33. Synthesis of Dragmacidin D via Direct C–H Couplings
2016-09-19_16-56-31 ishot-7-1

Mandal, D.; Yamaguchi, A. D.; Yamaguchi, J.*; Itami, K.*
J. Am. Chem. Soc.2011133, 19660–19663.
Highlights  Chemistry World. Most Read Articles (November 2011),

32. Exploitation of an Additional Hydrophobic Pocket of σ1 Receptors: Late-stage Diverse Modifications of Spirocyclic Thiophenes by C–H Functionalization
2016-09-19_16-55-18 obcmeyer

Meyer, C.; Neue, B.; Schepmann, D.; Yanagisawa, S.; Yamaguchi, J.; Würthwein, E.; Itami, K.*; Wünsch, B.*
Org. Biomol. Chem. 20119, 8016­–8029.

31. Enantioselective Total Syntheses of (–)-Palau’amine, (–)-Axinellamines, and (–)-Massadines
2016-09-19_16-54-14 ja-2011-047232_0021

Seiple, I. B.; Su, S.; Young, I. S.; Nakamura, A.; Yamaguchi, J.; Jørgensen, L; Rodriguez, R. A.; O’Malley, D. P.; Gaich, T.; Kock M.; Baran, P. S.*
J. Am. Chem. Soc. 2011, 133, 14710–14726.
Highlights Most Read Articles (October 2011)

30. Nickel-Catalyzed C–H Arylation of Azoles with Haloarenes: Scope, Mechanism, and Applications to the Synthesis of Bioactive Molecules
2016-09-19_16-52-59 ni_takuya_muto

Yamamoto, T.; Muto, K.; Komiyama, M.; Canivet, J.; Yamaguchi, J.; Itami, K.*
Chem. Eur. J. 2011, 17, 10113–10122.
DOI: 10.1002/chem.201101091
Highlights Highlighted in SYNFACTS

29. Synthesis of Bioactive Compounds through C–H Bond Functionalization
2016-09-19_16-52-12 synthCH

Yamaguchi, J.*; Itami, K.*
Catalysts and Catalysis 2011, 53, 293–298 .

28. Oxidative C–H/C–H Coupling of Azine and Indole/Pyrrole Nuclei: Palladium Catalysis and Synthesis of Eudistomin U
2016-09-19_16-50-07 atsushi_ychemlett

Yamaguchi, A. D.; Mandal, D.; Yamaguchi, J.*; Itami, K.*
Chem. Lett. 2011, 40, 555–557.
Selected as “Editor’s Choice”. Most-Accessed Articles. Highlighted in Angew. Chem. Int. Ed.

27. Oxidative Biaryl Coupling of Thiophenes and Thiazoles with Arylboronic Acids through Palladium Catalysis: Otherwise Difficult C4-Selective C–H Arylation Enabled by Boronic Acids
2016-09-19_16-48-25 mcontent-5

Kirchberg, S.; Tani, S.; Ueda, K.; Yamaguchi, J.; Studer, A.*; Itami, K.*
Angew. Chem., Int. Ed. 2011, 50, 2387–2391.

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