alkenyl- and alkylzirconocene chloride to aldehyde: Remarkable catalytic acceleration effect of AgClO4 Tetrahedron Letters. 33: 5965-5968. DOI: 10.1016/S0040-4039(00)61101-2 |
0.326 |
|
| 1992 |
Suzuki K, Seebach D. threo-3-Alkyl- and -Arylglutamic Acid Derivatives by Michael Additions of Boc-BMI Li-Enolates to 2,6-Di-t-butyl-4-methoxyphenyl Alkenoates on the Diastereoselectivity of the Coupling of Trigonal Centers Involving Heterocyclic Li-Enolates Liebigs Annalen Der Chemie. 1992: 51-61. DOI: 10.1002/Jlac.199219920111 |
0.439 |
|
| 1991 |
Matsumoto T, Hosoya T, Suzuki K. O → C-Glycoside Rearrangement of Resorcinol Derivatives. Versatile Intermediates in the Synthesis of Aryl C-Glycosides Synlett. 1991: 709-711. DOI: 10.1055/S-1991-34769 |
0.394 |
|
| 1991 |
Matsumoto T, Katsuki M, Jona H, Suzuki K. Convergent total synthesis of vineomycinone B2 methyl ester and its C(12)-epimer Journal of the American Chemical Society. 113: 6982-6992. DOI: 10.1021/Ja00018A041 |
0.375 |
|
| 1991 |
Matsumoto T, Hosoya T, Katsuki M, Suzuki K. New efficient protocol for aryne generation. Selective synthesis of differentially protected 1,4,5-naphthalenetriols Tetrahedron Letters. 32: 6735-6736. DOI: 10.1016/S0040-4039(00)93589-5 |
0.38 |
|
| 1991 |
Matsumoto T, Jona H, Katsuki M, Suzuki K. Efficient method for introducing vineomycin-fridamycin-type side chain. Total synthesis of fridamycin E Tetrahedron Letters. 32: 5103-5106. DOI: 10.1016/S0040-4039(00)93439-7 |
0.4 |
|
| 1991 |
Matsumoto T, Kakigi H, Suzuki K. Ortho-metallation of anthracene derivative: problem and solution Tetrahedron Letters. 32: 4337-4340. DOI: 10.1016/S0040-4039(00)92164-6 |
0.319 |
|
| 1990 |
Shimazaki M, Morimoto M, Suzuki K. Stereoselective construction of three-and four-contiguous asymmetric centers : novel possibility by alkylative rearrangement of epoxy silyl ethers Tetrahedron Letters. 31: 3335-3338. DOI: 10.1016/S0040-4039(00)89058-9 |
0.493 |
|
| 1990 |
Mukaiyama T, Suzuki K, Yamada T, Tabusa F. 4-O-Benzyl-23-O-isopropylidene-L-threose: A useful building block for stereoselective synthesis of monosaccharides Tetrahedron. 46: 265-276. DOI: 10.1016/S0040-4020(01)97597-0 |
0.496 |
|
| 1989 |
Matsumoto T, Katsuki M, Suzuki K. RapidO-Glycosidation of Phenols with Glycosyl Fluoride by Using the Combinational Activator, Cp2HfCl2–AgClO4 Chemistry Letters. 18: 437-440. DOI: 10.1246/Cl.1989.437 |
0.363 |
|
| 1989 |
Suzuki K, Maeta H, Suzuki T, Matsumoto T. Cp2ZrCl2AgBF4 in Benzene: A new reagent system for rapid and highly selective α-mannoside synthesis from tetra-O-benzyl-d-mannosyl fluoride Tetrahedron Letters. 30: 6879-6882. DOI: 10.1016/S0040-4039(01)93378-7 |
0.387 |
|
| 1989 |
Matsumoto T, Katsuki M, Jona H, Suzuki K. Synthetic study toward vineomycins. Synthesis of c-aryl glycoside sector via Cp2HfCl2AgClO4-promoted tactics Tetrahedron Letters. 30: 6185-6188. DOI: 10.1016/S0040-4039(01)93337-4 |
0.463 |
|
| 1989 |
Matsumoto T, Katsuki M, Suzuki K. Cp2ZrCl2-AgClO4: Efficient promoter for the Friedel-Crafts approach to C-aryl glycosides Tetrahedron Letters. 30: 833-836. DOI: 10.1016/S0040-4039(01)80628-6 |
0.433 |
|
| 1989 |
Shimazaki M, Hara H, Suzuki K. Stereoselective reduction of α-cyclopropyl ketones and α-cyclopropyl aldols. Stereo-directing effect by α-trimethylsilyl group Tetrahedron Letters. 30: 5447-5450. DOI: 10.1016/S0040-4039(01)80590-6 |
0.322 |
|
| 1989 |
Shimazaki M, Hara H, Suzuki K. Stereospecific 1,2-rearrangement of cyclopropyl group. Synthesis of chiral α-cyclopropyl ketones and α-cyclopropyl aldols Tetrahedron Letters. 30: 5443-5446. DOI: 10.1016/S0040-4039(01)80589-X |
0.368 |
|
| 1989 |
Suzuki K, Maeta H, Matsumoto T. An improved procedure for metallocene-promoted glycosidation. Enhanced reactivity by employing 1:2-ratio of Cp2HfCl2-AgClO4 Tetrahedron Letters. 30: 4853-4856. DOI: 10.1016/S0040-4039(01)80526-8 |
0.34 |
|
| 1989 |
Tomooka K, Okinaga T, Suzuki K, Tsuchihashi G. Lactols in stereoselection 3 Tetrahedron Letters. 30: 1563-1566. DOI: 10.1016/S0040-4039(00)99520-0 |
0.59 |
|
| 1988 |
SUZUKI K. Highly Selective Acyclic Stereocontrol Based on 1, 2-Rearrangement Journal of Synthetic Organic Chemistry, Japan. 46: 367-377. DOI: 10.5059/Yukigoseikyokaishi.46.367 |
0.438 |
|
| 1988 |
Matsumoto T, Katsuki M, Suzuki K. New approach to C-aryl glycosides starting from phenol and glycosyl fluoride. Lewis acid-catalyzed rearrangement of O-glycoside to C-glycoside Tetrahedron Letters. 29: 6935-6938. DOI: 10.1016/S0040-4039(00)88479-8 |
0.361 |
|
| 1988 |
Suzuki K, Miyazawa M, Shimazaki M, Tsuchihashi G. Silicon-directed stereoselective synthesis of 2-vinyl-1,3-diols Tetrahedron. 44: 4061-4072. DOI: 10.1016/S0040-4020(01)86656-4 |
0.378 |
|
| 1988 |
Matsumoto T, Maeta H, Suzuki K, Gen-ichi Tsuchihashi l. First total synthesis of mycinamicin IV and VII. Tetrahedron Letters. 29: 3575-3578. DOI: 10.1016/0040-4039(88)85296-1 |
0.371 |
|
| 1988 |
Suzuki K, Maeta H, Matsumoto T, Tsuchihashi lG. New glycosidation reaction 2. preparation of 1-fluoro-d-desosamine derivative and its efficient glycosidation by the use of Cp2HfCl2-AgClO4 as the activator Tetrahedron Letters. 29: 3571-3574. DOI: 10.1016/0040-4039(88)85295-X |
0.379 |
|
| 1988 |
Matsumoto T, Maeta H, Suzuki K, Tsuchihashi lG. New glycosidation reaction 1 Tetrahedron Letters. 29: 3567-3570. DOI: 10.1016/0040-4039(88)85294-8 |
0.351 |
|
| 1987 |
Suzuki K, Matsumoto T, Tomooka K, Matsumoto K, Tsuchihashi G. Stereocontrolled First Total Synthesis of Mycinolide IV Chemistry Letters. 16: 113-116. DOI: 10.1246/Cl.1987.113 |
0.661 |
|
| 1987 |
Tomooka K, Matsuzawa K, Suzuki K, Tsuchihashi G. Lactols in stereoselection 2. Stereoselective synthesis of disubstituted cyclic ethers. Tetrahedron Letters. 28: 6339-6342. DOI: 10.1016/S0040-4039(01)91368-1 |
0.624 |
|
| 1987 |
Tomooka K, Okinaga T, Suzuki K, Tsuchihashi G. Lactols in stereoselection 1. Highly selective 1,4- and 1,5-asymmetric induction Tetrahedron Letters. 28: 6335-6338. DOI: 10.1016/S0040-4039(01)91367-X |
0.627 |
|
| 1987 |
Shimazaki M, Hara H, Suzuki K, Tsuchihashi G. On the use of epoxy alcohol-aldol rearrangement for stereoselective construction of quarternary carbon centers Tetrahedron Letters. 28: 5891-5894. DOI: 10.1016/S0040-4039(01)81083-2 |
0.322 |
|
| 1987 |
Suzuki K, Miyazawa M, Tsuchihashi G. Catalytic version of epoxy silyl ether rearrangements Tetrahedron Letters. 28: 3515-3518. DOI: 10.1016/S0040-4039(00)96341-X |
0.356 |
|
| 1986 |
Maruoka K, Hasegawa M, Yamamoto H, Suzuki K, Shimazaki M, Tsuchihashi G. Additions and Corrections. Epoxy Silyl Ether Rearrangements: A New, Stereoselective Approach to the Synthesis of β-Hydroxy Carbonyl Compounds Journal of the American Chemical Society. 108: 7134-7134. DOI: 10.1021/Ja00282A601 |
0.532 |
|
| 1986 |
Suzuki K, Tomooka K, Katayama E, Matsumoto T, Tsuchihashi G. Stereocontrolled asymmetric total synthesis of protomycinolide IV Journal of the American Chemical Society. 108: 5221-5229. DOI: 10.1021/Ja00277A028 |
0.644 |
|
| 1986 |
Maruoka K, Hasegawa M, Yamamoto H, Suzuki K, Shimazaki M, Tsuchihashi G. Epoxy silyl ether rearrangements: a new, stereoselective approach to the synthesis of .beta.-hydroxy carbonyl compounds Journal of the American Chemical Society. 108: 3827-3829. DOI: 10.1021/Ja00273A046 |
0.517 |
|
| 1986 |
Suzuki K, Miyazawa M, Shimazaki M, Tsuchihashi G. Stereo-divergent asymmetric total synthesis of avenaciolide and isoavenaciolide. Complete reversal of stereoselectivity in reduction of 2-vinyl aldols with / without trimethylsilyl directing group Tetrahedron Letters. 27: 6237-6240. DOI: 10.1016/S0040-4039(00)85441-6 |
0.462 |
|
| 1986 |
Suzuki K, Shimazaki M, Tsuchihashi G. Synthesis of 2-vinyl-1,3-diols via highly stereoselective reduction of 2-vinyl aldols using trimethylsilyl stereo-directing group Tetrahedron Letters. 27: 6233-6236. DOI: 10.1016/S0040-4039(00)85440-4 |
0.474 |
|
| 1986 |
Suzuki K, Masuda T, Fukazawa Y, Tsuchihashi G. C(2)-stereocontrol of δ-lactones acid-catalyzed cyclization of ketene dithioacetal having an internal hydroxyl group Tetrahedron Letters. 27: 3661-3664. DOI: 10.1016/S0040-4039(00)84875-3 |
0.384 |
|
| 1986 |
Suzuki K, Ohkuma T, Miyazawa M, Tsuchihashi G. Asymmetric synthesis of chiral synthons bearing alkynyl group organoaluminum-promoted pinacol-type rearrangement Tetrahedron Letters. 27: 373-376. DOI: 10.1016/S0040-4039(00)84022-8 |
0.447 |
|
| 1986 |
MARUOKA K, HASEGAWA M, YAMAMOTO H, SUZUKI K, SHIMAZAKI M, TSUCHIHASHI G. ChemInform Abstract: Epoxy Silyl Ether Rearrangements: A New, Stereoselective Approach to the Synthesis of β-Hydroxy Carbonyl Compounds. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198642112 |
0.534 |
|
| 1985 |
Suzuki K, Tomooka K, Shimazaki M, Tsuchihashi G. Conformational effects in organoaluminum-promoted pinacol-type rearrangement Tetrahedron Letters. 26: 4781-4784. DOI: 10.1016/S0040-4039(00)94950-5 |
0.556 |
|
| 1985 |
Suzuki K, Tomooka K, Matsumoto T, Katayama E, Tsuchihashi G. Stereoselective synthesis of C(1)–C(9) and C(11)–C(17)fragments of protomycinolide iv based on asymmetric pinacol-typerearrangement Tetrahedron Letters. 26: 3711-3714. DOI: 10.1016/S0040-4039(00)89230-8 |
0.628 |
|
| 1985 |
Suzuki K, Katayama E, Tomooka K, Matsumoto T, Tsuchihashi G. Highly stereoselective approach to chiral building block possessing three contiguous asymmetric centers. Preparation of four possible diastereomers of β,β′-dimethyl-bis-homoallylic alcohol derivative Tetrahedron Letters. 26: 3707-3710. DOI: 10.1016/S0040-4039(00)89229-1 |
0.595 |
|
| 1985 |
Suzuki K, Ohkuma T, Tsuchihashi G. Enantio- and diastereo-controlled synthesis of (+) - and (−) - eldanolide based on asymmetric pinacol-type rearrangement Tetrahedron Letters. 26: 861-864. DOI: 10.1016/S0040-4039(00)61949-4 |
0.426 |
|
| 1985 |
SUZUKI K, KATAYAMA E, TOMOOKA K, MATSUMOTO T, TSUCHIHASHI G. ChemInform Abstract: Highly Stereoselective Approach to Chiral Building Block Possessing Three Contiguous Asymmetric Centers. Three Continuous Asymmetric Centers. Preparation of Four Possible Diastereomers of β,β′-Di-methyl-bis-homoallylic Alcohol Derivat Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198552093 |
0.59 |
|
| 1985 |
TSUCHIHASHI G, TOMOOKA K, SUZUKI K. ChemInform Abstract: COMPLETELY STEREOSPECIFIC 1,2-MIGRATION OF ALKYL GROUPS IN DIETHYLALUMINUM CHLORIDE (ET2ALCL) PROMOTED PINACOL-TYPE REARRANGEMENT Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198504140 |
0.581 |
|
| 1984 |
Suzuki K, Katayama E, Tsuchihashi G. Asymmetric synthesis of optically pure α-methyl-β,γ-unsaturated ketones via triethylaluminum-mediated stereospecific pinacol rearrangement of alkenyl groups Tetrahedron Letters. 25: 1817-1820. DOI: 10.1016/S0040-4039(01)90049-8 |
0.359 |
|
| 1984 |
Tsuchihashi G, Tomooka K, Suzuki K. Completely stereospecific 1,2-migration of alkyl groups in Et2AlCl promoted pinacol-type rearrangement Tetrahedron Letters. 25: 4253-4256. DOI: 10.1016/S0040-4039(01)81409-X |
0.582 |
|
| 1984 |
Suzuki K, Katayama E, Tsuchihashi G. Enantio- and diastereomerically pure threo-homoallylic alcohols via highly stereoselective reduction of α-methyl-β,γ-unsaturated ketones Tetrahedron Letters. 25: 2479-2482. DOI: 10.1016/S0040-4039(01)81209-0 |
0.314 |
|
| 1984 |
Suzuki K, Katayama E, Matsumoto T, Tsuchihashi G. Reductive pinacol-type rearrangement of chiral α-mesyloxy ketones promoted by organoaluminum compounds Tetrahedron Letters. 25: 3715-3718. DOI: 10.1016/0040-4039(84)80113-6 |
0.349 |
|
| 1984 |
Tabusa F, Yamada T, Suzuki K, Mukaiyama T. A FORMAL TOTAL SYNTHESIS OF POLYOXIN J USING 4-O-BENZYL-2,3-O-ISOPROPYLIDENE-L-THREOSE AS A COMMON CHIRAL BUILDING BLOCK Chemistry Letters. 13: 405-408. DOI: 10.1002/Chin.198436338 |
0.442 |
|
| 1983 |
Suzuki K, Katayama E, Tsuchihashi G. Asymmetric pinacol-type rearrangement of α-hydroxy methanesulfonates promoted by triethylaluminum — preparation of optically pure α-aryl and α-vinyl ketones — Tetrahedron Letters. 24: 4997-5000. DOI: 10.1016/S0040-4039(01)99831-4 |
0.331 |
|
| 1983 |
MUKAIYAMA T, TABUSA F, SUZUKI K. ChemInform Abstract: THE STEREOSELECTIVE SYNTHESIS OF 2,3-CIS-DIHYDROXY-Γ-BUTYROLACTONES BY THE OXIDATION OF Γ-BUTENOLIDES WITH POTASSIUM PERMANGANATE-CROWN ETHER Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198336197 |
0.363 |
|
| 1983 |
MUKAIYAMA T, YUKI Y, SUZUKI K. ChemInform Abstract: THE STEREOSELECTIVE SYNTHESIS OF L-TAGATOSE - AN APPLICATION OF ZINC(II) MEDIATED HIGHLY STEREOSELECTIVE ADDITION OF 2-FURYLLITHIUM TO POLYOXYGENATED ALDEHYDE Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198306295 |
0.499 |
|
| 1983 |
SUZUKI K, IKEGAWA A, MUKAIYAMA T. ChemInform Abstract: THE ENANTIOSELECTIVE MICHAEL ADDITION OF THIOLS TO CYCLOALKENONES BY USING (2S,4S)-2-(ANILINOMETHYL)-1-ETHYL-4-HYDROXYPYRROLIDINE AS CHIRAL CATALYST Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198303114 |
0.442 |
|
| 1982 |
Suzuki K, Ikegawa A, Mukaiyama T. ASYMMETRIC SYNTHESIS OF OPTICALLY ACTIVE CYCLOHEXENOL DERIVATIVES VIA HIGHLY STEREOSELECTIVE REDUCTION OF (R)-3-(p-t-BUTYLPHENYLTHIO) CYCLOHEXAN-1-ONE Chemistry Letters. 11: 899-902. DOI: 10.1246/Cl.1982.899 |
0.409 |
|
| 1982 |
Suzuki K, Mukaiyama T. A NOVEL METHOD FOR THE SYNTHESIS OF 2-DEOXYDISACCHARIDE BY STEREOSELECTIVE CYCLIZATION OF THE ACYCLIC PRECURSOR Chemistry Letters. 11: 683-686. DOI: 10.1246/Cl.1982.683 |
0.467 |
|
| 1982 |
Suzuki K, Ikegawa A, Mukaiyama T. The Enantioselective Michael Addition of Thiols to Cycloalkenones by Using (2S, 4S)-2-Anilinomethyl-1-ethyl-4-hydroxypyrrolidine as Chiral Catalyst Bulletin of the Chemical Society of Japan. 55: 3277-3282. DOI: 10.1246/Bcsj.55.3277 |
0.464 |
|
| 1982 |
Mukaiyama T, Suzuki K, Yamada T. 4-O-BENZYL-2,3-O-ISOPROPYLIDENE-L-THREOSE —A NEW AND USEFUL BUILDING BLOCK FOR THE SYNTHESES OF L-SUGARS— Chemistry Letters. 11: 929-932. DOI: 10.1002/Chin.198250327 |
0.389 |
|
| 1981 |
Mukaiyama T, Ikegawa A, Suzuki K. HIGHLY ENANTIOSELECTIVE MICHAEL ADDITION OF THIOLS TO 2-CYCLOHEXENONE BY USING (2S,4S)-2-(ANILINOMETHYL)-1-ETHYL-4-HYDROXYPYRRQLIPINE AS A CHIRAL CATALYST Chemistry Letters. 10: 165-168. DOI: 10.1246/Cl.1981.165 |
0.446 |
|
| 1981 |
Suzuki K, Yuki Y, Mukaiyama T. THE STEREOSELECTIVE SYNTHESIS OF D-RIBULOSE Chemistry Letters. 10: 1529-1532. DOI: 10.1002/Chin.198221307 |
0.396 |
|
| 1980 |
Mukaiyama T, Suzuki K. ASYMMETRIC ADDITION OF ACETYLIDE TO ALIPHATIC ALDEHYDES—PREPARATION OF OPTICALLY ACTIVE 5-OCTYL-2(5H)-FURANONE— Chemistry Letters. 9: 255-256. DOI: 10.1002/Chin.198043185 |
0.377 |
|
| 1979 |
Mukaiyama T, Soai K, Sato T, Shimizu H, Suzuki K. Enantioface-differentiating (asymmetric) addition of alkyllithium and dialkylmagnesium to aldehydes by using (2S,2'S)-2-hydroxymethyl-1-[(1-alkylpyrrolidin-2-yl)methyl]pyrrolidines as chiral ligands Journal of the American Chemical Society. 101: 1455-1460. DOI: 10.1021/Ja00500A015 |
0.438 |
|
| 1979 |
Mukaiyama T, Suzuki K, Soai K, Sato T. ENANTIOSELECTIVE ADDITION OF ACETYLENE TO ALDEHYDE. PREPARATION OF OPTICALLY ACTIVE ALKYNYL ALCOHOLS Chemistry Letters. 8: 447-448. DOI: 10.1002/Chin.198005101 |
0.421 |
|
| 1978 |
Sato T, Soai K, Suzuki K, Mukaiyama T. ENANTIOFACE-DIFFERENTIATING (ASYMMETRIC) ADDITION OF DIALKYLMAGNESIUM TO ALDEHYDES BY USING THE LITHIUM SALT OF (2S, 2′S)-2-HYDROXYMETHYL-1-[(1-METHYLPYRPOLIDIN-2-YL)METHYL]PYRROLIDINE AS A CHIRAL LIGAND Chemistry Letters. 7: 601-604. DOI: 10.1246/Cl.1978.601 |
0.473 |
|
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