[HTML][HTML] Transition metal-catalysed carbene-and nitrene transfer to carbon monoxide and isocyanides
Transition metal-catalysed carbene-and nitrene transfer to the C1-building blocks carbon
monoxide and isocyanides provides heteroallenes (ie ketenes, isocyanates, ketenimines …
monoxide and isocyanides provides heteroallenes (ie ketenes, isocyanates, ketenimines …
An appraisal of anticancer activity with structure–activity relationship of quinazoline and quinazolinone analogues through EGFR and VEGFR inhibition: A review
Cancer is one of the leading causes of death. Globally a huge number of deaths and new
incidences are reported annually. Heterocyclic compounds have been proved to be very …
incidences are reported annually. Heterocyclic compounds have been proved to be very …
[HTML][HTML] Recent advances in palladium-catalyzed isocyanide insertions
Isocyanides have long been known as versatile chemical reagents in organic synthesis.
Their ambivalent nature also allows them to function as a CO-substitute in palladium …
Their ambivalent nature also allows them to function as a CO-substitute in palladium …
Silver-catalyzed cascade cyclization reaction of isocyanides with sulfoxonium ylides: synthesis of 3-aminofurans and 4-aminoquinolines
YX Liang, M Yang, BW He, YL Zhao - Organic Letters, 2020 - ACS Publications
A silver-catalyzed cascade cyclization reaction of isocyanides with sulfoxonium ylides has
been developed for the first time. This reaction provides a new and efficient method for the …
been developed for the first time. This reaction provides a new and efficient method for the …
Design, synthesis, biological evaluation of 3, 5-diaryl-4, 5-dihydro-1H-pyrazole carbaldehydes as non-purine xanthine oxidase inhibitors: Tracing the anticancer …
Xanthine oxidase (XO) has been primarily targeted for the development of anti-
hyperuriciemic/anti-gout agents as it catalyzes the conversion of xanthine and hypoxanthine …
hyperuriciemic/anti-gout agents as it catalyzes the conversion of xanthine and hypoxanthine …
Quinazolines annelated at the N (3)-C (4) bond: synthesis and biological activity
EV Nosova, GN Lipunova, YV Permyakova… - European Journal of …, 2024 - Elsevier
This review covers article and patent data obtained mostly within the period 2013− 2023 on
the synthesis and biological activity of quinazolines [c]-annelated by five-and six-membered …
the synthesis and biological activity of quinazolines [c]-annelated by five-and six-membered …
Transition‐Metal‐Catalyzed Cross‐Coupling and Sequential Reactions of Azides with Isocyanides
Z Zhang, P Tan, W Chang… - Advanced Synthesis & …, 2021 - Wiley Online Library
Transition‐metal‐catalyzed cross‐coupling reaction of azides with isocyanides, as a new
type of nitrene transformation, has become an expeditious method to prepare carbodiimides …
type of nitrene transformation, has become an expeditious method to prepare carbodiimides …
[HTML][HTML] Design and Synthesis of Non-Covalent Imidazo[1,2-a]quinoxaline-Based Inhibitors of EGFR and Their Anti-Cancer Assessment
A series of 30 non-covalent imidazo [1, 2-a] quinoxaline-based inhibitors of epidermal
growth factor receptor (EGFR) were designed and synthesized. EGFR inhibitory assessment …
growth factor receptor (EGFR) were designed and synthesized. EGFR inhibitory assessment …
E-pharmacophore guided discovery of pyrazolo [1, 5-c] quinazolines as dual inhibitors of topoisomerase-I and histone deacetylase
In the quest to ameliorate the camptothecin (CPT) downsides, we expedite to search for
stable non-CPT analogues among 11 motifs of pyrazoloquinazolines reported. E …
stable non-CPT analogues among 11 motifs of pyrazoloquinazolines reported. E …
Anticancer potential of some imidazole and fused imidazole derivatives: Exploring the mechanism via epidermal growth factor receptor (EGFR) inhibition
Imidazole-based epidermal growth factor receptor (EGFR) inhibitors were computationally
designed and synthesized. All the compounds were assessed for their anti-proliferative …
designed and synthesized. All the compounds were assessed for their anti-proliferative …