84. Kuki, S.; Futamura, T.; Suzuki, R.; Yamamoto, M.; Minakawa, M.; Kawatsura, M.
Palladium-catalyzed Regioselective Hydroalkylation of 2-Fluoroallyl Acetates: Synthesis of Vinylmalonic Acids Ester Derivatives
Synlett 2015, in press. DOI: 10.1055/s-0034-1380747
83. Isa, K.; Minakawa, M.; Kawatsura, M.
Palladium-catalyzed Amination of 2,3,3-Trifluoroallyl Esters: Synthesis of Trifluoromethylenamines by the Intramolecular Fluorine Shift and CF3 Group Construction
Chem. Commun. 2015, 51, 6761–6764. DOI: 10.1039/C5CC01212K
82. Kanazawa, Y.; Yokota, T.; Ogasa, H.; Watanabe, H.; Hanakawa, T.; Soga, S.; Kawatsura, M.
Chemoselective Amination of Bromoiodobenzenes with Diarylamines by Palladium/Xantphos or Ligand-free Copper Catalysts
Tetrahedron 2015, 71, 1395–1402. DOI: 10.1016/j.tet.2015.01.028
81. Minakawa, M.; Ishikawa, T.; Namioka, J.; Hirooka, S.; Zhou, B.; Kawatsura, M.
Iron-Catalyzed [2+2+2] Cycloaddition of Trifluoromethyl Group Substituted Unsymmetrical Internal Alkynes
RSC Adv. 2014, 4, 41353–41356. DOI: 10.1039/c4ra06973k
80. Munemori, D.; Tsuji, H.; Uchida, K.; Suzuki, T.; Isa, K.; Minakawa, M.; Kawatsura, M.
Copper-catalyzed Regioselective Allylic Cyanation of Allylic Compounds with Trimethylsilyl Cyanide
Synthesis 2014, 46, 2747–2750. DOI: 10.1055/s-0034-1378322
79. Kawatsura, M.; Terasaki, S.; Minakawa, M.; Hirakawa, T.; Ikeda, K.; Itoh, T.
Enantioselective Allylic Amination of Trifluoromethyl Group Substituted Racemic and Unsymmetrical 1,3-Disubstituted Allylic Esters by Palladium Catalysts
Org. Lett. 2014, 16, 2442–2445. DOI: 10.1021/ol5008229
Highlighted in Synfacts 2014, 10, 714 DOI: 10.1055/s-0034-1378262
78. Nomada, E.; Watanabe, H.; Yamamoto, M.; Udagawa, T.; Zhou, B.; Kobayashi, A.; Minakawa, M.;
Kawatsura, M.
Palladium-catalyzed Double Substitution of 3-Aryl-2-fluoroallyl Acetates with Phenols via C-F Bond Activation
Synlett 2014, 1725–1730. DOI: 10.1055/s-0033-1339106
77. Kawatsura, M.; Uchida, K.; Terasaki, S.; Tsuji, H.; Minakawa, M.; Itoh, T.
Ruthenium-Catalyzed Regio- and Enantioselective Allylic Amination of Racemic 1-Arylallyl Esters
Org. Lett. 2014, 16, 1470–1473 DOI: 10.1021/ol5002768
Highlighted in Synfacts 2014, 10, 509 DOI: 10.1055/s-0033-1341175
76.Yamamoto, M.; Hayashi, S.; Isa, K.; Kawatsura, M.
Palladium-Catalyzed Double Alkylation of 3-Aryl-2-fluoroallyl Esters with Malonate Nucleophiles through the Carbon-Fluorine Bond Cleavage
Org. Lett. 2014, 16, 700–703 DOI: 10.1021/ol500121z
75.Hirakawa, T.; Kawatsura, M.; Itoh, T.
Regioselective Synthesis of Trifluoromethyl Group Containing Allylic Amines using Palladium-catalyzed Allylic Amination Pathway
J. Fluorine Chem. 2013, 152, 62–69 DOI: 10.1016/j.jfluchem.2013.03.008
74.Ibara, C.; Fujiwara, M.; Hayase, S.; Kawatsura, M.; Itoh, T.
Development of Sequential Type Iron Salt-catalyzed Nazarov/Michael Reaction in an Ionic Liquid Solvent System
Sci. China Chem. 2012, 55, 1628–1632 DOI: 10.1007/s11426-012-4629-3
73.Yoshimura, K.; Matsumoto, K.; Uetani, Y.; Sakumichi, S.; Hayase, S.; Kawatsura, M.; Itoh, T.
Thiophene-Substituted Fulleropyrrolidine Derivatives as Acceptor Molecules in a Thin Film Organic Solar Cell
Tetrahedron 2012, 68, 3605–3610 DOI: 10.1016/j.tet.2012.02.080
72.Ohira, K.; Abe, Y.; Kawatsura, M.; Suzuki, K.; Mizuno, M.; Amano, Y.; Itoh, T.
Design of Cellulose Dissolving Ionic Liquids Inspired by Nature
ChemSusChem 2012, 5,388-391 DOI: 10.1002/cssc.201100427
71.Abe, Y.; Yagi, Y.; Hayase, S.; Kawatsura, M.; Itoh, T.
Ionic Liquid Technology for Lipase-mediated Optical Resolution of Secondary Alcohols: Design of Ionic Liquids Applicable to Ionic Lequid Coated-Lipase Catalyzed Reaction
Ind. Eng. Chem. Res. 2012, 51, 9952–9958 DOI: 10.1021/ie202740u
70.Hirakawa, T.; Ikeda, K.; Ikeda, D.; Tanaka, T.; Ogasa, H.; Kawatsura, M.; Itoh, T.
Regioselective Synthesis of Trifluoromethyl Group-substituted Allylic Amines by Palladium-catalyzed Allylic Amination and Sequential Isomerization
Tetrahedron 2011, 67, 8238–8247 DOI: 10.1016/j.tet.2011.08.093
Highlighted in Synfacts 2012, 8, 73
69.Nakano, T.; Yagi, Y.; Miyahara, M.; Kamimura, A.; Kawatsura, M.; Itoh, T.
Chemo-Enzymatic Synthesis of a Multi-useful Chiral Building Block Molecule for the Synthesis of Medicinal Compounds
Molecules 2011, 16, 6747–6757 DOI: 10.3390/molecules16086747
68.Kawatsura, M.; Tsuji, H.; Uchida, K.; Itoh, T.
Iridium-catalyzed Allylic Alkylation of Monosubstituted Allylic Acetates with Azlactone, and Separation of Diastereoisomers by Sequential Aza-Cope Rearrangement
Tetrahedron 2011, 67, 7686–7691 DOI: 10.1016/j.tet.2011.08.016
67.Kawatsura, M.; Nobuto, H.; Hayashi, S.; Hirakawa, T.; Ikeda, D.; Itoh, T.
Palladium-catalyzed Regio- and Diastereoselective Allylic Alkylation in Ionic Liquids
Chem. Lett. 2011, 40, 953–955 DOI: 10.1246/cl.2011.953
66.Kawatsura, M.; Sato, M.; Tsuji, H.; Ata, F.; Itoh, T.
Retention of Regiochemistry and Chirality in the Ruthenium Catalyzed Allylic Alkylation of Disubstituted Allylic Esters
J. Org. Chem. 2011, 76, 5485–5488 DOI: 10.1021/jo2007169
65.Kawatsura, M.; Namioka, J.; Kajita, K.; Yamamoto, M.; Tsuji, H.; Itoh, T.
Ruthenium-catalyzed Regioselective Addition of Carboxylic Acids to Aryl and Trifluoromethyl Group Substituted Unsymmetrical Internal Alkynes
Org. Lett. 2011, 13, 3285–3287 DOI: 10.1021/ol201238u
64.Kude, K.; Hayase, S.; Kawatsura, M.; Itoh, T.
Iron-catalyzed Quick Homocoupling Reaction of Aryl or Alkynyl Grignard Reagents Using a Phosphonium Ionic Liquid Solvent System
Heteroatom Chem. 2011, 22, 397–404
63.Kawatsura, M.; Yamamoto, M.; Namioka, J.; Kajita, K.; Hirakawa, T.; Itoh, T.
Ruthenium-catalyzed Regioselective [2 + 2 + 2] Cyclotrimerization of Trifluoromethyl Group Substituted Internal Alkynes
Org. Lett. 2011, 13, 1001–1003 DOI: 10.1021/ol1030734
62.Hirakawa, T.; Ikeda, K.; Ogasa, H.; Kawatsura, M.; Itoh, T.
Regioselective Synthesis of Optically Active Trifluoromethyl Group Substituted Allylic Amines by Palladium-catalyzed Allylic Amination
Synlett 2010, 2887–2890
61.Abe, Y.; Yoshiyama, K.; Yagi, Y.; Hayase, S.; Kawatsura, M.; Itoh, T.
A Rational Design of Phosphonium Salt Type Ionic Liquids for Ionic Liquid Coated-Lipase Catalyzed Reaction
Green Chem. 2010, 12, 1976–1980
60.Matsumoto, K.; Hashimoto, K.; Hayase, S.; Kawatsura, M.; Itoh, T.
Design of Fulleropyrrolidine Derivatives as an Acceptor Molecule in a Thin Layer Organic Solar Cell
J. Mater. Chem. 2010, 20, 9226–9230
59.Kawatsura, M.; Kamesaki, K.; Yamamoto, M.; Hayase, S.; Itoh, T.
Homogeneous Ruthenium Precatalyst for Suzuki-Miyaura Coupling Reaction
Chem. Lett. 2010, 1050–1051
58.Ibara, C.; Fujiwara, M.; Hayase, S.; Kawatsura, M.; Nanjo, M.; Itoh, T.
Iron Salt-catalyzed One Pot Nazarov/Michael Reaction in an Ionic Liquid Solvent System.
ECS Transactions 2010, 28, 1–4
57.Kobayashi, J.; Matsui, S.; Ogiso, K.; Fujiwara, M.; Hayase, S.; Kawatsura, M.; Itoh, T.
Iron Salt-catalyzed Cascade Type One Pot Double Alkylation of Indole with Vinyl Ketones
Tetrahedron 2010, 66, 3917–3922
56.Kawatsura, M.; Hayashi, S.; Komatsu, Y.; Hayase, S.; Itoh, T.
Enantioselective a-Fluorination and Chlorination of b-Ketoesters by Cobalt Catalyst
Chem. Lett. 2010, 466–467
55.Kawatsura, M.; Kajita, K.; Hayase, S.; Itoh, T.
Iron- or Cobalt-catalyzed Nazarov Cyclization: Asymmetirc Reaction, and Tandem Cyclization/Fluorination Reaction
Synlett 2010, 1243-1246
54.Itoh,T.; Kanbara, M.; Nakajima,S.; Sakuta, Y.; Hayase, S.; Kawatsura, M.; Kato, T.; Miyazawa, K.; Uno, H.
Chemo-enzymatic Synthesis of Spiro Type gem-Difluorocyclopropane as Core Molecule Candidate for Liquid Crystal Compounds
J. Fluorine Chem. 2009, 130, 1157-1163
53.Itoh, T.; Watanabe, N.; Inada K.; Ishioka, A.; Hayase, S.; Kawatsura, M.; Minami, I.; Mori, S.
Design of Alkylsulfate Ionic Liquids for Lubricants
Chem. Lett. 2009, 38, 64–65
52.Fujiwara, M.; Kawatsura, M.; Hayase, S.; Nanjo, M.; Itoh, T.
Iron(III) salt-catalyzed Nazarov Cyclization/Michael addition of pyrrole derivatives
Adv. Synth. Catal. 2009, 351, 123–128
51.Itoh, T.; Kude, K.; Ishioak, A.; Hayase, S.; Kawatsura, M.
Development of Novel Phosphonium Ionic Liquid for Grignard Reaction: Iron Salt-catalyzed Rapid Homocoupling Reaction of Aryl Grignard Reagents
ECS Transactions, 2008, 20, 47–49
50.Abe, Y.; Hirakawa, T.; Nakajima, S.; Okano, N.; Hayase, S.; Kawatsura, M.; Hirose, Y.; Itoh, T.
Remarkable Activation of an Enzyme by (R)-Pyrrolidine-substituted Imidazolium Alkyl PEG Sulfate
Adv. Synth. Catal. 2008, 350, 1954–1958
49.Kawatsura, M.; Ata, F.; Hirakawa, T.; Hayase, S.; Itoh, T.
Linear Selective Allylic Amination of Allyl Acetates by Ruthenium Catalyst
Tetrahedron Lett. 2008, 49, 4873–4875
48.Kawatsura, M.; Fujiwara, M.; Nomura, S.; Uehara, H.; Hayase, S.; Itoh, T.
Multi-point Alkylation of Pyrrole with Vinyl Ketones Using Iron Salts as Catalyst
Chem. Lett. 2008, 37, 794–795
47.Taniguchi, T.; Fukuba, T.; Nakatsuka, S.; Hayase, S.; Kawatsura, M.; Uno, H.; Itoh, T.
Linker-oriented Design of Binaphthol Derivatives for Optical Resolution Using Lipase-catalyzed Reaction
J. Org. Chem. 2008, 73, 3875–3884
46.Kawatsura, M.; Hirakawa, T.; Tanaka, T.; Ikeda, D.; Hayase, S.; Itoh, T.
Regioselective Synthesis of Trifluoromethyl Group Substituted Allylic Amines via Palladium Catalyzed Allylic Amination
Tetrahedron Lett. 2008, 49, 2450–2453
45.Kawatsura, M.; Komatsu, Y.; Yamamoto, M.; Hayase, S.; Itoh, T.
Asymmetric Conjugate Addition of Thiols to (E)-3-Crotonoyloxazolidin-2-one by Iron- or Cobalt/pybox Catalyst
Tetrahedron 2008, 64, 3488–3493
44.Kawatsura, M.; Higuchi, Y.; Hayase, S.; Nanjo, M.; Itoh, T.
Iron(III) Chloride Catalyzed Nazarov Cyclization of 3-Substituted Thiophenes
Synlett 2008, 1009–1012
43.Itoh, T.; Mishiro, M.; Matsumoto, K.; Hayase, S.; Kawatsura, M.; Morimoto, M.
Synthesis of Fulleropyrrolidine Imidazolium-Salt Hybrids and their Solubility in Various Organic Solvents Solubility Control of Fullerene Derivatives Using Imidazolium-Salt Moiety as Functional Group Connector
Tetrahedron 2008, 64, 1823–1828
42.Abe, Y.; Kude, K.; Hayase, S.; Kawatsura, M.; Tsunashima, K.; Itoh, T.
Design of Phosphonium Ionic liquids Lipase-Catalyzed Transesterification
J. Mol. Catal. B: Enzym. 2008, 51, 81-85
41.Shi-Hun, H.; Hirakawa, T.; Fukuba, T.; Hayase, S.; Kawatsura, M.; Itoh, T.
Synthesis of Optically Pure Cycloalkenols via Combination Strategy of Enzyme-catalyzed Reaction and RCM Reaction
Tetrahedron Asymmetry 2007, 18, 2484–2490
40.Itoh, T.; Kude, K.; Hayase, S.; Kawatsura, M.
Design of Ionic Liquids as a Reaction Medium for the Grignard Reaction
Tetrahedron Lett. 2007, 48, 7774–7777
39.Kawatsura, M.; Ata, F.; Hayase, S.; Itoh, T.
Retention of Regiochemistry of Monosubstituted Allyl Acetates in the Ruthenium Catalyzed Allylic Alkylation
Chem. Commun. 2007, 4283–4285
38.Kawatsura, M.; Komatsu, Y.; Yamamoto, M.; Hayase, S.; Itoh, T.
Enantioselective C-S Bond Formation by Iron/pybox Catalyzed Michael Addition of Thiols to (E)-3-Crotonoyloxazolidin-2-one
Tetrahedron Lett. 2007, 48, 6480–6482
37.Kawatsura, M.; Ikeda, D.; Komatsu, Y.; Mitani, K.; Tanaka, T.; Uneishi, J.
Palladium-catalyzed Regio- and Diastereo-selective Allylic Alkylation using 2-(Diphenylphosphino)benzoic acid: Construction of Vicinal Quaternary and Tertiary Carbon Centers
Tetrahedron 2007, 63, 8815–8824
36.Itoh, T.; Kanbara, M.; Ohashi, M.; Hayase, S.; Kawatsura, M.; Kato, T.; Miyazawa, K.; Takagi, Y.; Uno, H.
gem-Difluorocyclopropane as Core Molecule Candidate for Liquid Crystal Compounds
J. Fluorine Chem. 2007, 128, 1112-1120
35.Kawatsura, M.; Aburatani. S.; Uenishi, J.
Catalytic Conjugate Addition of Heterocyclic Compounds to α,β-Unsaturated Carbonyl Compounds by Hafnium Salts and Scandium Salts
Tetrahedron 2007, 63, 4172-4177
34.Aburatani. S.; Kawatsura, M.; Uenishi, J.
Hafnium Chloride Catalyzed Conjugate Addition of Pyrrole, Pyrazole and Imidazole to α,β-Unsaturated Ketones
Heterocycles 2007, 71, 189-196
33.Itoh, T.; Uehara, H.; Ogiso, K.; Nomura, S.; Hayase, S.; Kawatsura, M.
Alkylation of N-Protecting Group Free Indole with Vinyl Ketones Using Iron Salt Catalyst
Chem. Lett. 2007, 50-51
32.Kawatsura, M.; Ata, F.; Wada, S.; Hayase, S.; Uno, H.; Itoh, T.
Ruthenium-catalysed Linear-selective Allylic Alkylation of Allyl Acetates
Chem. Commun. 2007, 298-300
31.Itoh, T.; Matsushita, Y.; Abe, Y.; Han, S-H.; Wada, S.; Hayase, S.; Kawatsura, M.; Takai, S.; Morimoto, M.; Hirose, Y.
Enhanced Enantioselectivity and Remarkable Acceleration of Lipase-Catalyzed Transesterification Using an Imizadolium PEG-alkyl Sulfate Ionic Liquid
Chem. Eur. J. 2006, 12, 9228-9237
30.Uehara, H.; Nomura, S.; Hayase, S.; Kawatsura, M.; Itoh, T.
A Novel 1,4-Addition Type Reaction of β-Keto Esters with Vinyl Ketones Catalyzed by Iron(II)tetrafluoroborate in an Ionic Liquid Solvent System
Electrochemistry 2006, 74, 635-638
29.Kawatsura, M.; Wada, S.; Hayase, S.; Itoh, T.
Palladium-catalyzed Regioselective Allylic Alkylation of 1-Aryl-2,3,3-trifluoroallyl Acetates
Synlett 2006, 2483-2485
28.Kawatsura, M.; Ikeda, D.; Ishii, T.; Komatsu, Y.; Uenishi, J.
Palladium-catalyzed Regio- and Diastereoselective Allylic Alkylation with Azlactones using Triphenylarsine
Synlett 2006, 2435-2438
27.Tsukada, Y.; Iwamoto, K.; Furutani, H.; Matsushita, Y.; Abe, Y.; Matsumoto, K.; Monda, K.; Hayase, S.; Kawatsura, M.; Itoh, T.
Preparation of Novel Hydrophobic Fluorine-substituted-alkyl Sulfate Ionic Liquids and Application as an Efficient Reaction Medium for Lipase-catalyzed Reaction
Tetrahedron Lett. 2006, 47, 1801-1804
26.Kawatsura, M.; Aburatani, S.; Uenishi, J.
Hafnium Trifluoromethanesulfonate [Hf(OTf)4] Catalyzed Conjugate Addition of Indoles to , -Enones
Synlett 2005, 2492-2494
25.Ikeda, D. ; Kawatsura, M.; Uenishi, J.
Palladium-Catalyzed Construction of Amino Acid Derivatives Possessing Vicinal Chiral Quaternary and Tertiary Carbon Centers at the α and β Positions.
Tetrahedron Lett. 2005, 46, 6663-6666
24.Hayashi, T.; Suzuka, T.; Okada, A.; Kawatsura, M.
Palladium-Catalyzed Asymmetric Allylic Substitution with an Indenide.
Tetrahedron Asymmetry 2004 15, 545-548
23.Utsunomiya, M.; Kawatsura, M.; Hartwig, J. F.
Palladium Catalyzed, Equilibrium Addition of Acidic OH bonds to Dienes
Angew. Chem. Int. Ed. 2003 5865-5868
22.Uenishi, J.; Kawatsura, M.; Ikeda, D.; Muraoka, N.
Construction of Consective Chiral Non-Racemic Quaternary and Tertiary Carbons: A Short Synthetic Route to (–)-Acetomycin.
Eur. J. Org. Chem. 2003, 3909-3912
21.Utsunomiya, M.; Kuwano, R.; Kawatsura, M.; Hartwig, J. F.
Rhodium-Catalyzed Anti-Markovnikov Hydroamination of Vinylarenes.
J. Am. Chem. Soc. 2003, 125, 5608-5609
20.Hayashi, T.; Okada, A.; Suzuka, T.; Kawatsura, M.
Highly Enantioselectivity in Rhodium-Catalyzed Allylic Alkylation of 1-Substituted 2-Propenyl Acetate
Org. Lett.. 2003, 5, 1713-1715
19.Suzuka, T.; Kawatsura, M.; Okada, A.; Hayashi, T.
Palladium-Catalyzed Asymmetric Allylic Substitution with a Cyclopentadinide. Asymmetric Synthesis of Metallocenes.
Tetrahedron Asymmetry 2003, 14, 511-515
18.Pawlas, J.; Nakao, Y.; Kawatsura, M.; Hartwig, J. F.
A General Nickel-Catalyzed Hydroamination of 1,3-Dienes by Alkylamines: Catalyst Selection, Scope and Mechanism
J. Am. Chem. Soc. 2002, 124, 3669-3679
17.Uozumi, Y.; Kawatsura, M.; Hayashi, T.
(R)-2-Diphenylphosphino-2’-methoy-1,1’-binaphthyl
Organic Syntheses 2001, 78, 1-13
16.Kawatsura, M.; Hartwig, J. F.
Transition Metal-Catalyzed Addition of Amines to Acrylic Acid Derivatives. A High-Throughput Method for Evaluating Hydroamination of Primary and Secondary Alkylamines
Organometallics 2001, 20, 1960-1964
15.Lober, O.; Kawatsura, M.; Hartwig, J. F.
Palladium-Catalyzed Hydroamination of 1,3-Dienes: A Colorimetric Assay and Enantioselective Additions
J. Am. Chem. Soc. 2001, 123, 4366-4367
14.Kawatsura, M.; Hartwig, J. F.
Palladium-Catalyzed Intermolecular Hydroamination of Vinylarenes Using Arylamines
J. Am. Chem. Soc. 2000, 122, 9546-9547
13.Kawatsura, M.; Uozumi, Y.; Ogasawara, M.; Hayashi, T.
Palladium-Catalyzed Asymmetric Reduction of Racemic Allylic Esters with Formic Acid: Effects of Phosphine Ligands on Isomerization of π-Allylpalladium Intermediates and Enantioselectivity
Tetrahedron 2000, 56, 2247-2257
12.Matsuda, F.; Kawatsura, M.; Hosaka, K.; Shirahama, H.
α- and β-Hydroxy Group Directed Stereoselective Ketone Olefin Couplings Mediated by SmI2
Chem. Eur. J. 1999, 5, 3252-3259
11.Matsuda, F.; Kawatsura, M.; Dekura, F.; Shirahama, H.
Urethane Group Directed Reductive Couplings Mediated by SmI2
J. Chem. Soc., Perkin Trans. 1 1999, 2371-2375
10.Hartwig, J. F.; Kawatsura, M.; Hauck, S. I.; Shaughnessy, K. H.; Alcazar-Roman, L.
Room Temperature Palladium-Catalyzed Amination of Aryl Halaides and Extended Scope of Aromatic C-N Bond Formation with a Commercial Ligand
J. Org. Chem. 1999, 64, 5575-5580
9.Kawatsura, M.; Hartwig, J. F.
Simple, Highly Active Palladium-Catalysts for Ketone and Malonate Arylation: Dissecting the Importance of Chelation and Steric Hindrance
J. Am. Chem. Soc. 1999, 121, 1473-1478
8.Hayashi, T.; Kawatsura, M.; Uozumi, Y.
Retention of Regiochemistry of Allylic Esters in Palladium-Catalyzed Allylic Alkylation in the Presence of a MOP Ligand
J. Am. Chem. Soc. 1998, 120, 1681-1687
7.Kawatsura, M.; Uozumi, Y.; Hayashi, T.
Regiocontrol in Palladium-Catalyzed Allylic Alkylation by Addition of Lithium Iodide
Chem. Commun. 1998, 217-218
6.Kawatsura, M.; Kishi, E.; Kito, M.; Sakai, T.; Shirahama, H.; Matsuda, F.
Hydroxy-Directed Stereocomplementary Pinacol Cyclizations Mediated by SmI2
Synlett 1997, 217-218
5.Hayashi, T.; Kawatsura, M.; Uozumi, Y.
Regio- and Enantio-Selective Allylic Alkylation Catalysed by a Chiral Monophosphine-Palladium Complex
Chem. Commun. 1997, 561-562
4.Hayashi, T.; Kawatsura, M.; Iwamura, H.; Yamaura, Y.; Uozumi, Y.
Catalytic Asymmetric Synthesis of Optically Active Alkenes by Palladium-Catalysed Asymmetric Reduction of Racemic Allylic Esters with Formic Acid
Chem. Commun. 1996, 1767-1768
3.Kawatsura, M.; Dekura, F.; Shirahama, H.; Matsuda, F.
Samarium (II) Iodide Mediated Intermolecular Ketone-Olefin Couplings Chelation-Controlled by (Alkoxycarbonyl)amino Groups
Synlett 1996, 373-376
2.Kawatsura, M.; Hosaka, K.; Matsuda, F.; Shirahama, H.
Samarium (II) Iodide Mediated Intermolecular Ketone-Olefin Couplings Chelation- Controlled by β-Hydroxy Groups
Synlett 1995, 729-732
1.Kawatsura, M.; Matsuda, F.; Shirahama, H.
Samarium (II) Iodide Promoted Intermolecular Ketone-Olefin Couplings Chelation-Controlled by α-Hydroxy Groups
J. Org. Chem. 1994, 59, 6900-6901
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