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PubPharm (13)
1
Ten-Gram-Scale Total Synthesis of the Anticancer Drug Candidate E7130 to Supply Clinical Trials
enthalten in:
Organic letters
| 2024
von
Kaburagi, Y.
|
Kira, K.
|
Yahata, K.
| +28
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2
Identification of a novel ALDH1A3-selective inhibitor by a chemical probe with unrelated bioactivity : An approach to affinity-based drug target discovery
enthalten in:
Chemical biology & drug design
| 2023
von
Kamiyama, H.
|
Miyano, M.
|
Ito, D.
| +6
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3
Identification of a novel ALDH1A3‐selective inhibitor by a chemical probe with unrelated bioactivity : An approach to affinity‐based drug target discovery
enthalten in:
Chemical Biology & Drug Design
| 2023
von
Kamiyama, H.
|
Miyano, M.
|
Ito, D.
| +6
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4
A landmark in drug discovery based on complex natural product synthesis
enthalten in:
Scientific reports
| 2019
von
Kawano, S.
|
Ito, K.
|
Yahata, K.
| +18
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5
New syntheses of E7389 C14-C35 and halichondrin C14-C38 building blocks : reductive cyclization and oxy-Michael cyclization approaches
enthalten in:
Journal of the American Chemical Society
| 2009
von
Dong, C.
|
Henderson, J.
|
Kaburagi, Y.
| +6
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6
Effective Procedure for Selective Ammonolysis of Monosubstituted Oxiranes : Application to E7389 Synthesis
enthalten in:
Tetrahedron letters
| 2007
von
Kaburagi, Y.
|
Kishi, Y.
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7
Operationally simple and efficient workup procedure for TBAF-mediated desilylation : application to halichondrin synthesis
enthalten in:
Organic letters
| 2007
von
Kaburagi, Y.
|
Kishi, Y.
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8
Effective procedure for selective ammonolysis of monosubstituted oxiranes: application to E7389 synthesis
enthalten in:
Tetrahedron letters
| 2007
von
Kaburagi, Y.
|
Kishi, Y.
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9
Total synthesis of (-)-strychnine
enthalten in:
Journal of the American Chemical Society
| 2004
von
Kaburagi, Y.
|
Tokuyama, H.
|
Fukuyama, T.
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10
4-(tert-Butyldimethylsilyloxy)benzylidene acetal: a novel benzylidene-type protecting group for 1,2-diols
enthalten in:
Tetrahedron letters
| 2004
von
Kaburagi, Y.
|
Osajima, H.
|
Shimada, K.
| +2
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1
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halichondrin B
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