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Shuji Kanemasa

Shuji Kanemasa

D-Index & Metrics

Chemistry

D-Index
45
Citations
7943
World Ranking
16380
National Ranking
1289

Overview

Shuji Kanemasa is affiliated with Kyushu University in Japan. Their academic profile includes engagement primarily in research activities associated with this institution.

No specific data is available regarding recent papers by Shuji Kanemasa, including titles, years of publication, or publication venues.

There are no frequent co-authors or collaborative partnerships documented, indicating either independent research work or limited available metadata on collaborations.

Shuji Kanemasa's publication record does not list any recurrent venues for dissemination of research findings, which may suggest either a broad range of publication outlets or a lack of concentrated publication activity in specific journals or conferences.

The scientist has not recorded any book publications linked to particular publishers, nor is there information on the number or scope of such publications.

Information regarding main fields, subfields of study, or primary research topics is not provided, so no specific domains or areas of specialization can be identified within their scholarly profile.

There are no awards or honors listed, which may reflect either a lack of such recognitions or unreported data on these aspects.

Best Publications

  • Highly Enantioselective Catalytic Fluorination and Chlorination Reactions of Carbonyl Compounds Capable of Two‐Point Binding

    Norio Shibata;Junji Kohno;Kazumi Takai;Takehisa Ishimaru

  • Lewis Acid-Catalyzed Enantioselective Hydroxylation Reactions of Oxindoles and β-Keto Esters Using DBFOX Ligand

    Takehisa Ishimaru;Norio Shibata;Jun Nagai;Shuichi Nakamura

  • Transition-Metal Aqua Complexes of 4,6-Dibenzofurandiyl-2,2‘-bis(4-phenyloxazoline). Effective Catalysis in Diels−Alder Reactions Showing Excellent Enantioselectivity, Extreme Chiral Amplification, and High Tolerance to Water, Alcohols, Amines, and Acids

    Shuji Kanemasa;Yoji Oderaotoshi;Shin Ichi Sakaguchi;Hidetoshi Yamamoto

  • Recent Advances in Azomethine Ylide Chemistry

    Otohiko Tsuge;Shuji Kanemasa

  • Recent advances in synthetic applications of nitrile oxide cycloaddition (1981-1989)

    Shuji Kanemasa;Otohiko Tsuge

  • ASYMMETRIC CONJUGATE ADDITION OF THIOLS TO A 3-(2-ALKENOYL)-2-OXAZOLIDINONE CATALYZED BY THE DBFOX/PH AQUA COMPLEX OF NICKEL(II) PERCHLORATE

    Shuji Kanemasa;and Yoji Oderaotoshi;Eiji Wada

  • Lithium bromide-triethylamine induced cycloaddition of N-alkylidene 2-amino esters and amides to electron-deficient olefins with high regio- and stereoselectivity

    Otohiko Tsuge;Shuji Kanemasa;Manabu Yoshioka

  • Simple generation of nonstabilized azomethine ylides through decarboxylative condensation of α-amino acids with carbonyl compounds via 5-oxazolidinone intermediates

    Otohiko Tsuge;Shuji Kanemasa;Masayuki Ohe;Shigeori Takenaka

  • Highly Endo- and Enantioselective Asymmetric Nitrone Cycloadditions Catalyzed by the Aqua Complex of 4,6-Dibenzofurandiyl-2,2‘-bis(4-phenyl- oxazoline)−Nickel(II) Perchlorate. Transition Structure Based on Dramatic Effect of MS 4A on Selectivities

    Shuji Kanemasa;Yoji Oderaotoshi;Junji Tanaka;Eiji Wada

  • Cationic Aqua Complexes of the C2-Symmetric trans-Chelating Ligand (R,R)-4,6-Dibenzofurandiyl-2,2′-bis(4-phenyloxazoline). Absolute Chiral Induction in Diels-Alder Reactions Catalyzed by Water-Tolerant Enantiopure Lewis Acids

    Shuji Kanemasa;Yoji Oderaotoshi;Hidetoshi Yamamoto;Junji Tanaka

  • Desymmetrization-like catalytic enantioselective fluorination of malonates and its application to pharmaceutically attractive molecules.

    Dhande Sudhakar Reddy;Norio Shibata;Jun Nagai;Shuichi Nakamura

  • Enantioselective Michael Additions of Nitromethane by a Catalytic Double Activation Method Using Chiral Lewis Acid and Achiral Amine Catalysts

    Unknown

  • Chiral DBFOX/Ph complex catalyzed enantioselective nitrone cycloadditions to alpha,beta-unsaturated aldehydes.

    Moto Shirahase;Shuji Kanemasa;Yoji Oderaotoshi

  • Enantioselective Enol Lactone Synthesis under Double Catalytic Conditions

    Unknown

  • Cornerstone works for catalytic 1,3-dipolar cycloaddition reactions

    Shuji Kanemasa

  • A new general route to N-protonated azomethine ylides from N-(silylmethyl)amidines and -thioamides. Cycloaddition of synthetic equivalents of nitrile ylides

    Otohiko Tsuge;Shuji Kanemasa;Koyo Matsuda

  • Lewis acid-catalyzed nitrone cycloadditions to bidentate and tridentate α,β-unsaturated ketones. High rate acceleration, absolutely endo-selective and regioselective reactions

    Shuji Kanemasa;Takashi Uemura;Eiji Wada

  • Regioselective cycloadditions of N-protonated azomethine ylides and 2-azaallyl anions generated from N-(silylmethyl) thioimidates, synthetic equivalents of nonstabilized nitrile ylides

    Otohiko Tsuge;Shuji Kanemasa;Toshiaki Yamada;Koyo Matsuda

  • Enantioselective Michael addition reactions of malononitrile catalyzed by chiral Lewis acid and achiral amine catalysts

    Kennosuke Itoh;Yoji Oderaotoshi;Shuji Kanemasa

  • Stereochemical study on 1,3-dipolar cycloaddition reactions of heteroaromatic N-ylides with unsymmetrically substituted olefinic dipolarophiles

    Otohiko Tsuge;Shuji Kanemasa;Shigeori Takenaka

  • Stereoselectivity of Cydoaddition of N-(Cyanomethyl)- and N-(α-Cyanobenzyl)imines with Olefinic Dipolarophiles. Synthetic Equivalents of Nitrile Ylide 1,3-Dipoles

    Otohiko Tsuge;Kazunori Ueno;Shuji Kanemasa;Kiyotaka Yorozu

  • Synthetic Versatility of N-(Silylmethyl)imines: Water-Induced Generation of N-Protonated Azomethine Ylides of Nonstabilized Type and Fluoride-Induced Generation of 2-Azaallyl Anions

    Otohiko Tsuge;Shuji Kanemasa;Akira Hatada;Koyo Matsuda

Frequent Co-Authors

Dennis P. Curran
Dennis P. Curran University of Pittsburgh
Hideo Nagashima
Hideo Nagashima Kyushu University
Takashi Hayashi
Takashi Hayashi Osaka University

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