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, J. Chem. Soc.
, 1960
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- 151. Synthetic antimalarials. Part XIV. Some 2-arylamino-4-aminoalkylaminoquinazolines. F. H. S. Curd, J. K. Landquist, F. L. Rose
, J. Chem. Soc.
, 1947
, 775
- Reaction of quinazoline-2,4(1H,3H)-dione with N-substituted cyclic amines in combination with phosphoryl trichloride. Kenji Yoshida, Takashi Tanaka, Hiroshi Ohtaka
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 1279
- 357. Synthetic antimalarials. Part XXXII. Some 4-arylamino- and 4-arylthio-2-aminoalkylaminoquinazolines, and 2-arylthio-4-aminoalkylaminoquinazolines. F. H. S. Curd, E. Hoggarth, J. K. Landquist, F. L. Rose
, J. Chem. Soc.
, 1948
, 1766
- The design, synthesis and evaluation of selenium-containing 4-anilinoquinazoline hybrids as anticancer agents and a study of their mechanism. Baijiao An, Shun Zhang, Jinhui Hu, Tingting Pan, Ling Huang, Johnny Cheuk-on Tang, Xingshu Li, Albert S. C. Chan
, Org. Biomol. Chem.
, 2018
, 16
, 4701
- Nucleophile–nucleofuge duality of azide and arylthiolate groups in the synthesis of quinazoline and tetrazoloquinazoline derivatives. Andris Jeminejs, Irina Novosjolova, Ērika Bizdēna, Māris Turks
, Org. Biomol. Chem.
, 2021
, 19
, 7706
- A one-pot synthetic approach for the construction of a thiazolo[3,2-a]benzimidazole-linked quinazoline scaffold via palladium-catalyzed reactions. Ali Keivanloo, Atena Soozani, Mohammad Bakherad, Amir Hossein Amin
, Org. Chem. Front.
, 2018
, 5
, 1135
- Reaction of N-substituted cyclic amines with 2,4-dichloroquinazoline, 2,4-dichloropyrimidine, and its 5-methyl derivative. Kenji Yoshida, Masahiro Taguchi
, J. Chem. Soc., Perkin Trans. 1
, 1992
, 919
- Design, synthesis, and biological evaluation of novel bioactive thalidomide analogs as anticancer immunomodulatory agents. Anas Ramadan Kotb, Dina A. Bakhotmah, Abdallah E. Abdallah, Hazem Elkady, Mohammed S. Taghour, Ibrahim. H. Eissa, Mohamed Ayman El-Zahabi
, RSC Adv.
, 2022
, 12
, 33525
- Site-selective Suzuki–Miyaura coupling of heteroaryl halides – understanding the trends for pharmaceutically important classes. Joshua Almond-Thynne, David C. Blakemore, David C. Pryde, Alan C. Spivey
, Chem. Sci.
, 2017
, 8
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