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Publications-Junichiro Yamaguchi-

【発表論文】

[60] Decarbonylative organoboron cross-coupling of esters by nickel catalysis

Kei Muto, Junichiro Yamaguchi, Djamaladdin G. Musaev and Kenichiro Itami

Nature. Commun. 20156, 7508. DOI: 10.1038/ncomms8508

[59] C-H Activation Generates Period-Shortening Molecules That Target Cryptochrome in the Mammalian Circadian Clock

Tsuyoshi Oshima, Iori Yamanaka, Anupriya Kumar, Junichiro Yamaguchi, Taeko Nishiwaki-Ohkawa, Kei Muto, Rika Kawamura, Tsuyoshi Hirota,  Kazuhiro Yagita,  Stephan Irle, Steve A. Kay, Takashi Yoshimura and Kenichiro Itami

Angew. Chem., Int. Ed201554, 7193-7197. DOI: 10.1002/anie.201502942 【detail

Highlighted in News Paper (Chu-nichi Shinbun)

[58] Synthesis and characterization of hexaarylbenzenes with five or six different substituents enabled by programmed synthesis

Shin Suzuki, Yasutomo Segawa, Kenichiro Itami and Junichiro Yamaguchi

Nature Chem2015, 7, 227-233. DOI:10.1038/nchem.2174 【detail

[57] Concise Syntheses of Dictyodendrins A and F by a Sequential C–H Functionalization Strategy

Atsushi D. Yamaguchi, Kathryn M. Chepiga, Junichiro Yamaguchi, Kenichiro Itami, and Huw M. L. Davies,

J. Am. Chem. Soc. 2015, ASAP. DOI: 10.1021/ja512059d 【detail

[56] Synthesis, binding affinity and structure–activity relationships of novel, selective and dual targeting CCR2 and CCR5 receptor antagonists

Anna Junker, Artur K. Kokornaczyk, Annelien J. M. Zweemer, Bastian Frehland, Dirk Schepmann, Junichiro Yamaguchi, Kenichiro Itami, Andreas Faust, Sven Hermann, Stefan Wagner, Michael Schäfers,  Michael Koch, Christina Weiss, Laura H. Heitman, Klaus Kopkai and   Bernhard Wünsch

Org. Biomol. Chem.2015, Advance Article DOI: 10.1039/C4OB02397H

[55] Ni-Catalyzed α-Arylation of Esters and Amides with Phenol Derivatives

Eva Koch, Ryosuke Takise, Armido Studer, Junichiro Yamaguchi and Kenichiro Itami

Chem. Commun.201551, 855.  DOI: 10.1039/C4CC08426Hdetail

[54]  Stereodivergent Synthesis of Arylcyclopropylamines by Sequential C–H Borylation and Suzuki–Miyaura Coupling

Shin Miyamura, Misaho Araki, Takayoshi Suzuki, Junichiro Yamaguchi, and Kenichiro Itami

Angew. Chem. Int. Ed. 2015, 54, 846. DOI: 10.1002/anie.201409186

[53]  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. 2014136, 14834. DOI: 10.1021/ja5071174

[52] 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

Most Read Article (September, 2014) 

[51]  Regioselective Allylic C–H Oxidation of Terminal Alkenes with Pd/sulfoxide-oxazoline Catalyst

Hiroki Kondo, Feng Yu, Junichiro Yamaguchi, Guosheng Liu, and Kenichiro Itami

Org. Lett201416, 4212. DOI: 10.1021/ol5019135 【detail

[50] Nickel-Catalyzed α-Arylation of Ketones with Phenol Derivatives

Ryosuke Takise, Kei Muto, Junichiro Yamaguchi and Kenichiro Itami

Angew. Chem. Int. Ed2014, 53, 6791. DOI: 10.1002/anie.201403823

[49] 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

[48]  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) 

[47] 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. Lett2014, 582. DOI: 10.1021/ml500024s 【detail

Most Read Article (March, 2014) 

[46]  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

[45] 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 Articles in October in 2013, Highlighted in Synfacts

[44]  Isolation, Structure, and Reactivity of an Arylnickel(II) Pivalate Complex in Catalytic C-H/C-O Biaryl Coupling

Kei Muto, Junichiro Yamaguchi, Aiwen Lei, and Kenichiro Itami

J. Am. Chem. Soc. 2013, 135, 16384–16387. DOI: 10.1021/ja409803xdetail

[43] Palladium-Catalyzed C–H and C–N Arylation of Aminothiazoles with Arylboronic Acids

Takahiro N. Uehara, Junichiro Yamaguchi, Kenichiro Itami

Asian J. Org. Chem. 20132, 938-942. DOI: 10.1002/ajoc.201300172 【detail

(Dedicated to Professor Teruaki Mukaiyama on the occasion of the 40th anniversary of the Mukaiyama aldol reaction)

Highlighted in Chemistry Views Highlighted in Synfacts.

[42]  C–H Alkenylation of Azoles with Enols and Esters by Nickel Catalysis

Lingkui Meng, Yuko Kamada, Kei Muto, Junichiro Yamaguchi, and Kenichiro Itami

Angew. Chem. Int. Ed. 2013, 52, 10048 DOI: 10.1002/anie.201304492 【detail

[41] Aromatic C–H Coupling with Hindered Arylboronic Acids by Pd/Fe Dual Catalysts

Kazuya Yamaguchi, Hiroki Kondo, Junichiro Yamaguchi, and Kenichiro Itami

Chem. Sci. 2013, 4, 3753-3757. DOI: 10.1039/C3SC51206A 【detail

Most Read Articles in June in 2013

[40] Synthesis of Thiophene-Based TAK-779 Analogues by C–H Arylation

Anna Junker, Junichiro Yamaguchi, Kenichiro Itami, and Bernhard Wünsch

J. Org. Chem. 201378, 5579–5586. DOI: 10.1021/jo400692p 【detail

[39] Nickel-Catalyzed Direct Coupling of Heteroarenes

Junichiro Yamaguchi, Kei Muto, Kazuma Amaike, Takuya Yamamoto, and Kenichiro Itami

J. Synth. Org. Chem. Jpn. 201371, 576–583.

[38] Improvement of σ1 receptor affinity by late-stage C–H bond arylation of spiro cyclic lactones

Christina Meyer, Benedikt Neue, Dirk Schepmann, Shuichi Yanagisawa, Junichiro Yamaguchi, Ernst-Ulrich Würthwein, Kenichiro Itami, Bernhard Wünsch,

Bioorg. Med. Chem.  2013, 21, 1844.

DOI: 10.1016/j.bmc.2013.01.038

[37]  Pd-catalyzed direct C-H bond functionalization of spirocyclic sigma-1 ligands: generation of a pharmacophore model and analysis of reverse binding mode by docking into a 3D homology model of the sigma-1 receptor

Christina Meyer, Dirk Schepmann, Shuichi Yanagisawa, Junichiro Yamaguchi, Valentina Dal Col, Erik Laurini, Kenichiro Itami, Sabrina Pricl, and Bernhard Wünsch

J. Med. Chem. 201255, 8047.

DOI: 10.1021/jm300894h 【detail

[36] Decarbonylative C–H Coupling of Azoles and Aryl Esters: Unprecedented Nickel Catalysis and Application to the Synthesis of Muscoride A

Kazuma Amaike, Kei Muto, Junichiro Yamaguchi, and Kenichiro Itami,

J. Am. Chem. Soc. 2012134, 13573–13576.

DOI: 10.1021/ja306062c 【detail

Highlighted in Newspapers (Chu-nichiAsahi, The Chemical Daily, Yahoo!News, Mynavi-News, Nikkan kogyo, Kagaku Shinbun)

Most Read Articles in August 2012

[35] Late-Stage C–H Bond Arylation of Spirocyclic sigma-1 Ligands for Analysis of Complementary sigma-1 Receptor Surface

Christina Meyer, Dirk Schepmann, Shuichi Yanagisawa, Junichiro Yamaguchi, Bernhard Wünsch, and Kenichiro Itami

Eur. J. Org. Chem. 2012, 5972–5979.

DOI: 10.1002/ejoc.201200837 【detail

[34] Pd- and Cu-catalyzed C–H Arylation of Indazoles

Keika Hattori, Kazuya Yamaguchi, and Kenichiro Itami

Tetrahedron (Special Issue)201268, 7605-7612.

DOI: 10.1016/j.tet.2012.05.091 【detail

[33]  Hindered Biaryls by C-H Coupling: Bisoxazoline-Pd Catalysis Leading to Enantioselective C-H Coupling

Kazuya Yamaguchi, Junichiro Yamaguchi, Armido Studer, and Kenichiro Itami

Chem. Sci, 2012, 7, 1256.

DOI:10.1039/C2SC20277Hdetails

Highlighted RSC Chemical Science blog, Most Read Articles in March and April 2012

[32] Mechanistic Studies on the Pd-catalyzed Direct C¿H Arylation of 2-Substituted Thiophene Derivatives with Arylpalladium Bipyridyl Complexes

Marc Steinmetz, Kirika Ueda, Stefan Grimme, Junichiro Yamaguchi, Sylvia Kirchberg, Kenichiro Itami, Armido Studer,

Chem. Asian J. 2012, 7, 1256–1260.

DOI: 10.1002/asia.201101011 【detail

[31] Nickel-Catalyzed C−H/C−O Coupling of Azoles with Phenol Derivatives

Kei Muto, Junichiro Yamaguchi, Kenichiro Itami,

J. Am. Chem. Soc. 2012134, 169-172.

DOI: 10.1021/ja210249h 【details

Highlighted in Newspapers (YomiuriChu-nichiThe Chemical DailyYahoo!News, NanotechJapan Nikkan kogyoKagaku Shinbun), Most Read Articles (January, 2012), Highlighted as a “SynStory” article in SYNFORM (April 2012), Highlighted in Chemical Engineering (Feb 2012) 

[30] Synthesis of Dragmacidin D via Direct C-H Couplings

Debashis Mandal, Atsushi D. Yamaguchi,  Junichiro Yamaguchi,  Kenichiro Itami, J. Am. Chem. Soc. 2011133, 19660–19663.

DOI: 10.1021/ja209945x 【details

Most Read Articles (November 2011), Highlighted in Chemistry World  

[29] Exploitation of an additional hydrophobic pocket of σ1 receptors: Late-stage diverse modifications of spirocyclic thiophenes by C–H bond functionalization

C. Meyer, B. Neue, D. Schepmann, S. Yanagisawa, J. Yamaguchi, E.-U. Würthwein, K. Itami, B. Wünsch, Org. Biomol. Chem2011, 9, 8016.

DOI: 10.1039/C1OB06149F

[28] Enantioselective Total Syntheses of (−)-Palau’amine, (−)-Axinellamines, and (−)-Massadines

I. B. Seiple, S. Su, I. S. Young, A. Nakamura, J. Yamaguchi, L. Jørgensen, R. A. Rodriguez, D. P. O’Malley, T. Gaich, M. Kck, and P. S. Baran, J. Am. Chem. Soc. 2011, 133, 14710.

DOI: 10.1021/ja2047232

Most Read Articles (October 2011)

[27] Nickel-Catalyzed C–H Arylation of Azoles with Haloarenes: Scope, Mechanism, and Applications to the Synthesis of Bioactive Molecules

T. Yamamoto, K. Muto, M. Komiyama, J. Canivet, J. Yamaguchi, and K. Itami Chem. Eur. J. 2011, 17, 10113.

DOI: 10.1002/chem.201101091. 【details

Highlighted in SYNFACTS

[26] Oxidative C–H/C–H Coupling of Azine and Indole/Pyrrole Nuclei: Palladium Catalysis and Synthesis of Eudistomin U

A. D. Yamaguchi, D. Mandal, J. Yamaguchi, and K. Itami, Chem. Lett. 2011, 40, 555 -557.

DOI: 10.1246/cl.2011.555 details

Selected as “Editor’s Choice” Most-Accessed Articles, Highlighted in Angew. Chem. Int. Ed.

[25] Oxidative Biaryl Coupling of Thiophenes and Thiazoles with Arylboronic Acids through Palladium Catalysis: Otherwise-Difficult C4-Selective C-H Arylation Enabled by Boronic Acids

S. Kirchberg, S. Tani, K. Ueda, J. Yamaguchi, A. Studer, and K. Itami, Angew. Chem. Int. Ed. 2011, 50, 2387.

DOI: 10.1002/anie.201007232details

Highlighted in SYNFACTS

[24] A General Catalyst for the β-Selective C-H Bond Arylation of Thiophenes with Iodoarenes

K. Ueda, S. Yanagisawa, J. Yamaguchi, K. Itami, Angew. Chem. Int. Ed. 2010, 49, 8946.

DOI; 10.1002/anie.201005082details

Highlighted in SYNFACTS

[23] Total Synthesis of Palau’amine

I. B. Seiple, S. Su, I. S. Young , C. A. Lewis , J Yamaguchi,  P. S. Baran Angew. Chem. Int. Ed. 2010, 49, 1095.

DOI: 10.1002/anie.200907112

Selected as VIP paper and Cover Picture in Angew. Chem. Int. Ed.

Highlighted in Nature, C&EN, Wired Science,Sciencedaily, R&D, Health Candal.com, Chemistry World Blog(RSC), Tot. Syn. Dot Com, Chem-Station, C2W – C2W

Financial Express, Angew. Chem., Gendai-Kagaku

Most-Accessed Articles (January 2010, 6/2009~7/2010)

[22]Fe-Catalyzed Oxidative Coupling of Heteroarenes and Methylamines
M. Ohta, M. P. Quick, J. Yamaguchi, B. Wünsch, and K. Itami Chem. Asian J. 2009, 4, 1416.

DOI:10.1002/asia.200900157details
Most-Accessed Articles (July 2009)

[21] Nickel-Catalyzed Biaryl Coupling of Heteroarenes and Aryl Halides/Triflates

J. Canivet, J. Yamaguchi, I. Ban, K. Itami, Org. Lett., 2009, 11, 1733. 【details

DOI: 10.1021/ol9001587

Highlighted in SYNFACTS

Top 20 Most Cited Articles 2009-2011
[20] The Asymmetric Total Synthesis of (+)-Cytotrienin A, an Ansamycin-Type Anticancer Drug
Y. Hayashi, M. Shoji, H. Ishikawa, J. Yamaguchi, T. Tamura, H. Imai, Y. Nishigaya, K. Takabe, H. Kakeya, H. Osada, Angew. Chem. Int. Ed., 2008, 47, 6657.

DOI: 10.1002/anie.200802079
Highlighted in SYNFACTS

[19] Total Synthesis of (±)-Axinellamines A and B
D. P. O’Malley, J. Yamaguchi, I. S. Young, I. B. Seiple, P. S. Baran, Angew. Chem. Int. Ed., 2008, 47, 3581.

DOI: 10.1002/anie.200801138
Selected as VIP paper and Inside Cover in Angew. Chem. Int. Ed.
Highlighted in Tot. Syn. Dot Com

[18] Synthesis of 1,9-Dideoxy-pre-axinellamine
J. Yamaguchi, I. B. Seiple, I. S. Young, D. P. O’Malley, M. Maue, P. S. Baran, Angew. Chem. Int. Ed., 2008, 47, 3578.

DOI: 10.1002/anie.200705913
[17] Direct Asymmetric a-Amination of Cyclic Ketones Catalyzed by Siloxyproline
Y. Hayashi, S. Aratake, Y. Imai, K. Hibino, Q. -Y. Chen, J. Yamaguchi, T. Uchimaru, Chem. Asian J., 2008, 3, 225.

DOI: 10.1002/asia.200700307
[16] Organocatalyst-Mediated Enantioselective Intramolecular Aldol Reaction Featuring the Rare Combination of Aldehyde as Nucleophile and Ketone as Electrophile
Y. Hayashi, H. Sekizawa, J. Yamaguchi, H. Gotoh, J. Org. Chem., 2007, 72, 6493.

DOI: 10.1021/jo0709100
[15]Total Synthesis of Marinomycins A-C and of Their Monomeric Counterparts Monomarinomycin A and iso-Monomarinomycin A
K. C. Nicolaou, A. L. Nold, R. R. Milburn, C. S. Schindler, K. P. Cole, J. Yamaguchi, J. Am. Chem. Soc., 2007, 129, 1760.

DOI: 10.1021/ja068053p
[14] Enantio- and Diastereoselective Total Synthesis of (+)-Panepophenanthrin, a Ubiquitin-Activating Enzyme Inhibitor, and Biological Properties of Its New Derivatives
M. Matsuzawa, H. Kakeya, J. Yamaguchi, M. Shoji, R. Onose, H. Osada, Y. Hayashi, Chem. Asian J., 2006, 1, 845.

DOI: 10.1002/asia.200600199
[13] Large Nonlinear Effect Observed in the Enantiomeric Excess of Proline in Solution and That in the Solid State
Y. Hayashi, M. Matsuzawa, J. Yamaguchi, S. Yonehara, Y. Matsumoto, M. Shoji, D. Hashizume, H. Koshino, Angew. Chem. Int. Ed., 2006, 45, 4593.

DOI: 10.1002/anie.200601506
[12] Concise Enantio- and Diastereoselective Total Syntheses of Fumagillol, RK-805, FR65814, Ovalicin, and 5-Demethylovalicin
J. Yamaguchi, M. Toyoshima, M. Shoji, H. Kakeya, H. Osada, Y. Hayashi, Angew. Chem. Int. Ed., 2006, 45, 789.

DOI: 10.1002/anie.200502826
[11] Determination by Asymmetric Total Synthesis of The Absolute Configuration of Lucilactaene, a Cell Cycle Inhibitor in p53-Transfected Cells
J. Yamaguchi, H. Kakeya, T. Uno, M. Shoji, H. Osada, Y. Hayashi, Angew. Chem. Int. Ed., 2005, 44, 3110.

DOI: 10.1002/anie.200500060
[10] A Highly Active 4-Siloxyproline Catalyst for Asymmetric Synthesis
Y. Hayashi, J. Yamaguchi, K. Hibino, T. Sumiya, T. Urushima, M. Shoji, D. Hashizume, H. Koshino, Adv. Synth. Catal., 2004, 346, 1435.

DOI: 10.1002/adsc.200404166
Highlighted in Letters in Organic Chemistry, 2005, 2, 5 , 392-397 (News and Views).
[9] Structure-Activity Relationships of Epolactaene Derivatives: Structural Requirements for Inhibition of Hsp60 Chaperone Activity
Y. Nagumo, H. Kakeya, J. Yamaguchi, T. Uno, M. Shoji, Y. Hayashi, H. Osada, Bioorg. Med. Chem. Lett., 2004, 14, 4425.

DOI: 10.1016/j.bmcl.2004.06.054
[8] Direct Proline-Catalyzed Asymmetric a-Aminoxylation of Aldehydes and Ketones
Y. Hayashi, J. Yamaguchi, T. Sumiya, K. Hibino, M. Shoji, J. Org. Chem., 2004, 69, 5966-5973.

DOI: 10.1021/jo049338s
[7] Direct Proline-Catalyzed Asymmetric a-Aminoxylation of Ketones
Y. Hayashi, J. Yamaguchi, T. Sumiya, M. Shoji, Angew. Chem. Int Ed., 2004, 43, 1112.

DOI: 10.1002/ange.200353085
Selected as VIP paper in Angew. Chem. Int. Ed.
[6] Direct Proline Catalyzed Asymmetric a-Aminooxylation of Aldehydes
Y. Hayashi, J. Yamaguchi, K. Hibino, M. Shoji, Tetrahedron Lett., 2003, 44, 8293.

DOI: 10.1016/j.tetlet.2003.09.057
[5] Asymmetric Total Synthesis of Pseurotin A
Y. Hayashi, M. Shoji, S. Yamaguchi, T. Mukaiyama, J. Yamaguchi, H. Kakeya, H. Osada, Org. Lett., 2003, 5, 2287.

DOI:10.1021/ol034630s
[4] Asymmetric Total Synthesis of (-)-Azaspirene, a Novel Angiogenesis Inhibitor
Y. Hayashi, M. Shoji, J. Yamaguchi, K. Sato, S. Yamaguchi, T. Mukaiyama, K. Sakai, Y. Asami, H. Kakeya, H. Osada, J. Am. Chem. Soc., 2002, 124, 12078.

DOI: 10.1021/ja0276826
[3] The Diastereoelective Asymmetric Total Synthesis of NG-391, a Neuronal Cell-Protecting Molecule
Y. Hayashi, J. Yamaguchi, M. Shoji, Tetrahedron, 2002, 58, 9839.

DOI: 10.1016/S0040-4020(02)01290-5
[2] Diastereoselective Total Synthesis of Both Enantiomers of Epolactaene
Y. Hayashi, J. Kanayama, J. Yamaguchi, M. Shoji, J. Org. Chem., 2002, 67, 9443.

DOI:10.1021/jo025641m
[1] Total Synthesis of (+)-Epoxyquinols A and B
M. Shoji, J. Yamaguchi, H. Kakeya, H. Osada, Y. Hayashi, Angew. Chem. Int. Ed., 2002, 41, 3192.

DOI:10.1002/1521-3773(20020902)41:17%3C3192::AID-ANIE3192%3E3.0.CO;2-E

Selected as Hot paper in Angew. Chem. Int. Ed.

【総説、解説記事】

[9] Nickel-Catalyzed Direct Coupling of Heteroarenes

Junichiro Yamaguchi, Kei Muto, Kazuma Amaike, Takuya Yamamoto, and Kenichiro Itami

J. Synth. Org. Chem. Jpn. 201371,  576. DOI:10.5059/yukigoseikyokaishi.71.576

[8] Decarbonylative C–H Biaryl Coupling (Japanese)

Junichiro Yamaguchi and Kenichiro Itami

Kagaku 2013, 68, 35. [Link]

[7] Recent Progress in Nickel-Catalyzed Biaryl Coupling

Junichiro Yamaguchi, Kei Muto, and Kenichiro Itami

Eur. J. Org. Chem. 2013, 19–30. DOI: 10.1002/ejoc.201200914 【detail

Most Accessed Articles (January 2013).

[7] Synthesis of Bioactive Compounds through C-H Bond Functionalization

Junichiro Yamaguchi and Kenichiro Itami

Fine Chemicals 2012, 41, 38.

[5] C-H Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals

Junichiro Yamaguchi, Atsushi D. Yamaguchi, and Kenichiro Itami

Angew. Chem. Int. Ed. 201251, 8960–9009.  10.1002/anie.201201666 【detail

Selected as the Cover of the Issue.
Highlighted in Chemistry ViewsMost Accessed Articles #1 (August2012).

[4] Synthesis of Bioactive Compounds through C-H Bond Functionalization (Japanese)

Junichiro Yamaguchi, Kenichiro Itami, Catalysts & Catalysis, 2011, 53, 293.  Link 

Most-Accessed Articles

[3]  Syntheses of Fumagillin and Ovalicin

Junichiro Yamaguchi, Yujiro Hayashi, Chem. Eur. J., 201016, 3884.

DOI: 10.1002/chem.200902433

[2] Asymmetric Total Synthesis of a Natural Product Using Catalytic Enantioselective Stereoablative Reactions (Japanese)

Junichiro Yamaguchi, J.  Synth. Org. Chem., Jpn, 200967,166.

[1]スクリプス研究所Phil Baran研究室

Junichiro Yamaguchi, Organomet News, 2009, 16.

【その他科学及び化学啓蒙活動】

化学ポータルサイトChem-Station 代表

【書籍】

[4] New Cross-coupling Reactions through Nickel Catalysis

Junichiro Yamaguchi, Kazuma Amaike, Kei Muto, and Kenichiro Itami

Catalysis2013, 624.

[3] Biaryl Synthesis through Metal-Catalyzed C-H Arylation

Junichiro Yamaguchi and Kenichiro Itami

Metal Catalyzed Cross-Coupling Reactions and More; Wiley-VCH, 2013.

[2] 2006-2014 スーパー合格 過去問+本年度予想 技術士第一次試験 基礎・適性科目対策 、秀和システム(関連書籍計8冊)

[1] 2007 図解入門 よくわかる最新元素の基本と仕組み,秀和システム

【記事】

[10] 「化学の面白さと可能性」、山口潤一郎、化学経済2014年10月号 [Link]

[9] 人が集まる「科学コミュニケーション」の秘訣、インタビュー 、化学と工業、2014年7月号, 579.

[8] 「若手研究者交流の場をつくるChem-Stationイブニングミキサーのチャレンジ」山口潤一郎 2014年6月号 [Link]

[7]「 化学教育のためのインターネット活用術」 山口潤一郎、化学と教育 2014年, 5月号 230.

[6] 「特集 達人が語る◯◯の楽しみ方ー情報収集を楽しもう」山口潤一郎 「化学」(化学同人)2013年4月号

[5] 「炭素‒水素結合直接変換を鍵とする生物活性物質の合成」、山口潤一郎、化学と工業「飛翔する若手研究者」2012年12月号, 952.

[4]「続・化学研究ライフハック」、山口潤一郎、望田 憲嗣「化学」(化学同人)2011年12月号

[3]「院試で学ぶ有機化学の基礎」、山口潤一郎、生長幸之助(隔月で共著)「現代化学」(東京化学同人)2011年4月号 6月号 8月号 10月号 12月号

[2] 「化学研究ライフハック」、山口潤一郎「化学」(化学同人)特集 2010年9月号

[1]「 化学とウェブのフュージョン」、山口潤一郎「化学」(化学同人)巻頭言 2010年4月号

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