English
(188) All-benzene Carbon Nanocages: Size-selective Synthesis, Photophysical Properties, and Crystal Structure
Katsuma Matsui, Yasutomo Segawa, and Kenichiro Itami
J. Am. Chem. Soc. 2014, 136, 16452-16458. DOI: 10.1021/ja509880v 【detail】
(187) Key Mechanistic Features of Ni-catalyzed C–H/C–O Biaryl Coupling of Azoles and Naphthalen-2-yl Pivalates
Huiying Xu, Kei Muto, Junichiro Yamaguchi, Cunyuan Zhao, Djamaladdin G Musaev, and Kenichiro Itami
J. Am. Chem. Soc. 2014, 136, 14834. DOI: 10.1021/ja5071174
(186) β-Selective C–H Arylation of Pyrroles Leading to Concise Syntheses of Lamellarins C and I
Kirika Ueda , Kazuma Amaike , Richard M. Maceiczyk , Kenichiro Itami , and Junichiro Yamaguchi
J. Am. Chem. Soc. 2014, 136, 13226. DOI: 10.1021/ja508449y 【detail】
(185) Branch-Selective Allylic C–H Carboxylation of Terminal Alkenes by Pd/sox Catalyst
Hiroki Kondo, Feng Yu, Junichiro Yamaguchi, Guosheng Liu, and Kenichiro Itami
Org. Lett. 2014, 16, 4212. DOI: 10.1021/ol5019135 【detail】
(184) Nickel-Catalyzed α-Arylation of Ketones with Phenol Derivatives
Ryosuke Takise, Kei Muto, Junichiro Yamaguchi and Kenichiro Itami
Angew. Chem. Int. Ed. 2014, 53, 6791. DOI: 10.1002/anie.201403823
Highlighted in Newspapers (Chemical Daily News, Kagaku Shinbun), Chemistry Views, Chemistry Processing
(183) 2,4- and 2,5-Disubstituted Arylthiazoles: Rapid Synthesis by C–H Coupling and Biological Evaluation
Lilia Lohrey, Takahiro N. Uehara, Satoshi Tani, Junichiro Yamaguchi, Hans-Ulrich Humpf and Kenichiro Itami
Eur. J. Org. Chem. 2014, 3387. DOI: 10.1002/ejoc.201402129 【detail】
(182) Synthesis and Dimerization of Chloro[10]cycloparaphenylene: A Directly Connected Cycloparaphenylene Dimer
Yuuki Ishii, Sanae Matsuura, Yasutomo Segawa, and Kenichiro Itami
Org. Lett. 2014, 16, 2174. DOI: 10.1021/ol500643c 【detail】
(181) Excitation Recombination Dynamics in Nanoring Cycloparaphenylenes
Taishi Nishihara, Yasutomo Segawa, Kenichiro Itami, and Yoshihiko Kanemitsu
Chem. Sci. 2014, 5, 2293, DOI: 10.1039/c3sc53462f 【detail】
(180) Manganese-Catalyzed Intermolecular C–H/C–H Coupling of Carbonyls and Heteroarenes
Keika Hattori, Asraa Ziadi, Kenichiro Itami, and Junichiro Yamaguchi
Chem. Commun. 2014, 50, 4105. DOI:10.1039/C4CC01376J 【detail】
Most Read Article (March, 2014)
(179) Late-Stage C–H Coupling Enables Rapid Identification of HDAC Inhibitors: Synthesis and Evaluation of NCH-31 Analogues
Hiromi Sekizawa, Kazuma Amaike, Yukihiro Itoh, Takayoshi Suzuki, Kenichiro Itami, and Junichiro Yamaguchi
ACS. Med. Chem. Lett. 2014, 5, 582. DOI: 10.1021/ml500024s 【detail】
Most Read Article (March, 2014)
(178) Size-Selective Complexation and Extraction of Endohedral Metallofullerenes with Cycloparaphenylene
Yusuke Nakanishi, Haruka Omachi, Sanae Matsuura, Yasumitsu Miyata, Ryo Kitaura, Yasutomo Segawa, Kenichiro Itami and Hisanori Shinohara
Angew. Chem. Int. Ed. 2014, 53, 3102-3106. DOI: 10.1002/anie.201311268 【detail】
(177) Cross-Dehydrogenative-Coupling Reactions without Metals
Hideto Ito, Kirika Ueda, and Kenichiro Itami
From C-H to C-C Bonds : Cross-Dehydrogenative-Coupling (Eds: Chao-Jun Li, DOI: 10.1039/9781782620082), Chapter 8,
Royal Society of Chemistry, 2015, 153–196. DOI: 10.1039/9781782620082-00153.
(176) Tris(1,1,1,3,3,3-hexafluoro-2-propyl)phosphite
Kirika Ueda and Kenichiro Itami
Electronic Encyclopedia of Reagents for Organic Synthesis, Wiley, online.
(175) Synthesis and Properties of Cycloparaphenylene-2,7-pyrenylene: A Pyrene-Containing Carbon Nanoring
Akiko Yagi, Gandikota Venkataramana, Yasutomo Segawa, and Kenichiro Itami
Chem. Commun. 2014, 50, 957-959. doi: 10.1039/C3CC48198K 【detail】
(174) Selective Synthesis of [7]- and [8]Cycloparaphenylenes
Friederike Sibbel, Katsuma Matsui, Yasutomo Segawa, Armido Studer and Kenichiro Itami
Chem. Commun. 2014, 50, 954-956. doi: 10.1039/C3CC48683D 【detail】
(173) Synthesis of Dihydrobenzo[b]furans by Diastereoselective Acyloxyarylation
Kazuhiro Hata, Zhiheng He, Constantin Gabriel Daniliuc, Kenichiro Itami, and Armido Studer
Chem. Commun., 2014, 50, 463-465. DOI: 10.1039/C3CC47350C 【detail】
(172) Diverse Modification of the 4-Methylphenyl Moiety of TAK-779 by Late-Stage Suzuki-Miyaura Cross-Coupling
Anna Junker, Dirk Schepmann, Junichiro Yamaguchi, Kenichiro Itami, Andreas Faust, Klaus Kopka, Stefan Wagner, Bernhard Wünsch
Org. Biomol. Chem. 2014, 12, 177-186. DOI: 10.1039/C3OB41873A
(171) Programmed Synthesis of Arylthiazoles through Sequential C-H Couplings
Satoshi Tani, Takahiro N. Uehara, Junichiro Yamaguchi and Kenichiro Itami,
Chem. Sci. 2014, 5, 123-125. DOI: 10.1039/C3SC52199K 【detail】
Most Read Article (October, 2013), Higlighted in Synfacts