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Tomohiro Tsujita
Institution:
Merck & Co., Inc., Rahway, NJ, USA (United States)
Observed institutions:
Merck & Co., Inc., Rahway, NJ, USA (United States),
Keio University
OpenAlex ID:
A5078860532
Asymmetric Total Syntheses of (+)-Cheimonophyllon E and (+)-Cheimonophyllal
2002
·
Ken-ichi Takao
, Tomohiro Tsujita
, et al.
·
The Journal of Organic Chemistry
·
30
A Novel Class of Cycloalkano[b]pyridines as Potent and Orally Active Opioid Receptor-like 1 Antagonists with Minimal Binding Affinity to the hERG K+Channel
2008
·
Takashi Yoshizumi
, Hirobumi Takahashi
, et al.
·
Journal of Medicinal Chemistry
·
26
Synthetic studies of pestalotiopsin A: asymmetric synthesis of the 2-oxabicyclo[3.2.0]heptane substructure
2005
·
Ken-ichi Takao
, Hiroshi Saegusa
, et al.
·
Tetrahedron Letters
·
26
Design, synthesis, and structure–activity relationship study of a novel class of ORL1 receptor antagonists based on N-biarylmethyl spiropiperidine
2008
·
Takashi Yoshizumi
, Hiroshi Miyazoe
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
17
Discovery of novel arylpyrazole series as potent and selective opioid receptor-like 1 (ORL1) antagonists
2009
·
Kensuke Kobayashi
, Minaho Uchiyama
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
11
Total synthesis of (+)-cheimonophyllon E, a bisabolane sesquiterpenoid
2001
·
Ken-ichi Takao
, Manabu Hara
, et al.
·
Tetrahedron Letters
·
7
Identification of MK-1925: A selective, orally active and brain-penetrable opioid receptor-like 1 (ORL1) antagonist
2009
·
Kensuke Kobayashi
, Tomohiro Tsujita
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
4
Practical Syntheses of Enantiomerically Pure Key Intermediates of Opioid Receptor-like 1 (ORL1) Antagonists
2009
·
Takashi Yoshizumi
, Hideo Kigoshi
, et al.
·
Synthesis
·
4
Asymmetric Total Syntheses of (+)‐Cheimonophyllon E (I) and (+)‐Cheimonophyllal (II).
2003
·
Ken‐ichi Takao
, Tomohiro Tsujita
, et al.
·
ChemInform
ChemInform Abstract: Total Synthesis of (+)‐Cheimonophyllon E, a Bisabolane Sesquiterpenoid.
2001
·
Ken‐ichi Takao
, Manabu Hara
, et al.
·
ChemInform
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Works count:
10
Citation count:
125
H-index:
6
I10-index:
5
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