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- MRI ParaCEST agents that improve amide based pH measurements by limiting inner sphere water T2 exchange. Mark Milne, Melissa Lewis, Nevin McVicar, Mojmir Suchy, Robert Bartha, Robert H. E. Hudson
, RSC Adv.
, 2014
, 4
, 1666
- Sulfur-mediated synthesis of unsymmetrically substituted N-aryl oxalamides by the cascade thioamidation/cyclocondensation and hydrolysis reaction. Tatyana A. Tikhonova, Nikita V. Ilment, Konstantin A. Lyssenko, Igor V. Zavarzin, Yulia A. Volkova
, Org. Biomol. Chem.
, 2020
, 18
, 5050
- Three-step synthesis of 2,5,7-trisubstituted indoles from N-acetyl-2,4,6-trichloroaniline using Pd-catalyzed site-selective cross-coupling. Miyuki Yamaguchi, Kei Manabe
, Org. Biomol. Chem.
, 2017
, 15
, 6645
- CLXIII.—Primary interaction of chlorine and acetanilides. Kennedy Joseph Previté Orton, William Jacob Jones
, J. Chem. Soc., Trans.
, 1909
, 95
, 1456
- CXXVIII.—A method of chlorination. Chlorination of anilines and phenols. Kennedy Joseph Previté Orton, Harold King
, J. Chem. Soc., Trans.
, 1911
, 99
, 1185
- Some observations relating to substituent effects in halogenation. Part II. The reaction of m- and p-chloroacetanilide with chlorine in acetic acid. O. M. H. el Dusouqui, M. Hassan
, J. Chem. Soc. B
, 1966
, 374
- XLIX.—The action of acetylchloro- and acetylbromo-aminobenzenes on amines and phenylhydrazine. F. D. Chattaway, K. J. P. Orton
, J. Chem. Soc., Trans.
, 1901
, 79
, 461
- CLIV.—The relation of the velocity of chlorination of aromatic compounds to constitution. Part I. Chlorination of anilides. Kennedy Joseph Previté Orton, Harold King
, J. Chem. Soc., Trans.
, 1911
, 99
, 1369
- Some observations relating to substituent effects in halogenation. Part VI. Kinetics and products of the reaction of 2-chloroacetanilide with chlorine in acetic acid. O. M. H. el Dusouqui, M. Hassan, B. Ibrahim
, J. Chem. Soc. B
, 1970
, 926
- Molecular rearrangements. Part VIII. The influence of nuclear substituents on the rearrangement of N-chloroacetanilides. I. M. Abdel Rahman, W. J. Hickinbottom, S. Wasif
, J. Chem. Soc. B
, 1970
, 1128