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- Single and double intramolecular proton transfers in the electronically excited state of flavone derivatives. I. E. Serdiuk, A. D. Roshal
, RSC Adv.
, 2015
, 5
, 102191
- Association thermodynamic parameters for nano Cu(NO3)2·2.5H2O with ligands at different temperatures. Sameh G. Sanad, Magdy Shebl
, RSC Adv.
, 2022
, 12
, 28902
- New iron(iii) complex of bis-bidentate-anchored diacyl resorcinol on a Fe3O4 nanomagnet: C–H bond oxygenation, oxidative cleavage of alkenes and benzoxazole synthesis . Mona Majedi, Elham Safaei, Sašo Gyergyek
, RSC Adv.
, 2023
, 13
, 4040
- Spirochromone-chalcone conjugates as antitubercular agents: synthesis, bio evaluation and molecular modeling studies. M. Mujahid, P. Yogeeswari, D. Sriram, U. M. V. Basavanag, Erik Díaz-Cervantes, Luis Córdoba-Bahena, Juvencio Robles, R. G. Gonnade, M. Karthikeyan, Renu Vyas, M. Muthukrishnan
, RSC Adv.
, 2015
, 5
, 106448
- Nucleophilic substitution reaction as an important tool in the synthetic protocol for selenium donor containing Schiff bases: applications of metal complexes in homogeneous catalysis. Anupma Tyagi, Suraj Purohit, Preeti Oswal, Saumya Rawat, Varsha Negi, Ajai K. Singh, Arun Kumar
, New J. Chem.
, 2023
, 47
, 12511
- Thermal Claisen rearrangement studies on 4,6- and 2,4-diacetylresorcinol bisallyl ethers: observation of loss or [1,5] sigmatropic shift of acetyl groups. Ammanamanchi S. R. Anjaneyulu, Uppuluri V. Mallavadhani
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 623
- 369. A new factor controlling certain chelations, with special reference to disubstitution in the resorcinol nucleus. Wilson Baker
, J. Chem. Soc.
, 1934
, 1684
- 383. Thermal cyclization of o-aroyloxyacetoarones. Part II. Further syntheses in the flavone series (diflavones and flavonols). H. M. Lynch, T. M. O'Toole, T. S. Wheeler
, J. Chem. Soc.
, 1952
, 2063
- 249. Usnic acid. Part VIII. C-diacetyl derivatives of phloroglucinol and C-methylphloroglucinol. F. M. Dean, Alexander Robertson
, J. Chem. Soc.
, 1953
, 1241
- 21. 4 : 6- and 2 : 4-Diacetylresorcinol. Wilson Baker
, J. Chem. Soc.
, 1934
, 71