79. Palladium-Catalyzed Decarbonylative Cross-Coupling of Azinecarboxylates with Arylboronic Acids
 2016-09-19_16-05-36 2016-10-01_14-25-20

Muto, K.; Hatakeyama, T.; Itami, K.; Yamaguchi, J.
Org. Lett. 201618, 5106–5109.
DOI 10.1021/acs.orglett.6b02556
Detail Palladium-Catalyzed Decarbonylative Cross-Coupling

78. C-H Activation Enables Rapid Structure-Activity Relationship Study of Arylcylclopropyl amines for Potent and Selective LSD1 Inhibitors
2016-09-19_18-20-06 2016-08-14_11-22-47

Miyamura, S.; Araki, M;; Ota, Y; Itoh, Y; Yasuda, S; Masada, M; Taniguchi, T;  Sowa, Y; Sakai, T; Suzuki, T; Itami, K.; Yamaguchi, J.
Org. Biomol. Chem.  2016, 14, 8576–8585.
DOI 10.1039/C6OB01483F
Detail C-H Activation Enables Rapid SAR for LSD1 Inhibitors

77. Cyanation of Phenol Derivatives with Aminoacetonitriles by Nickel Catalysis
2016-09-19_16-05-36 ol-2016-02265d_0014

Takise, R.; Itami, K.; Yamaguchi J.
Org. Lett. 2016, 18, 4428–4431.
DOI 10.1021/acs.orglett.6b02265
Detail Cyanization of phenol derivatives with metal-free cyanating agents

76. Nickel-Catalyzed Aromatic C–H Functionalization
2016-08-03_15-09-39 2016-08-03_15-13-21-575x380

Yamaguchi, J*; Muto, K.; Itami, K.

Top Curr. Chem, 2016,  374, 55.

DOI 10.1007/s41061-016-0053-z
Detail Nickel-Catalyzed Aromatic C–H Functionalization

75. The AMOR Arabinogalactan Sugar Chain Induces Pollen-Tube Competency to Respond to Ovular Guidance
2016-09-19_18-17-37 2016-04-09_00-04-40

Mizukami, A. G.; Inatsugi, R.; Jiao, J.; Kotake, T.l Kuwata, K.; Ootani, K.; Okuda, S.; Sankaranarayanan, S.; Sato, Y.; Maruyama, D.; Iwai, H.; Garénaux, E.; Sato, C.; Kitajima, K.; Tsumuraya, Y.; Mori, H.; Yamaguchi, J.;  Itami, K.; Sasaki, N.; Higashiyama, T.
Current. Biology 2016, 26, 1091–1097.
DOI 10.1016/j.cub.2016.02.040

74. Development and Elucidation of the Ni-Catalyzed Direct Coupling Reaction
2016-09-19_18-15-33 2016-04-02_15-33-20-575x370

Yamaguchi, J.*; Muto, K.; Itami, K.
Chemical Times, 2016, 1–7.
Link  Link
Detail Development and Elucidation of the Ni-Catalyzed Direct Coupling Reaction

73. Synthesis of Triarylpyridines in Thiopeptide Antibiotics by Using a C−H Arylation/Ring-Transformation Strategy
2016-09-19_18-13-40 2016-02-26_17-56-38

Amaike, K.; Itami, K.; Yamaguchi, J.
Chem. Eur. J. 2016, 22, 4384–4388.
DOI 10.1002/chem.201600351
Detail Making Triarylpyridines

72. Microwave-assisted regioselective direct C–H arylation of thiazole derivatives leading to increased σ1 receptor affinity
2016-09-19_18-12-46 GA

Kokornaczyk, A.; Schepmann, D.; Yamaguchi, J.; Itami, K.; Wünsch, B.
Med. Chem. Commun. 2016, 7, 327.
DOI 10.1039/C5MD00526D

71. Synthesis of Natural Products and Pharmaceuticals via Catalytic C–H Functionalization
2016-09-19_18-11-54 2016-03-22_02-59-20-3-575x380

Yamaguchi, J.; Amaike, K.; Itami, K.
“Transition Metal-Catalyzed Heterocycle Synthesis via C-H Activation”、2016, Wiley-VCH
DOI 10.1002/9783527691920.ch16
Detail Synthesis of Natural Products and Pharmaceuticals via Catalytic C–H Functionalization

Return Top