29261-44-7Relevant articles and documents
DMAP-promoted in situ activation of bromoacetic acid as a 2-carbon synthon for facile synthesis of pyridines and fused pyridin-2-ones
Wang, Lu,Zhu, Gaoyuan,Tang, Weifang,Lu, Tao,Du, Ding
, p. 6510 - 6517 (2016)
A general and simple synthesis of 2,4,6-trisubstituted pyridines and fused pyridine-2-ones from bromoacetic acid is developed via a DMAP-promoted in situ activation strategy. In this protocol, readily accessible bromoacetic acid has been effectively emplo
Heterocyclic compound and organic electroluminescence device including the same
-
Paragraph 0199; 0200; 0201; 0202, (2019/02/21)
Provided is a heterocyclic compound represented by Formula 1 below, and an organic electroluminescence device including the same in an emission layer. In Formula 1, X is a direct linkage or CR2R3 , Z1to Z8 are each independently CR4 or N, at least two of
Consecutive Alkynylation-Michael Addition-Cyclocondensation (AMAC) Multicomponent Syntheses of α-Pyrones and α-Pyridones
Breuer, Natascha,Müller, Thomas J. J.
, p. 2741 - 2752 (2018/06/08)
A novel consecutive three-component synthesis of α-pyrones is based upon an alkynylation-Michael addition-cyclocondensation (AMAC) sequence, starting from (hetero)aroyl chloride and terminal alkyne to furnish the alkynone which reacts with malonates to gi
