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- Selective reduction of ketones using water as a hydrogen source under high hydrostatic pressure. Anna Tomin, Alexander Lazarev, Matthew P. Bere, Hana Redjeb, Béla Török
, Org. Biomol. Chem.
, 2012
, 10
, 7321
- Unprecedented thiocarbamidation of nitroarenes: a facile one-pot route to unsymmetrical thioureas. Soumya Dutta, Manas Mondal, Tubai Ghosh, Amit Saha
, Org. Chem. Front.
, 2019
, 6
, 70
- 438. Bromination and nitration of 5-hydroxyflavone. P. E. McCusker, Eva M. Philbin, T. S. Wheeler
, J. Chem. Soc.
, 1963
, 2374
- β-Cyclodextrin–TiO2: Green Nest for reduction of nitroaromatic compounds. Mazaher Abdollahi Kakroudi, Foad Kazemi, Babak Kaboudin
, RSC Adv.
, 2014
, 4
, 52762
- Differences in the selective reduction mechanism of 4-nitroacetophenone catalysed by rutile- and anatase-supported ruthenium catalysts. Jin Zhang, Linjuan Pei, Jie Wang, Pengqi Zhu, Xianmo Gu, Zhanfeng Zheng
, Catal. Sci. Technol.
, 2020
, 10
, 1518
- Reactions of 1-aryl-2,2-dihalogenoethanone oximes with tetrasulfur tetranitride (S4N4): a general method for the synthesis of 3-aryl-4-halogeno-1,2,5-thiadiazoles. Sung Cheol Yoon, Jaeeock Cho, Kyongtae Kim
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 109
- CCCXXVII.—Benzaldehyde-p-arsonic acid of acylphenylketones and their derivatives. Chemotherapeutic examination of these and other arsonic acids. Charles Stanley Gibson, Barnett Levin
, J. Chem. Soc.
, 1931
, 2388
- Cinnolines. Part II. Reaction with hydrogen peroxide and acetic acid. M. H. Palmer, E. R. R. Russell
, J. Chem. Soc. C
, 1968
, 2621
- A novel acid-catalyzed rearrangement of 2-substituted-3-(2-nitrophenyl)oxiranes for the synthesis of di- and mono-oxalamides. Vakhid A. Mamedov, Vera L. Mamedova, Gul'nas Z. Khikmatova, Ekaterina V. Mironova, Dmitry B. Krivolapov, Olga B. Bazanova, Denis V. Chachkov, Sergey A. Katsyuba, Il'dar Kh Rizvanov, Shamil K. Latypov
, RSC Adv.
, 2016
, 6
, 27885
- A simple approach to pyrrolylimidazole derivatives by azirine ring expansion with imidazolium ylides. Alexander F. Khlebnikov, Olesya A. Tomashenko, Liya D. Funt, Mikhail S. Novikov
, Org. Biomol. Chem.
, 2014
, 12
, 6598