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Metal–organic frameworks as solid catalysts for the synthesis of nitrogen-containing heterocycles
Metal–organic frameworks (MOFs) are finding increasing application as solid catalysts for
liquid phase reactions leading to the synthesis of fine chemicals. In the present review we …
liquid phase reactions leading to the synthesis of fine chemicals. In the present review we …
Naphtho [2, 1-b] furan derived triazole-pyrimidines as highly potential InhA and Cytochrome c peroxidase inhibitors: synthesis, DFT calculations, drug-likeness profile …
DL Roopa, K Shyamsunder, P Karunakar… - Journal of Molecular …, 2023 - Elsevier
Napthofuran and its fused heterocyclic derivatives evaluated with varied biological activity
functional groups comprise an important class of compounds for new chemical entities. We …
functional groups comprise an important class of compounds for new chemical entities. We …
Review on synthetic approaches towards barbituric acids‐based furo[2,3‐d]pyrimidines
A Olyaei, M Sadeghpour - Journal of Heterocyclic Chemistry, 2023 - Wiley Online Library
Pyrimidine annulated five‐membered heterocyclic scaffolds containing oxygen as
furopyrimidine, particularly furo [2, 3‐d] pyrimidine derivatives are an important class of …
furopyrimidine, particularly furo [2, 3‐d] pyrimidine derivatives are an important class of …
[PDF][PDF] Synthesis and antimicrobial evaluation of some new thienopyrimidine derivatives
MH Bhuiyan, KM Rahman, K Hossain… - ACTA …, 2006 - core.ac.uk
Reaction of heteroaromatic o-aminonitrile with ethyl N--[bis (methylthio) methylene] amino
acetate resulted in annelation of a thieno [3, 2-e] imidazo [1, 2-c] pyrimidine moiety in a one …
acetate resulted in annelation of a thieno [3, 2-e] imidazo [1, 2-c] pyrimidine moiety in a one …
[PDF][PDF] Antibacterial, antifungal and antiviral activities of pyrimido [4, 5-d] pyrimidine derivatives through computational approaches
Pyrimido [4, 5-d] pyrimidine conveys antimicrobial activity against various micro pathogens
having functionalized properties. As a result, this study has designed to illustrate the …
having functionalized properties. As a result, this study has designed to illustrate the …
Synthetic utility of bifunctional thiophene derivatives and antimicrobial evaluation of the newly synthesized agents
AA Abu-Hashem, KM Abu-Zied… - Monatshefte für Chemie …, 2011 - Springer
The key intermediate ethyl 2-amino-5-benzoyl-4-methylthiophene-3-carboxylate was
prepared by a Gewald reaction starting from benzoylacetone, sulfur, and ethyl cyanoacetate …
prepared by a Gewald reaction starting from benzoylacetone, sulfur, and ethyl cyanoacetate …
Metal-organic framework Cu3 (BTC) 2 (H2O) 3 catalyzed Aldol synthesis of pyrimidine-chalcone hybrids
NB Pathan, AM Rahatgaonkar… - Catalysis Communications, 2011 - Elsevier
A typical metal organic framework,[Cu 3 (BTC) 2 (H 2 O) 3, BTC= 1, 3, 5-benzene
tricarboxylate] has been used for the synthesis of pyrimidine-chalcones. We have explored a …
tricarboxylate] has been used for the synthesis of pyrimidine-chalcones. We have explored a …
One-pot three component isocyanide-based reaction: Synthesis of novel tetracyclic fused furo [2′, 3′: 4, 5] pyrimido [2, 1-b][1, 3] benzothiazole
M Zangouei, AA Esmaeili, JT Mague - Tetrahedron, 2017 - Elsevier
A rapid, efficient and benign protocol has been developed for the construction of potentially
biologically active furo [2′, 3′: 4, 5] pyrimido [2, 1-b][1, 3] benzothiazole derivatives as …
biologically active furo [2′, 3′: 4, 5] pyrimido [2, 1-b][1, 3] benzothiazole derivatives as …
[HTML][HTML] Furo [2, 3-d] pyrimidine based derivatives as kinase inhibitors and anticancer agents
Furopyrimidines are fused heterocyclic ring systems. Structurally, they are bioisoteres to
purines and exerting pharmacological actions in various aspects. They are known to play an …
purines and exerting pharmacological actions in various aspects. They are known to play an …
Furan- and Furopyrimidine-Based Derivatives: Synthesis, VEGFR-2 Inhibition, and In Vitro Cytotoxicity
AH Abd El-Haleem, MAE Kassem… - ACS Medicinal …, 2024 - ACS Publications
New derivatives 4a–d, 6, 7a–d, 8a–c, 9, 11a, 11b, 12a–f, 13a–c, and 14 were synthesized
and evaluated for their VEGFR-2 inhibition. Compounds 4c, 7b, and 7c showed remarkable …
and evaluated for their VEGFR-2 inhibition. Compounds 4c, 7b, and 7c showed remarkable …