TY - JOUR
T1 - 4H-Pyrido[1,2-a]pyrimidin-4-one, biologically important fused heterocyclic scaffold
T2 - Synthesis and functionalization
AU - Bhawale, Rajesh T.
AU - Chillal, Abhinay S.
AU - Kshirsagar, Umesh A.
N1 - Publisher Copyright:
© 2023 Wiley Periodicals LLC.
PY - 2023/8/1
Y1 - 2023/8/1
N2 - 4H-pyrido[1,2-a]pyrimidin-4-one and their derivatives are highly bioactive and multipurpose heterocyclic motifs, having application in drugs, natural products, agrochemical, material science, and organic synthesis. The C-H functionalization of basic core structure of heterocycles have become indispensable tools that have continually increased the importance in the pharmaceutical industry for the synthesis of various useful heterocyclic molecules and their derivatives. In this review, we have provided a summary of various routes to synthesize 4H-pyrido[1,2-a]pyrimidin-4-one derivatives along with various derivatization methods such as via cross-coupling, C-H functionalization through arylation, alkenylation, sulfenylation, selenylation, phosphonation etc. taking into account the synthetic potentiality and significant influence of this scaffold in drug discovery.
AB - 4H-pyrido[1,2-a]pyrimidin-4-one and their derivatives are highly bioactive and multipurpose heterocyclic motifs, having application in drugs, natural products, agrochemical, material science, and organic synthesis. The C-H functionalization of basic core structure of heterocycles have become indispensable tools that have continually increased the importance in the pharmaceutical industry for the synthesis of various useful heterocyclic molecules and their derivatives. In this review, we have provided a summary of various routes to synthesize 4H-pyrido[1,2-a]pyrimidin-4-one derivatives along with various derivatization methods such as via cross-coupling, C-H functionalization through arylation, alkenylation, sulfenylation, selenylation, phosphonation etc. taking into account the synthetic potentiality and significant influence of this scaffold in drug discovery.
UR - http://www.scopus.com/inward/record.url?scp=85149480506&partnerID=8YFLogxK
U2 - 10.1002/jhet.4637
DO - 10.1002/jhet.4637
M3 - Review article
AN - SCOPUS:85149480506
SN - 0022-152X
VL - 60
SP - 1356
EP - 1373
JO - Journal of Heterocyclic Chemistry
JF - Journal of Heterocyclic Chemistry
IS - 8
ER -