Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kazuhisa Fukuishi"'
Autor:
Airi Fujimoto, Gouji Toyokawa, Yoshimichi Koutake, Shigeru Kimura, Yosei Kawamata, Kazuhisa Fukuishi, Koji Yamazaki, Sadanori Takeo
Publikováno v:
Thoracic Cancer, Vol 12, Iss 15, Pp 2198-2204 (2021)
Abstract Background Immune checkpoint inhibitors (ICIs) have revolutionized the treatment of advanced or recurrent non‐small cell lung cancer (NSCLC). They cause immune‐related adverse events (irAEs), but the underlying mechanisms and predictors
Externí odkaz:
https://doaj.org/article/4f32ce535f44446bb8f92289d5998f61
Autor:
Yosei Kawamata, Koji Yamazaki, Gouji Toyokawa, Sadanori Takeo, Kazuhisa Fukuishi, Yoshimichi Koutake, Shigeru Kimura, Airi Fujimoto
Publikováno v:
Thoracic Cancer, Vol 12, Iss 15, Pp 2198-2204 (2021)
Thoracic Cancer
Thoracic Cancer
Background Immune checkpoint inhibitors (ICIs) have revolutionized the treatment of advanced or recurrent non‐small cell lung cancer (NSCLC). They cause immune‐related adverse events (irAEs), but the underlying mechanisms and predictors remain to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77284f4511c8ef448c92dcc95a1ecc79
https://doi.org/10.1111/1759-7714.14063
https://doi.org/10.1111/1759-7714.14063
Publikováno v:
Tetrahedron. 60:3273-3282
A new synthetic method of (−)-vallesamidine, including a unique 2,2,3-trialkylindoline skeleton, was developed by reductive radical cyclization reaction from the 2,3-dialkylindole derivative, which has been known to be an intermediate for the synth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2eedf7aedc66c779aaf68b2b1232b050
https://doi.org/10.1016/j.tet.2004.02.015
https://doi.org/10.1016/j.tet.2004.02.015
Publikováno v:
Tetrahedron Letters. 43:2385-2388
A new synthetic method of (−)-vallesamidine, including a unique 2,2,3-trialkylindoline skeleton, is developed by reductive radical cyclization reaction from the 2,3-dialkylindole derivative, which has been known to be an intermediate for the synthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff6faa7724b1c741c6d1eff996446c13
https://doi.org/10.1016/s0040-4039(02)00256-3
https://doi.org/10.1016/s0040-4039(02)00256-3
Publikováno v:
ChemInform. 33
A new synthetic method of (−)-vallesamidine, including a unique 2,2,3-trialkylindoline skeleton, is developed by reductive radical cyclization reaction from the 2,3-dialkylindole derivative, which has been known to be an intermediate for the synthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d60723c9e9f1d3d7bf51db0525a0ae94
https://doi.org/10.1002/chin.200229212
https://doi.org/10.1002/chin.200229212