Palladium-Catalyzed Arylation and Heteroarylation of Indolizines
作者:Choul-Hong Park、Victoria Ryabova、Ilya V. Seregin、Anna W. Sromek、Vladimir Gevorgyan
DOI:10.1021/ol049866q
日期:2004.4.1
A highly effective protocol for palladium-catalyzed selective arylation and heteroarylation of indolizines at C-3 has been developed. Mechanistic studies unambiguously support an electrophilic substitution pathway for this transformation.
INDOLIZINE DERIVATIVES AS PHOSPHOINOSITIDE 3-KINASES INHIBITORS
申请人:Chiesi Farmaceutici S.p.A.
公开号:EP3157920B1
公开(公告)日:2019-08-07
US9527869B2
申请人:——
公开号:US9527869B2
公开(公告)日:2016-12-27
[EN] INDOLIZINE DERIVATIVES AS PHOSHOINOSITIDE 3-KINASES INHIBITORS<br/>[FR] DÉRIVÉS D'INDOLIZINE SERVANT D'INHIBITEURS DES PHOSHOINOSITIDE 3-KINASES
申请人:CHIESI FARMA SPA
公开号:WO2015193263A1
公开(公告)日:2015-12-23
The invention relates to compounds inhibiting phosphoinositide 3-kinases (PI3K), to pharmaceutical compositions comprising them and therapeutic use thereof in the treatment of disorders associated with PI3K enzymes.
INDOLIZINE DERIVATIVES AS PHOSHOINOSITIDE 3-KINASES INHIBITORS
申请人:CHIESI FARMACEUTICI S.P.A.
公开号:US20150361100A1
公开(公告)日:2015-12-17
Compounds of formula (I), defined herein, inhibit phosphoinositide 3-kinases (PI3K) and are useful for the treatment of disorders associated with PI3K enzymes.