58476-04-3Relevant academic research and scientific papers
INDOLIZINE DERIVATIVES AS PHOSHOINOSITIDE 3-KINASES INHIBITORS
-
Paragraph 0575; 0576; 0581; 0582, (2015/12/31)
Compounds of formula (I), defined herein, inhibit phosphoinositide 3-kinases (PI3K) and are useful for the treatment of disorders associated with PI3K enzymes.
Discovery of a full-color-tunable fluorescent core framework through direct C-H (hetero)arylation of N-heterocycles
Liu, Bo,Wang, Zhi,Wu, Ningjie,Li, Mingliang,You, Jingsong,Lan, Jingbo
, p. 1599 - 1603 (2012/03/10)
All the colors of the rainbow! A full coverage of emission wavelengths in the visible region (405-616 nm) with large Stokes shifts in C3-Indo-Fluor may be straightforwardly and succinctly achieved by the palladium-catalyzed direct C-H arylation of indolizines at the C3 position of the pyrrole ring (see figure). The fluorophores have successfully marked A375 cells. Copyright
HETEROCYCLIC SYNTHESIS BY ELECTROCYCLIZATION OF EXTENDED DIPOLES: A NOVEL ACCESS TO THE INDOLIZINE AND QUINOLIZINE SYSTEMS
Eberbach, Wolfgang,Maier, Wolfram
, p. 5591 - 5594 (2007/10/02)
On thermal activation α-butenynyl substituted pyridine-N-oxides 4 undergo a multistep rearrangement affording 4-oxo-4H-quinolizines (8) and 2-acylindolizines (9).In the geometrical isomeriziation of E-4 to Z-4 annulated isoxazolidines (7) are involved as unstable intermediates.
