153274-63-6Relevant articles and documents
Indolizine studies. Part 4. Kinetics and mechanism for the formation of indolizines via thermal cyclisation of 2-pyridyl derivatives
Deane, Philip O.,George, Rosemary,Kaye, Perry T.
, p. 3871 - 3876 (1998)
The influence of substituents and temperature on the thermal cyclisation of 3-acetoxy-2-methylene-3-(2-pyridyl)propanoic esters and analogues has been explored using 1H NMR spectroscopy, and mechanistic proposals for the formation of the resulting indolizines are presented.
Catalytic Asymmetric Conjugate Addition of Indolizines to α,β-Unsaturated Ketones
Correia, José Tiago Menezes,List, Benjamin,Coelho, Fernando
supporting information, p. 7967 - 7970 (2017/06/27)
A catalytic enantioselective conjugate addition of indolizines to enones is described. The chiral phosphoric acid (S)-TRIP activates α,β-unsaturated ketones, thereby promoting an enantioface-differentiating attack by indolizines. Using this reaction, several alkylated indolizines were synthesized in good yields and with enantiomeric ratios of up to 98:2.
INDOLIZINE DERIVATIVES AS PHOSHOINOSITIDE 3-KINASES INHIBITORS
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Paragraph 0289; 0290, (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.
