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- Coumarin–furo[2,3-d]pyrimidone hybrid molecules targeting human liver cancer cells: synthesis, anticancer effect, EGFR inhibition and molecular docking studies. Tianshuai Wang, Yumeng Gao, Fengxu Wu, Lun Luo, Junkai Ma, Yanggen Hu
, RSC Med. Chem.
, 2024
- Elaborating piperazinyl-furopyrimidine based scaffolds as phosphoinositol-3-kinase enzyme alpha (PI3Kα) inhibitors to combat pancreatic cancer. Mai A. Mansour, Deena S. Lasheen, Hatem M. Gaber, Khaled A. M. Abouzid
, RSC Adv.
, 2020
, 10
, 32103
- Diversity oriented syntheses of fused pyrimidines designed as potential antifolates. Colin L. Gibson, Judith K. Huggan, Alan Kennedy, Lionel Kiefer, Jeong Hwan Lee, Colin J. Suckling, Carol Clements, Alan L. Harvey, William N. Hunter, Lindsay B. Tulloch
, Org. Biomol. Chem.
, 2009
, 7
, 1829
- Tandem ring-opening and formal [3 + 2] cycloaddition of furo[2,3-d]pyrimidine-2,4-diones. Li Huang, Ying Han, Jing Sun, Qiu Sun, Chao-Guo Yan
, Org. Biomol. Chem.
, 2023
, 21
, 6028
- Stereoselective synthesis of medicinally relevant furo[2,3-d]pyrimidine framework by thermal rearrangement of spirocyclic barbiturates. Anatoly N. Vereshchagin, Michail N. Elinson, Evgeniya O. Dorofeeva, Olga O. Sokolova, Ivan S. Bushmarinov, Michail P. Egorov
, RSC Adv.
, 2015
, 5
, 94986
- A review of the synthetic strategies toward spirobarbiturate-fused 3- to 7-membered rings. Akram Bagherinejad, Abdolali Alizadeh
, Org. Biomol. Chem.
, 2022
, 20
, 7188
- Identification of novel furo[2,3-d]pyrimidine based chalcones as potent anti-breast cancer agents: synthesis, in vitro and in vivo biological evaluation. Mai A. Mansour, Mamdouh A. Oraby, Zeinab A. Muhammad, Deena S. Lasheen, Hatem M. Gaber, Khaled A. M. Abouzid
, RSC Adv.
, 2022
, 12
, 8193
- Recent applications of barbituric acid in multicomponent reactions. Ghodsi Mohammadi Ziarani, Faezeh Aleali, Negar Lashgari
, RSC Adv.
, 2016
, 6
, 50895
- Pyrrolo-dC
oligonucleotides bearing alkynyl side chains with terminal triple bonds: synthesis, base pairing and fluorescent dye conjugates prepared by the azide–alkyne “click” reaction. Frank Seela, Venkata Ramana Sirivolu
, Org. Biomol. Chem.
, 2008
, 6
, 1674
- Aryl glyoxal: a prime synthetic equivalent for multicomponent reactions in the designing of oxygen heterocycles. Abdur Rehman Sheikh, Anam Arif, Md. Musawwer Khan
, RSC Adv.
, 2023
, 13
, 11652