Concepedia

Author

Masashi Imanishi

Astellas Pharma (Japan)

Also Known As

M. IMANISHI, Masashi Imanishi

14

Publications

279

Citations

9

H-Index

15

Concepts

All Affiliations

Astellas Pharma (Japan)Monell Chemical Senses CenterUniversity of Pennsylvania
MI

About

Masashi Imanishi is an author at Astellas Pharma (Japan) specializing in biochemistry, alpha-adrenergic pharmacology, and drug discovery.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Biochemistry

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27

2

Engineering

1

1

16

3

Medicine

1

1

11

4

Natural Sciences

1

1

16

5

Biomolecular Engineering

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1

16

Masashi Imanishi

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9

Publications

272

Citations

9

H-Index

YearCitations

Total Synthesis of (−)-Mandelalide A Exploiting Anion Relay Chemistry (ARC): Identification of a Type II ARC/CuCN Cross-Coupling Protocol

Minh H. Nguyen, Masashi Imanishi, Taichi Kurogi,

Journal of the American Chemical Society

2016

73

Lipase-Catalyzed Domino Kinetic Resolution/Intramolecular Diels–Alder Reaction: One-Pot Synthesis of Optically Active 7-Oxabicyclo[2.2.1]heptenes from Furfuryl Alcohols and -Substituted Acrylic Acids

Shuji Akai, Tadaatsu Naka, Sohei Omura,

Chemistry - A European Journal

2002

46

Discovery of a Novel Series of Biphenyl Benzoic Acid Derivatives as Potent and Selective Human β<sub>3</sub>-Adrenergic Receptor Agonists with Good Oral Bioavailability. Part I

Masashi Imanishi, Yasuyo Tomishima, Shinji Itou,

Journal of Medicinal Chemistry

2008

41

Discovery of a Novel Series of Biphenyl Benzoic Acid Derivatives as Highly Potent and Selective Human β3 Adrenergic Receptor Agonists with Good Oral Bioavailability. Part II

Masashi Imanishi, Shinji Itou, Kenichi Washizuka,

Journal of Medicinal Chemistry

2008

30

Synthetic Access to the Mandelalide Family of Macrolides: Development of an Anion Relay Chemistry Strategy

Minh H. Nguyen, Masashi Imanishi, Taichi Kurogi,

The Journal of Organic Chemistry

2018

24

Discovery of a Novel Series of Benzoic Acid Derivatives as Potent and Selective Human β<sub>3</sub>Adrenergic Receptor Agonists with Good Oral Bioavailability. 3. Phenylethanolaminotetraline (PEAT) Skeleton Containing Biphenyl or Biphenyl Ether Moiety

Masashi Imanishi, Yutaka Nakajima, Yasuyo Tomishima,

Journal of Medicinal Chemistry

2008

21

Asymmetric Diels–Alder reaction via enzymatic kinetic resolution using ethoxyvinyl methyl fumarate

Yasuyuki Kita, Masashi Imanishi, Shuji Akai,

Chemical Communications

1998

16

Discovery of highly potent and selective biphenylacylsulfonamide-based β3-adrenergic receptor agonists and molecular modeling based on the solved X-ray structure of the β2-adrenergic receptor: Part 6

Kouji Hattori, Masaya Orita, Susumu Toda,

Bioorganic & Medicinal Chemistry Letters

2009

11

Discovery of Highly Potent and Selective Biphenylacylsulfonamide-Based β<sub>3</sub>-Adrenergic Receptor Agonists and Evaluation of Physical Properties as Potential Overactive Bladder Therapies: Part 5

Kouji Hattori, Susumu Toda, Masashi Imanishi,

Journal of Medicinal Chemistry

2009

10

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