2014

2014

(188) All-benzene Carbon Nanocages: Size-selective Synthesis, Photophysical Properties, and Crystal Structure

Katsuma Matsui, Yasutomo Segawa, and Kenichiro Itami

J. Am. Chem. Soc. 2014136, 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. Lett201416, 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. Ed201453, 6791. DOI: 10.1002/anie.201403823

Highlighted in Newspapers (Chemical Daily News, Kagaku Shinbun), Chemistry ViewsChemistry 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. Lett20145, 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. 201453, 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. 201412, 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

 

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