Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Tamiko Ito"'
Autor:
Reo Maeda, Mitsutoshi Nakamura, Haruka Yamamoto, Shunsuke Shimaoka, Hironao Iida, Ryo Hatori, Kenji Matsuno, Ayumi Ozaki, Naotaka Nakazawa, Takashi Okumura, Masashi Yoshida, Takaaki Maeda, Akira Ishio, Kiichiro Taniguchi, Tamiko Ito, Junpei Kuroda
Publikováno v:
Mechanisms of development. 128(11-12)
Many animals develop left–right (LR) asymmetry in their internal organs. The mechanisms of LR asymmetric development are evolutionarily divergent, and are poorly understood in invertebrates. Therefore, we studied the genetic pathway of LR asymmetri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ae7d6e4ebbbda2bdcb33aac421f1cb2
https://pubmed.ncbi.nlm.nih.gov/22198363
https://pubmed.ncbi.nlm.nih.gov/22198363
Publikováno v:
ChemInform. 22
Treatment of N-[o-(alk-1-enyl)phenyl]-2-(methylsulfinyl)acetamides with trifluoroacetic anhydride gave 2(1H)-quinolinones or 2H-1-benzazepin-2-ones, depending upon the position of the substituents on the alkene double bond.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24259e5ad1cda377cb74450754ec9af6
https://doi.org/10.1002/chin.199142208
https://doi.org/10.1002/chin.199142208
Publikováno v:
Chemical and Pharmaceutical Bulletin. 38:3331-3334
Treatment of N-[o-(alk-1-enyl)phenyl]-2-(methylsulfinyl)acetamides with trifluoroacetic anhydride gave 2(1H)-quinolinones or 2H-1-benzazepin-2-ones, depending upon the position of the substituents on the alkene double bond.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62acf3c2881d9bb3da6c58f316e5f79c
https://doi.org/10.1248/cpb.38.3331
https://doi.org/10.1248/cpb.38.3331