2017(13)

92. Catalytic α-Arylation of Ketones with Heteroaromatic Esters

Isshiki, R.; Takise, R.; Itami, K.; Muto, K.; Yamaguchi, J.
Synlett 2017, 28, 2599–2603.(Invited contribution)
DOI10.1055/s-0036-1589120
Detail ヘテロ芳香環エステルとケトンのα-アリール化反応

91. Synthesis of Octaaryl Naphthalenes and Anthracenes with Different Substituents

Suzuki, S.; Itami, K.; Yamaguchi, J.
Angew. Chem., Int. Ed. 2017, 56, 15010-15013.
DOI10.1002/anie.201709332
Detail Yamatano Orochi: Octaaryl Naphthalenes and Anthracenes

90. Cross-coupling of Aromatic Esters and Amides

Takise, R.; Muto, K.; Yamaguchi, J.
Chem. Soc. Rev  2017,46, 5864-5888.
DOI10.1039/C7CS00182G 
Highlights Highlighted as an Inside back Cover
Detail Cross-coupling of aromatic esters and amides

89. Thiazole-based sigma-1 receptor ligands: Diversity by late-stage C-H arylation of thiazoles, structure affinity and selectivity relationships and molecular interactions

Kokornaczyk, A.; Schepmann, D.; Yamaguchi, J.; Itami, K.; Laurini, E.; Fermeglia, M.; Pricl, S.; Wünsch, B
ChemMedChem 2017, 12, 1070–1080.
DOI 10.1002/cmdc.201700166

88.Theoretical Elucidation of Potential Enantioselectivity in a Pd-Catalyzed Aromatic C-H Coupling Reaction

Nishimoto,Y.; Kondo, H.; Yamaguchi, K.; Yokogawa, D.; Yamaguchi, J.; Itami, K.; Irle, S.; 
J. Org. Chem. 2017, 82, 4900–4906.
DOI 10.1021/acs.joc.6b02675

87. Synthesis of Multiply Arylated Pyridines

Asako, T.; Hayashi, W.; Suzuki, S.; Amaike, K.; Itami, K.; Muto, K.; Yamaguchi, J.
Tetrahedron 2017, 73, 3669-3676 (Invited contribution).
DOI 10.1016/j.tet.2017.03.095
Detail Synthesis of Multiply Arylated Pyridines

86. Rh-Catalyzed Regiodivergent Hydrosilylation of Acyl aminocyclopropanes Controlled by Monophosphine Ligands

Kondo, H.: Itami, K.; Yamaguchi, J.
Chem Sci. 2017, 8, 3799–3803.
DOI 10.1039/C7SC00071E
Detail Rh-Catalyzed Regiodivergent Hydrosilylation of Acyl aminocyclopropanes Controlled by Monophosphine Ligands

85. Decarbonylative Diaryl Ether Synthesis by Pd and Ni Catalysis

Takise, R.; Isshiki, R. Muto K.; Itami, K.; Yamaguchi, J.
J. Am. Chem. Soc. 2017, 139, 3340–3343.
DOI 10.1021/jacs.7b00049
Highlights 化学工業日報 日経産業新聞 Phys.org  c2W ScienceDaily  Chem-Station
Highlights Most Read Article (March, 2017)
Detail Decarbonylative Diaryl Ether Synthesis by Pd and Ni Catalysis

84. Synthesis of Fully Arylated (Hetero)arenes

Suzuki, S.; Yamaguchi. J.
Chem. Commun. 2017, 53, 1568–1582. (Invited contribution)
DOI 10.1039/C6CC09550J
Detail Synthesis of Fully Arylated (Hetero)arenes

83. Structure-Activity Relation of AMOR Sugar Molecule thatActivates Pollen-Tubes for Ovular Guidance



 2016-12-04_21-48-47

Jiao J.; Mizukami, A.G.; Sankaranarayanan, S.; Yamaguchi, J.; Itami, K.; Higashiyama, T.
Plant Physiol. 2017, 173, 354–363.
DOI 10.1104/pp.16.01655

82. Toward an Ideal Synthesis of (Bio)molecules through Direct Arene Assembling Reactions
 
2016-11-28_20-40-55
 2016-11-28_18-24-24

Yamaguchi, J.; Itami, K
Bull. Chem. Soc. Jpn. 2017, 90, 367–383 (Award accounts). 
DOI 10.1246/bcsj.20160365
Highlights Most Read Article (December, 2016)
Highlights Highlighted as a Back Cover
Detail Direct Arene Assembling Reactions

81. Palladium-Catalyzed Decarbonylative Alkynylation of Aromatic Esters
 2016-09-19_16-50-07 cl-161001figc

Okita, T.; Kumazawa, K.; Takise, R.; Muto, K.; Itami, K.; Yamaguchi, J.
Chem Lett. 2017, 46, 218–220.
DOI 10.1246/cl.161001
Highlights Most Read Article (November–December, 2016)
Detail Decarbonylative Alkynylation

80. Syntheses of Biologically Active 2-Arylcyclopropylamines
 
  

Miyamura, S.; Itami, K.; Yamaguchi, J
Synthesis, 2017, 49, 1131–1149.
DOI 10.1055/s-0036-1588390
Highlights Highlighted as a Front Cover
Detail　Syntheses of Biologically Active ACPAs

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