Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Takanori Yasukouchi"'
Autor:
Masunobu Sugimura, Masaki Saito, Takanori Yasukouchi, Shinichi Kawajiri, Masayuki Ito, Kei-ichi Kawagoe, Tetuya Mimura, Fusako Kito, Toshiaki Tatematu, Yoshiyuki Yoneda
Publikováno v:
ChemInform. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e4e59aada0de31af02b171a3daaee6c
https://doi.org/10.1002/chin.200220046
https://doi.org/10.1002/chin.200220046
Autor:
Masaki Saito, Yoshiyuki Yoneda, Shinichi Kawajiri, Kei-ichi Kawagoe, Toshiaki Tatematu, Masayuki Ito, Takanori Yasukouchi, Tetuya Mimura, Masunobu Sugimura, Fusako Kito
Publikováno v:
Bioorganicmedicinal chemistry. 10(5)
We designed and synthesized a series of the polyamine derivatives as potent Ca2+-permeable AMPA receptor antagonists. In the course of this study, we found that the polyamine derivatives exhibited strong hypotensive activity which was undesirable act
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::695b3576d7e3df3d7cc9b724d2c7279f
https://pubmed.ncbi.nlm.nih.gov/11886798
https://pubmed.ncbi.nlm.nih.gov/11886798
Autor:
Ken Kanematsu, Takanori Yasukouchi
Publikováno v:
ChemInform. 21
The first total synthesis of (±)- cis -trikentrin B (1) based on a new indole synthesis via the intramolecular Diels-Alder reaction of 1,2,3-trisubstituted allenic dienamide (8) is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d043992fba065172de1d13fc6466686f
https://doi.org/10.1002/chin.199031300
https://doi.org/10.1002/chin.199031300
Autor:
Ken Kanematsu, Takanori Yasukouchi
Publikováno v:
ChemInform. 21
An efficient approach to a novel tricyclic indole, the basic skeleton of cis-trikentrins (10), utilizing an allene intramolecular Diels–Alder reaction of a 2,3-disubstituted allenic dienamide (4), is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::052e7e37990e153c07c08a64de1f02ff
https://doi.org/10.1002/chin.199002174
https://doi.org/10.1002/chin.199002174
Autor:
Takanori Yasukouchi, Ken Kanematsu
Publikováno v:
Tetrahedron Letters. 30:6559-6562
The first total synthesis of (±)- cis -trikentrin B (1) based on a new indole synthesis via the intramolecular Diels-Alder reaction of 1,2,3-trisubstituted allenic dienamide (8) is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2146fc52e251961f2f673031a8b9af93
https://doi.org/10.1016/s0040-4039(01)89021-3
https://doi.org/10.1016/s0040-4039(01)89021-3
Publikováno v:
Tetrahedron Letters. 27:1837-1840
A new development of efficient indole synthesis via allene intramolecular cycloaddition strategy is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bd3c3023773bf7a2ebbebf255399ad1
https://doi.org/10.1016/s0040-4039(00)84389-0
https://doi.org/10.1016/s0040-4039(00)84389-0
Publikováno v:
Tetrahedron Letters. 28:5895-5898
Combination of the indole synthesis (CD ring) via intramolecular Diels-Alder reaction of 3-substituted allenic dienamide ( 5 ) and base-catalyzed intramolecular N-acylation (B ring formation) provides a simple route to pyrrolophenanthridone alkalo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79d6478df36114c52f8f6343a8ad7c92
https://doi.org/10.1016/s0040-4039(01)81084-4
https://doi.org/10.1016/s0040-4039(01)81084-4
Publikováno v:
ChemInform. 19
Combination of the indole synthesis (CD ring) via intramolecular Diels-Alder reaction of 3-substituted allenic dienamide ( 5 ) and base-catalyzed intramolecular N-acylation (B ring formation) provides a simple route to pyrrolophenanthridone alkalo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a44ef217b73d0c686450f225b9a819ae
https://doi.org/10.1002/chin.198818315
https://doi.org/10.1002/chin.198818315
Autor:
Takanori Yasukouchi, Ken Kanematsu
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :1404
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a31a5fad2a1572609273e4fa9bcf56f5
https://doi.org/10.1039/c39890001404
https://doi.org/10.1039/c39890001404
Autor:
Takanori Yasukouchi, Ken Kanematsu
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :953
An efficient approach to a novel tricyclic indole, the basic skeleton of cis-trikentrins (10), utilizing an allene intramolecular Diels–Alder reaction of a 2,3-disubstituted allenic dienamide (4), is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a23290b13367d8cf5205926bc534f9cc
https://doi.org/10.1039/c39890000953
https://doi.org/10.1039/c39890000953