Shimbayashi T, Nakamoto D, Okamoto K, Ohe K |
Shimbayashi T, Nakamoto D, Okamoto K, Ohe K |
Shimbayashi T, Nakamoto D, Okamoto K, Ohe K |
Facile Construction of Tetrahydropyrrolizines by Iron-Catalyzed Double Cyclization of Alkene-Tethered Oxime Esters with 1,2-Disubstituted Alkenes. |
Facile Construction of Tetrahydropyrrolizines by Iron-Catalyzed Double Cyclization of Alkene-Tethered Oxime Esters with 1,2-Disubstituted Alkenes. |
Facile Construction of Tetrahydropyrrolizines by Iron-Catalyzed Double Cyclization of Alkene-Tethered Oxime Esters with 1,2-Disubstituted Alkenes. |
Organic letters |
Organic letters |
Organic letters |
2018/05 |
Refereed |
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Disclose to all |
Shimbayashi T, Okamoto K, Ohe K |
Shimbayashi T, Okamoto K, Ohe K |
Shimbayashi T, Okamoto K, Ohe K |
Iron-Catalyzed Aminative Cyclization/Intermolecular Homolytic Aromatic Substitution Using Oxime Esters and Simple Arenes. |
Iron-Catalyzed Aminative Cyclization/Intermolecular Homolytic Aromatic Substitution Using Oxime Esters and Simple Arenes. |
Iron-Catalyzed Aminative Cyclization/Intermolecular Homolytic Aromatic Substitution Using Oxime Esters and Simple Arenes. |
Chemistry, an Asian journal, 13, 4, 395-399 |
Chemistry, an Asian journal, 13, 4, 395-399 |
Chemistry, an Asian journal, 13, 4, 395-399 |
2018/02 |
Refereed |
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Disclose to all |
Okamoto K, Nanya A, Eguchi A, Ohe K |
Okamoto K, Nanya A, Eguchi A, Ohe K |
Okamoto K, Nanya A, Eguchi A, Ohe K |
Asymmetric Synthesis of 2H-Azirines with a Tetrasubstituted Stereocenter by Enantioselective Ring Contraction of Isoxazoles. |
Asymmetric Synthesis of 2H-Azirines with a Tetrasubstituted Stereocenter by Enantioselective Ring Contraction of Isoxazoles. |
Asymmetric Synthesis of 2H-Azirines with a Tetrasubstituted Stereocenter by Enantioselective Ring Contraction of Isoxazoles. |
Angewandte Chemie (International ed. in English), 57, 4, 1039-1043 |
Angewandte Chemie (International ed. in English), 57, 4, 1039-1043 |
Angewandte Chemie (International ed. in English), 57, 4, 1039-1043 |
2018/01 |
Refereed |
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Disclose to all |
Shimbayashi T, Okamoto K, Ohe K |
Shimbayashi T, Okamoto K, Ohe K |
Shimbayashi T, Okamoto K, Ohe K |
Generation of Stable Ruthenium(IV) Ketimido Complexes by Oxidative Addition of Oxime Esters to Ruthenium(II): Reactivity Studies Based on Electronic Properties of the Ru-N Bond. |
Generation of Stable Ruthenium(IV) Ketimido Complexes by Oxidative Addition of Oxime Esters to Ruthenium(II): Reactivity Studies Based on Electronic Properties of the Ru-N Bond. |
Generation of Stable Ruthenium(IV) Ketimido Complexes by Oxidative Addition of Oxime Esters to Ruthenium(II): Reactivity Studies Based on Electronic Properties of the Ru-N Bond. |
Chemistry (Weinheim an der Bergstrasse, Germany), 23, 66, 16892-16897 |
Chemistry (Weinheim an der Bergstrasse, Germany), 23, 66, 16892-16897 |
Chemistry (Weinheim an der Bergstrasse, Germany), 23, 66, 16892-16897 |
2017/11 |
Refereed |
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Disclose to all |
Sakata N, Sasakura K, Matsushita G, Okamoto K, Ohe K |
Sakata N, Sasakura K, Matsushita G, Okamoto K, Ohe K |
Sakata N, Sasakura K, Matsushita G, Okamoto K, Ohe K |
Copper-Catalyzed Regio- and Stereoselective Iodocyanation and Dicyanation of Alkynes with Cyanogen Iodide. |
Copper-Catalyzed Regio- and Stereoselective Iodocyanation and Dicyanation of Alkynes with Cyanogen Iodide. |
Copper-Catalyzed Regio- and Stereoselective Iodocyanation and Dicyanation of Alkynes with Cyanogen Iodide. |
Organic letters, 19, 13, 3422-3425 |
Organic letters, 19, 13, 3422-3425 |
Organic letters, 19, 13, 3422-3425 |
2017/07 |
Refereed |
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Disclose to all |
Kischkewitz M, Okamoto K, Mück-Lichtenfeld C, Studer A |
Kischkewitz M, Okamoto K, Mück-Lichtenfeld C, Studer A |
Kischkewitz M, Okamoto K, Mück-Lichtenfeld C, Studer A |
Radical-polar crossover reactions of vinylboron ate complexes. |
Radical-polar crossover reactions of vinylboron ate complexes. |
Radical-polar crossover reactions of vinylboron ate complexes. |
Science (New York, N.Y.), 355, 6328, 936-938 |
Science (New York, N.Y.), 355, 6328, 936-938 |
Science (New York, N.Y.), 355, 6328, 936-938 |
2017/03 |
Refereed |
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Disclose to all |
Shimbayashi Takuya, Okamoto Kazuhiro, Ohe Kouichi |
Shimbayashi Takuya, Okamoto Kazuhiro, Ohe Kouichi |
Shimbayashi Takuya, Okamoto Kazuhiro, Ohe Kouichi |
C-H Activation Induced by Oxidative Addition of N-O Bonds in Oxime Esters: Formation of Rhodacycles and Cycloaddition with Alkynes |
C-H Activation Induced by Oxidative Addition of N-O Bonds in Oxime Esters: Formation of Rhodacycles and Cycloaddition with Alkynes |
C-H Activation Induced by Oxidative Addition of N-O Bonds in Oxime Esters: Formation of Rhodacycles and Cycloaddition with Alkynes |
ORGANOMETALLICS, 35, 11, 2026-2031 |
ORGANOMETALLICS, 35, 11, 2026-2031 |
ORGANOMETALLICS, 35, 11, 2026-2031 |
2016/06/13 |
Refereed |
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Disclose to all |
Okamoto K, Shimbayashi T, Yoshida M, Nanya A, Ohe K |
Okamoto K, Shimbayashi T, Yoshida M, Nanya A, Ohe K |
Okamoto K, Shimbayashi T, Yoshida M, Nanya A, Ohe K |
Synthesis of 2H-Azirines by Iridium-Catalyzed Decarboxylative Ring Contraction of Isoxazol-5(4H)-ones. |
Synthesis of 2H-Azirines by Iridium-Catalyzed Decarboxylative Ring Contraction of Isoxazol-5(4H)-ones. |
Synthesis of 2H-Azirines by Iridium-Catalyzed Decarboxylative Ring Contraction of Isoxazol-5(4H)-ones. |
Angewandte Chemie (International ed. in English), 55, 25, 7199-7202 |
Angewandte Chemie (International ed. in English), 55, 25, 7199-7202 |
Angewandte Chemie (International ed. in English), 55, 25, 7199-7202 |
2016/06 |
Refereed |
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Disclose to all |
Okamoto K, Shimbayashi T, Tamura E, Ohe K |
Okamoto K, Shimbayashi T, Tamura E, Ohe K |
Okamoto K, Shimbayashi T, Tamura E, Ohe K |
Indium-Catalyzed [2 + 2] Cycloaddition of Allylsilanes to Internal Alkynones. |
Indium-Catalyzed [2 + 2] Cycloaddition of Allylsilanes to Internal Alkynones. |
Indium-Catalyzed [2 + 2] Cycloaddition of Allylsilanes to Internal Alkynones. |
Organic letters, 17, 23, 5843-5845 |
Organic letters, 17, 23, 5843-5845 |
Organic letters, 17, 23, 5843-5845 |
2015/12 |
Refereed |
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Disclose to all |
Okamoto K, Sakata N, Ohe K |
Okamoto K, Sakata N, Ohe K |
Okamoto K, Sakata N, Ohe K |
Copper-Catalyzed Cyanation of Aryl- and Alkenylboronic Reagents with Cyanogen Iodide. |
Copper-Catalyzed Cyanation of Aryl- and Alkenylboronic Reagents with Cyanogen Iodide. |
Copper-Catalyzed Cyanation of Aryl- and Alkenylboronic Reagents with Cyanogen Iodide. |
Organic letters, 17, 19, 4670-4673 |
Organic letters, 17, 19, 4670-4673 |
Organic letters, 17, 19, 4670-4673 |
2015/10 |
Refereed |
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Disclose to all |
Murai Masahito, Okamoto Kazuhiro, Miki Koji, Ohe Kouichi |
Murai Masahito, Okamoto Kazuhiro, Miki Koji, Ohe Kouichi |
Murai Masahito, Okamoto Kazuhiro, Miki Koji, Ohe Kouichi |
Palladium-catalyzed three-component coupling reactions of 2-(cyanomethyl)phenol, aryl halides, and carbon monoxide |
Palladium-catalyzed three-component coupling reactions of 2-(cyanomethyl)phenol, aryl halides, and carbon monoxide |
Palladium-catalyzed three-component coupling reactions of 2-(cyanomethyl)phenol, aryl halides, and carbon monoxide |
TETRAHEDRON, 71, 26-27, 4432-4437 |
TETRAHEDRON, 71, 26-27, 4432-4437 |
TETRAHEDRON, 71, 26-27, 4432-4437 |
2015/07/01 |
Refereed |
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Disclose to all |
Okamoto K, Tamura E, Ohe K |
Okamoto K, Tamura E, Ohe K |
Okamoto K, Tamura E, Ohe K |
Stereoselective construction of 1,3-disilylcyclopentane derivatives by scandium-catalyzed [3+2] cycloaddition of allylsilanes to β-silylenones. |
Stereoselective construction of 1,3-disilylcyclopentane derivatives by scandium-catalyzed [3+2] cycloaddition of allylsilanes to β-silylenones. |
Stereoselective construction of 1,3-disilylcyclopentane derivatives by scandium-catalyzed [3+2] cycloaddition of allylsilanes to β-silylenones. |
Angewandte Chemie (International ed. in English), 53, 38, 10195-10199 |
Angewandte Chemie (International ed. in English), 53, 38, 10195-10199 |
Angewandte Chemie (International ed. in English), 53, 38, 10195-10199 |
2014/09 |
Refereed |
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Disclose to all |
Shimbayashi Takuya, Okamoto Kazuhiro, Ohe Kouichi |
Shimbayashi Takuya, Okamoto Kazuhiro, Ohe Kouichi |
Shimbayashi Takuya, Okamoto Kazuhiro, Ohe Kouichi |
Synthesis of Imidazoles and Pyrimidines Using Palladium-Catalyzed Decarboxylatiye Intramolecular Condensation of 1,2,4-Oxadiazol-5(4H)-ones |
Synthesis of Imidazoles and Pyrimidines Using Palladium-Catalyzed Decarboxylatiye Intramolecular Condensation of 1,2,4-Oxadiazol-5(4H)-ones |
Synthesis of Imidazoles and Pyrimidines Using Palladium-Catalyzed Decarboxylatiye Intramolecular Condensation of 1,2,4-Oxadiazol-5(4H)-ones |
SYNLETT, 25, 13, 1916-1920 |
SYNLETT, 25, 13, 1916-1920 |
SYNLETT, 25, 13, 1916-1920 |
2014/08 |
Refereed |
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|
Disclose to all |
K. Okamoto; T. Shimbayashi; E. Tamura; K. Ohe |
K. Okamoto; T. Shimbayashi; E. Tamura; K. Ohe |
K. Okamoto; T. Shimbayashi; E. Tamura; K. Ohe |
Palladium-catalyzed aza-wittig-type condensation of isoxazol-5(4H)-ones with aldehydes |
Palladium-catalyzed aza-wittig-type condensation of isoxazol-5(4H)-ones with aldehydes |
Palladium-catalyzed aza-wittig-type condensation of isoxazol-5(4H)-ones with aldehydes |
Chemistry - A European Journal, 20, 6, 1490-1494 |
Chemistry - A European Journal, 20, 6, 1490-1494 |
Chemistry - A European Journal, 20, 6, 1490-1494 |
2014 |
Refereed |
English |
|
Disclose to all |
K. Okamoto; M. Watanabe; A. Mashida; K. Miki; K. Ohe |
K. Okamoto; M. Watanabe; A. Mashida; K. Miki; K. Ohe |
K. Okamoto; M. Watanabe; A. Mashida; K. Miki; K. Ohe |
Rhodium-catalyzed reaction of 2 h -azirines with carbonyl-ene-yne compounds giving 1-furyl-2-aza-1,3-dienes |
Rhodium-catalyzed reaction of 2 h -azirines with carbonyl-ene-yne compounds giving 1-furyl-2-aza-1,3-dienes |
Rhodium-catalyzed reaction of 2 h -azirines with carbonyl-ene-yne compounds giving 1-furyl-2-aza-1,3-dienes |
Synlett, 24, 12, 1541-1544 |
Synlett, 24, 12, 1541-1544 |
Synlett, 24, 12, 1541-1544 |
2013/07 |
Refereed |
English |
|
Disclose to all |
K. Okamoto; E. Tamura; K. Ohe |
K. Okamoto; E. Tamura; K. Ohe |
K. Okamoto; E. Tamura; K. Ohe |
Acid-catalyzed direct conjugate alkenylation of α,β-unsaturated ketones |
Acid-catalyzed direct conjugate alkenylation of α,β-unsaturated ketones |
Acid-catalyzed direct conjugate alkenylation of α,β-unsaturated ketones |
Angewandte Chemie - International Edition, 52, 40, 10639-10643 |
Angewandte Chemie - International Edition, 52, 40, 10639-10643 |
Angewandte Chemie - International Edition, 52, 40, 10639-10643 |
2013 |
Refereed |
English |
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Disclose to all |
K. Okamoto; M. Watanabe; N. Sakata; M. Murai; K. Ohe |
K. Okamoto; M. Watanabe; N. Sakata; M. Murai; K. Ohe |
K. Okamoto; M. Watanabe; N. Sakata; M. Murai; K. Ohe |
Copper-catalyzed C-H cyanation of terminal alkynes with cyanogen iodide |
Copper-catalyzed C-H cyanation of terminal alkynes with cyanogen iodide |
Copper-catalyzed C-H cyanation of terminal alkynes with cyanogen iodide |
Organic Letters, 15, 22, 5810-5813 |
Organic Letters, 15, 22, 5810-5813 |
Organic Letters, 15, 22, 5810-5813 |
2013 |
Refereed |
English |
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Disclose to all |
M. Murai; S. Kitabata; K. Okamoto; K. Ohe |
M. Murai; S. Kitabata; K. Okamoto; K. Ohe |
M. Murai; S. Kitabata; K. Okamoto; K. Ohe |
Gold-catalysed cycloisomerisation reactions of 2-(2-propynyl)pyridine N-oxides leading to indolizinones  |
Gold-catalysed cycloisomerisation reactions of 2-(2-propynyl)pyridine N-oxides leading to indolizinones  |
Gold-catalysed cycloisomerisation reactions of 2-(2-propynyl)pyridine N-oxides leading to indolizinones  |
Chemical Communications, 48, 61, 7622-7624 |
Chemical Communications, 48, 61, 7622-7624 |
Chemical Communications, 48, 61, 7622-7624 |
2012 |
Refereed |
English |
|
Disclose to all |
K. Okamoto; Y. Omoto; H. Sano; K. Ohe |
K. Okamoto; Y. Omoto; H. Sano; K. Ohe |
K. Okamoto; Y. Omoto; H. Sano; K. Ohe |
Alkyne-coordinating tridentate ligands: Structural properties and reactivity of their rhodium complexes |
Alkyne-coordinating tridentate ligands: Structural properties and reactivity of their rhodium complexes |
Alkyne-coordinating tridentate ligands: Structural properties and reactivity of their rhodium complexes |
Dalton Transactions, 41, 36, 10926-10929 |
Dalton Transactions, 41, 36, 10926-10929 |
Dalton Transactions, 41, 36, 10926-10929 |
2012 |
Refereed |
English |
|
Disclose to all |
K. Okamoto; M. Watanabe; M. Murai; R. Hatano; K. Ohe |
K. Okamoto; M. Watanabe; M. Murai; R. Hatano; K. Ohe |
K. Okamoto; M. Watanabe; M. Murai; R. Hatano; K. Ohe |
Practical synthesis of aromatic nitriles via gallium-catalysed electrophilic cyanation of aromatic C-H bonds |
Practical synthesis of aromatic nitriles via gallium-catalysed electrophilic cyanation of aromatic C-H bonds |
Practical synthesis of aromatic nitriles via gallium-catalysed electrophilic cyanation of aromatic C-H bonds |
Chemical Communications, 48, 25, 3127-3129 |
Chemical Communications, 48, 25, 3127-3129 |
Chemical Communications, 48, 25, 3127-3129 |
2012 |
Refereed |
English |
|
Disclose to all |
K. Okamoto; A. Mashida; M. Watanabe; K. Ohe |
K. Okamoto; A. Mashida; M. Watanabe; K. Ohe |
K. Okamoto; A. Mashida; M. Watanabe; K. Ohe |
An unexpected disproportional reaction of 2H-azirines giving (1E,3Z)-2-aza-1,3-dienes and aromatic nitriles in the presence of nickel catalysts |
An unexpected disproportional reaction of 2H-azirines giving (1E,3Z)-2-aza-1,3-dienes and aromatic nitriles in the presence of nickel catalysts |
An unexpected disproportional reaction of 2H-azirines giving (1E,3Z)-2-aza-1,3-dienes and aromatic nitriles in the presence of nickel catalysts |
Chemical Communications, 48, 29, 3554-3556 |
Chemical Communications, 48, 29, 3554-3556 |
Chemical Communications, 48, 29, 3554-3556 |
2012 |
Refereed |
English |
|
Disclose to all |
K. Okamoto |
K. Okamoto |
K. Okamoto |
Palladium-catalyzed atom-efficient carbohalogenation of alkenes |
Palladium-catalyzed atom-efficient carbohalogenation of alkenes |
Palladium-catalyzed atom-efficient carbohalogenation of alkenes |
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 70, 8, 852-853 |
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 70, 8, 852-853 |
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 70, 8, 852-853 |
2012 |
Refereed |
English |
|
Disclose to all |
A. Tsuneishi; K. Okamoto; Y. Ikeda; M. Murai; K. Miki; K. Ohe |
A. Tsuneishi; K. Okamoto; Y. Ikeda; M. Murai; K. Miki; K. Ohe |
A. Tsuneishi; K. Okamoto; Y. Ikeda; M. Murai; K. Miki; K. Ohe |
Rhodium-catalyzed carbene-transfer reactions via thienylcarbene complexes generated from thiocarbamoyl-ene-yne compounds  |
Rhodium-catalyzed carbene-transfer reactions via thienylcarbene complexes generated from thiocarbamoyl-ene-yne compounds  |
Rhodium-catalyzed carbene-transfer reactions via thienylcarbene complexes generated from thiocarbamoyl-ene-yne compounds  |
Synlett, 5, 655-658 |
Synlett, 5, 655-658 |
Synlett, 5, 655-658 |
2011/03 |
Refereed |
English |
|
Disclose to all |
K. Okamoto; T. Oda; S. Kohigashi; K. Ohe |
K. Okamoto; T. Oda; S. Kohigashi; K. Ohe |
K. Okamoto; T. Oda; S. Kohigashi; K. Ohe |
Palladium-catalyzed decarboxylative intramolecular aziridination from 4h-isoxazol-5-ones leading to 1-azabicyclo[3.1.0]hex-2-enes |
Palladium-catalyzed decarboxylative intramolecular aziridination from 4h-isoxazol-5-ones leading to 1-azabicyclo[3.1.0]hex-2-enes |
Palladium-catalyzed decarboxylative intramolecular aziridination from 4h-isoxazol-5-ones leading to 1-azabicyclo[3.1.0]hex-2-enes |
Angewandte Chemie - International Edition, 50, 48, 11470-11473 |
Angewandte Chemie - International Edition, 50, 48, 11470-11473 |
Angewandte Chemie - International Edition, 50, 48, 11470-11473 |
2011 |
Refereed |
English |
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Disclose to all |
T. Nishimura; J. Wang; M. Nagaosa; K. Okamoto; R. Shintani; F.-Y. Kwong; W.-Y. Yu; A.S.C. Chan; T. Hayashi |
T. Nishimura; J. Wang; M. Nagaosa; K. Okamoto; R. Shintani; F.-Y. Kwong; W.-Y. Yu; A.S.C. Chan; T. Hayashi |
T. Nishimura; J. Wang; M. Nagaosa; K. Okamoto; R. Shintani; F.-Y. Kwong; W.-Y. Yu; A.S.C. Chan; T. Hayashi |
Rhodium-catalyzed asymmetric addition of arylboronic acids to β-phthaliminoacrylate esters toward the synthesis of β-amino acids |
Rhodium-catalyzed asymmetric addition of arylboronic acids to β-phthaliminoacrylate esters toward the synthesis of β-amino acids |
Rhodium-catalyzed asymmetric addition of arylboronic acids to β-phthaliminoacrylate esters toward the synthesis of β-amino acids |
Journal of the American Chemical Society, 132, 2, 464-+ |
Journal of the American Chemical Society, 132, 2, 464-+ |
Journal of the American Chemical Society, 132, 2, 464-+ |
2010/01/20 |
Refereed |
English |
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Disclose to all |
K. Okamoto; T. Hayashi; V.H. Rawal |
K. Okamoto; T. Hayashi; V.H. Rawal |
K. Okamoto; T. Hayashi; V.H. Rawal |
Electronic and steric tuning of chiral diene ligands for rhodium-catalyzed asymmetric arylation of imines |
Electronic and steric tuning of chiral diene ligands for rhodium-catalyzed asymmetric arylation of imines |
Electronic and steric tuning of chiral diene ligands for rhodium-catalyzed asymmetric arylation of imines |
Chemical Communications, 32, 4815-4817 |
Chemical Communications, 32, 4815-4817 |
Chemical Communications, 32, 4815-4817 |
2009 |
Refereed |
English |
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Disclose to all |
K. Okamoto; T. Hayashi; V.H. Rawal |
K. Okamoto; T. Hayashi; V.H. Rawal |
K. Okamoto; T. Hayashi; V.H. Rawal |
Simple chiral diene ligands provide high enantioselectivities in transition-metal-catalyzed conjugate addition reactions |
Simple chiral diene ligands provide high enantioselectivities in transition-metal-catalyzed conjugate addition reactions |
Simple chiral diene ligands provide high enantioselectivities in transition-metal-catalyzed conjugate addition reactions |
Organic Letters, 10, 19, 4387-4389 |
Organic Letters, 10, 19, 4387-4389 |
Organic Letters, 10, 19, 4387-4389 |
2008/10/02 |
Refereed |
English |
|
Disclose to all |
S. Sögel; N. Tokunaga; K. Sasaki; K. Okamoto; T. Hayashi |
S. Sögel; N. Tokunaga; K. Sasaki; K. Okamoto; T. Hayashi |
S. Sögel; N. Tokunaga; K. Sasaki; K. Okamoto; T. Hayashi |
Rhodium/chiral diene-catalyzed asymmetric 1,4-addition of arylboronic acids to arylmethylene cyanoacetates |
Rhodium/chiral diene-catalyzed asymmetric 1,4-addition of arylboronic acids to arylmethylene cyanoacetates |
Rhodium/chiral diene-catalyzed asymmetric 1,4-addition of arylboronic acids to arylmethylene cyanoacetates |
Organic Letters, 10, 4, 589-592 |
Organic Letters, 10, 4, 589-592 |
Organic Letters, 10, 4, 589-592 |
2008/02/21 |
Refereed |
English |
|
Disclose to all |
K. Okamoto; T. Hayashi |
K. Okamoto; T. Hayashi |
K. Okamoto; T. Hayashi |
Platinum-catalyzed generation of silylenes from hydrodisilanes and their addition to α,β-unsaturated ketones |
Platinum-catalyzed generation of silylenes from hydrodisilanes and their addition to α,β-unsaturated ketones |
Platinum-catalyzed generation of silylenes from hydrodisilanes and their addition to α,β-unsaturated ketones |
Chemistry Letters, 37, 1, 108-109 |
Chemistry Letters, 37, 1, 108-109 |
Chemistry Letters, 37, 1, 108-109 |
2008/01/05 |
Refereed |
English |
|
Disclose to all |
K. Okamoto; T. Hayashi |
K. Okamoto; T. Hayashi |
K. Okamoto; T. Hayashi |
Platinum-catalyzed addition of dimethylsilylene to β-methyl α-β-unsaturated ketones: γ-silylation forming 1-Oxa-2-silacyclohex-5-enes |
Platinum-catalyzed addition of dimethylsilylene to β-methyl α-β-unsaturated ketones: γ-silylation forming 1-Oxa-2-silacyclohex-5-enes |
Platinum-catalyzed addition of dimethylsilylene to β-methyl α-β-unsaturated ketones: γ-silylation forming 1-Oxa-2-silacyclohex-5-enes |
Organic Letters, 9, 24, 5067-5069 |
Organic Letters, 9, 24, 5067-5069 |
Organic Letters, 9, 24, 5067-5069 |
2007/11/22 |
Refereed |
English |
|
Disclose to all |
R. Shintani; K. Yashio; T. Nakamura; K. Okamoto; T. Shimada; T. Hayashi |
R. Shintani; K. Yashio; T. Nakamura; K. Okamoto; T. Shimada; T. Hayashi |
R. Shintani; K. Yashio; T. Nakamura; K. Okamoto; T. Shimada; T. Hayashi |
Rhodium-catalyzed asymmetric synthesis of indanones: Development of a new "axially chiral" bisphosphine ligand |
Rhodium-catalyzed asymmetric synthesis of indanones: Development of a new "axially chiral" bisphosphine ligand |
Rhodium-catalyzed asymmetric synthesis of indanones: Development of a new "axially chiral" bisphosphine ligand |
Journal of the American Chemical Society, 128, 9, 2772-2773 |
Journal of the American Chemical Society, 128, 9, 2772-2773 |
Journal of the American Chemical Society, 128, 9, 2772-2773 |
2006/03/08 |
Refereed |
English |
|
Disclose to all |
T. Hayashi; N. Tokunaga; K. Okamoto; R. Shintani |
T. Hayashi; N. Tokunaga; K. Okamoto; R. Shintani |
T. Hayashi; N. Tokunaga; K. Okamoto; R. Shintani |
Asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated aldehydes catalyzed by a chiral diene-rhodium complex |
Asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated aldehydes catalyzed by a chiral diene-rhodium complex |
Asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated aldehydes catalyzed by a chiral diene-rhodium complex |
Chemistry Letters, 34, 11, 1480-1481 |
Chemistry Letters, 34, 11, 1480-1481 |
Chemistry Letters, 34, 11, 1480-1481 |
2005/11/05 |
Refereed |
English |
|
Disclose to all |
R. Shintani; W.-L. Duan; K. Okamoto; T. Hayashi |
R. Shintani; W.-L. Duan; K. Okamoto; T. Hayashi |
R. Shintani; W.-L. Duan; K. Okamoto; T. Hayashi |
Palladium/chiral phosphine-olefin complexes: X-ray crystallographic analysis and the use in catalytic asymmetric allylic alkylation |
Palladium/chiral phosphine-olefin complexes: X-ray crystallographic analysis and the use in catalytic asymmetric allylic alkylation |
Palladium/chiral phosphine-olefin complexes: X-ray crystallographic analysis and the use in catalytic asymmetric allylic alkylation |
Tetrahedron Asymmetry, 16, 20, 3400-3405 |
Tetrahedron Asymmetry, 16, 20, 3400-3405 |
Tetrahedron Asymmetry, 16, 20, 3400-3405 |
2005/10/17 |
Refereed |
English |
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Disclose to all |
R. Shintani; K. Okamoto; T. Hayashi |
R. Shintani; K. Okamoto; T. Hayashi |
R. Shintani; K. Okamoto; T. Hayashi |
Carbon-carbon bond-forming enantioselective synthesis of chiral organosilicon compounds by rhodium/chiral diene-catalyzed asymmetric 1,4-addition reaction |
Carbon-carbon bond-forming enantioselective synthesis of chiral organosilicon compounds by rhodium/chiral diene-catalyzed asymmetric 1,4-addition reaction |
Carbon-carbon bond-forming enantioselective synthesis of chiral organosilicon compounds by rhodium/chiral diene-catalyzed asymmetric 1,4-addition reaction |
Organic Letters, 7, 21, 4757-4759 |
Organic Letters, 7, 21, 4757-4759 |
Organic Letters, 7, 21, 4757-4759 |
2005/10/13 |
Refereed |
English |
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Disclose to all |
R. Shintani; K. Okamoto; T. Hayashi |
R. Shintani; K. Okamoto; T. Hayashi |
R. Shintani; K. Okamoto; T. Hayashi |
Rhodium-catalyzed synthesis of indenols by regioselective coupling of alkynes with ortho-carbonylated arylboronic acids |
Rhodium-catalyzed synthesis of indenols by regioselective coupling of alkynes with ortho-carbonylated arylboronic acids |
Rhodium-catalyzed synthesis of indenols by regioselective coupling of alkynes with ortho-carbonylated arylboronic acids |
Chemistry Letters, 34, 9, 1294-1295 |
Chemistry Letters, 34, 9, 1294-1295 |
Chemistry Letters, 34, 9, 1294-1295 |
2005/09/05 |
Refereed |
English |
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Y. Otomaru; K. Okamoto; R. Shintani; T. Hayashi |
Y. Otomaru; K. Okamoto; R. Shintani; T. Hayashi |
Y. Otomaru; K. Okamoto; R. Shintani; T. Hayashi |
Preparation of C<sub>2</sub>-symmetric bicyclo[2.2.2]octa-2,5-diene ligands and their use for rhodium-catalyzed asymmetric 1,4-addition of arylboronic acids |
Preparation of C<sub>2</sub>-symmetric bicyclo[2.2.2]octa-2,5-diene ligands and their use for rhodium-catalyzed asymmetric 1,4-addition of arylboronic acids |
Preparation of C<sub>2</sub>-symmetric bicyclo[2.2.2]octa-2,5-diene ligands and their use for rhodium-catalyzed asymmetric 1,4-addition of arylboronic acids |
Journal of Organic Chemistry, 70, 7, 2503-2508 |
Journal of Organic Chemistry, 70, 7, 2503-2508 |
Journal of Organic Chemistry, 70, 7, 2503-2508 |
2005/04/01 |
Refereed |
English |
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R. Shintani; K. Okamoto; T. Hayashi |
R. Shintani; K. Okamoto; T. Hayashi |
R. Shintani; K. Okamoto; T. Hayashi |
Rhodium-catalyzed isomerization of α-arylpropargyl alcohols to indanones: Involvement of an unexpected reaction cascade |
Rhodium-catalyzed isomerization of α-arylpropargyl alcohols to indanones: Involvement of an unexpected reaction cascade |
Rhodium-catalyzed isomerization of α-arylpropargyl alcohols to indanones: Involvement of an unexpected reaction cascade |
Journal of the American Chemical Society, 127, 9, 2872-2873 |
Journal of the American Chemical Society, 127, 9, 2872-2873 |
Journal of the American Chemical Society, 127, 9, 2872-2873 |
2005/03/09 |
Refereed |
English |
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Disclose to all |
R. Shintani; K. Okamoto; Y. Otomaru; K. Ueyama; T. Hayashi |
R. Shintani; K. Okamoto; Y. Otomaru; K. Ueyama; T. Hayashi |
R. Shintani; K. Okamoto; Y. Otomaru; K. Ueyama; T. Hayashi |
Catalytic asymmetric arylative cyclization of alkynals: Phosphine-free rhodium/diene complexes as efficient catalysts |
Catalytic asymmetric arylative cyclization of alkynals: Phosphine-free rhodium/diene complexes as efficient catalysts |
Catalytic asymmetric arylative cyclization of alkynals: Phosphine-free rhodium/diene complexes as efficient catalysts |
Journal of the American Chemical Society, 127, 1, 54-55 |
Journal of the American Chemical Society, 127, 1, 54-55 |
Journal of the American Chemical Society, 127, 1, 54-55 |
2005/01/12 |
Refereed |
English |
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Disclose to all |
K. Okamoto; Y. Nishibayashi; S. Uemura; A. Toshimitsu |
K. Okamoto; Y. Nishibayashi; S. Uemura; A. Toshimitsu |
K. Okamoto; Y. Nishibayashi; S. Uemura; A. Toshimitsu |
Asymmetric carboselenenylation reaction of alkenes with aromatic compounds  |
Asymmetric carboselenenylation reaction of alkenes with aromatic compounds  |
Asymmetric carboselenenylation reaction of alkenes with aromatic compounds  |
Angewandte Chemie - International Edition, 44, 23, 3588-3591 |
Angewandte Chemie - International Edition, 44, 23, 3588-3591 |
Angewandte Chemie - International Edition, 44, 23, 3588-3591 |
2005 |
Refereed |
English |
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Disclose to all |
R. Shintani; A. Tsurusaki; K. Okamoto; T. Hayashi |
R. Shintani; A. Tsurusaki; K. Okamoto; T. Hayashi |
R. Shintani; A. Tsurusaki; K. Okamoto; T. Hayashi |
Highly chemo- and enantioselective arylative cyclization of alkyne-tethered electron-deficient olefins catalyzed by rhodium complexes with chiral dienes |
Highly chemo- and enantioselective arylative cyclization of alkyne-tethered electron-deficient olefins catalyzed by rhodium complexes with chiral dienes |
Highly chemo- and enantioselective arylative cyclization of alkyne-tethered electron-deficient olefins catalyzed by rhodium complexes with chiral dienes |
Angewandte Chemie - International Edition, 44, 25, 3909-3912 |
Angewandte Chemie - International Edition, 44, 25, 3909-3912 |
Angewandte Chemie - International Edition, 44, 25, 3909-3912 |
2005 |
Refereed |
English |
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N. Tokunaga; Y. Otomaru; K. Okamoto; K. Ueyama; R. Shintani; T. Hayashi |
N. Tokunaga; Y. Otomaru; K. Okamoto; K. Ueyama; R. Shintani; T. Hayashi |
N. Tokunaga; Y. Otomaru; K. Okamoto; K. Ueyama; R. Shintani; T. Hayashi |
C<sub>2</sub>-symmetric bicyclo[2.2.2]octadienes as chiral ligands: Their high performance in rhodium-catalyzed asymmetric arylation of N-tosylarylimines |
C<sub>2</sub>-symmetric bicyclo[2.2.2]octadienes as chiral ligands: Their high performance in rhodium-catalyzed asymmetric arylation of N-tosylarylimines |
C<sub>2</sub>-symmetric bicyclo[2.2.2]octadienes as chiral ligands: Their high performance in rhodium-catalyzed asymmetric arylation of N-tosylarylimines |
Journal of the American Chemical Society, 126, 42, 13584-13585 |
Journal of the American Chemical Society, 126, 42, 13584-13585 |
Journal of the American Chemical Society, 126, 42, 13584-13585 |
2004/10/27 |
Refereed |
English |
|
Disclose to all |