607356-91-2Relevant academic research and scientific papers
Total synthesis of amino-functionalized calphostin analogs as potent and selective inhibitors of protein kinase C (PKC)
Kim, Hyoyeon,Song, Choon-Ho,Kim, Dae-Hyuk,Jung, Nam-Gin,Lee, Seung-Jae,Kim, Beom-Tae
, p. 1586 - 1592 (2016)
As potential protein kinase C (PKC) inhibitors and photodynamic agents, the novel amino-functionalized calphostin analog 1,12-bis((benzoyl-amino)methyl)-3,10-perylenequinone was successfully prepared by dimerization of the key intermediate 3-(benzoylamino
A total synthesis of yellowish aphid pigment furanaphin through fries rearrangement assisted by boron trifluoride-acetic acid complex
Nishimura, Taichi,Iwata, Takeki,Maegawa, Hironori,Nishii, Takeshi,Matsugasako, Masami,Kaku, Hiroto,Horikawa, Mitsuyo,Inai, Makoto,Tsunoda, Tetsuto
scheme or table, p. 1789 - 1792 (2012/08/29)
The yellowish aphid pigment furanaphin, isolated from Aphis spiraecola and possessing cytotoxicity against HL-60 (human promyelocytic leukemia-60) cells, was synthesized by utilizing the Fries rearrangement assisted with a BFmiddot;2AcOH complex as a key step. It was confirmed that the complex effectively mediated the reaction even though the compounds had an electron-withdrawing substituent.
