Atsushi Akao - Concepedia

Author

Atsushi Akao

Merck & Co., Inc., Rahway, NJ, USA (United States)

Also Known As

A. Akao, Atsushi Akao

Publications

485

Citations

H-Index

Concepts

All Affiliations

Merck & Co., Inc., Rahway, NJ, USA (United States)Nagoya University

About

Atsushi Akao is an author at Merck & Co., Inc., Rahway, NJ, USA (United States) specializing in pharmacology, organic chemistry, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	247
2	Natural Sciences	5	5	211
3	Biochemistry	4	4	173
4	Engineering	3	3	63
5	Biomolecular Engineering	1	1	13

Atsushi Akao

Publications

474

Citations

H-Index

Page 1

	Year	Citations
Synthesis of a Muscarinic Receptor Antagonist via a Diastereoselective Michael Reaction, Selective Deoxyfluorination and Aromatic Metal−Halogen Exchange Reaction Toshiaki Mase, Ioannis N. Houpis, Atsushi Akao, The Journal of Organic Chemistry	2001	92
Cytotoxicity and actin-depolymerizing activity of aplyronine A, a potent antitumor macrolide of marine origin, and its analogs Hideo Kigoshi, Kiyotake Suenaga, Masaki Takagi, Tetrahedron Potent Antitumor MacrolideMedicinal ChemistryPharmaceutical ChemistryBiochemistryNatural Sciences	2002	67
Cytotoxicity and actin depolymerizing activity of aplyronine A, a potent antitumor macrolide of marine origin, and the natural and artificial analogs Kiyotake Suenaga, Noriyuki Kamei, Youko Okugawa, Bioorganic & Medicinal Chemistry Letters Medicinal ChemistryBiochemistryMedicineNatural SciencesMechanism Of Action	1997	58
Efficient Synthesis of 1,4-Diaryl-5-methyl-1,2,3-triazole, A Potential mGluR1 Antagonist, and the Risk Assessment Study of Arylazides Takayuki Tsuritani, Hiroo Mizuno, Nobuaki Nonoyama, Organic Process Research & Development Medicinal ChemistryMglur1 Antagonist 1HeterocyclicN-selective CyclizationMedicine	2009	38
Highly chemoselective reduction using a Rh/C–Fe(OAc)2 system: practical synthesis of functionalized indoles Atsushi Akao, Kimihiko Sato, Nobuaki Nonoyama, Tetrahedron Letters Oxygen Reduction ReactionChemical EngineeringPractical SynthesisEngineeringFunctionalized Indoles	2005	37
Practical synthesis of a potent indolocarbazole-based, DNA topoisomerase inhibitor Atsushi Akao, Shouichi Hiraga, Takehiko Iida, Tetrahedron Medicinal ChemistryDna Topoisomerase InhibitorMedicineDrug DevelopmentPharmacology	2001	34
Practical Asymmetric Synthesis of a Selective Endothelin A Receptor (ETA) Antagonist Zhiguo J. Song, Matthew Zhao, Lisa Frey, Organic Letters Chromotography-free Asymmetric SynthesisMolecular PharmacologyMedicinal ChemistryBioorganic ChemistryBiochemistry	2001	31
A Versatile One-Pot Synthesis of 4-Aryl-1,5-disubstituted 1,2,3-Triazoles via 1,3-Dipolar Cycloaddition Followed by Negishi Reaction under New Conditions Atsushi Akao, Takayuki Tsuritani, Satoshi Kii, Synlett Versatile One-pot Synthesis4-Aryl-1,5-disubstituted 1,2,3-TriazolesDerivativesHeterocyclicSeveral Derivatives	2006	28
Asymmetric synthesis of a selective endothelin A receptor antagonist Yoshiaki Kato, Kenji Niiyama, Takayuki Nemoto, Tetrahedron Functional SelectivityMedicineAsymmetric SynthesisReceptor (Biochemistry)Pharmacological Agent	2002	19
Bromine–magnesium exchange of 5-bromo-2-picoline via an organomagnesium complex nBu2iPrMgLi: a new preparation methodology of functionalized picolines under noncryogenic conditions Satoshi Kii, Atsushi Akao, Takehiko Iida, Tetrahedron Letters Inorganic ChemistryBiochemistryNatural SciencesOrganomagnesium Complex Nbu2iprmgliBromine–magnesium Exchange	2006	17

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