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- Peroxidatic activity of haem octapeptide complexes with anilines, naphthols and phenols. Ian D. Cunningham, John L. Bachelor, John M. Pratt
, J. Chem. Soc., Perkin Trans. 2
, 1994
, 1347
- Molecular and intramolecular relaxation in some substituted anilines. N. K. Mehrotra, T. C. Pant, M. C. Saxena
, Trans. Faraday Soc.
, 1969
, 65
, 2078
- Sulphuryl chloride as an electrophile. Part II. Substituted m-di-methoxybenzenes. R. Bolton
, J. Chem. Soc. B
, 1968
, 712
- Self-optimisation of the final stage in the synthesis of EGFR kinase inhibitor AZD9291 using an automated flow reactor. Nicholas Holmes, Geoffrey R. Akien, A. John Blacker, Robert L. Woodward, Rebecca E. Meadows, Richard A. Bourne
, React. Chem. Eng.
, 2016
, 1
, 366
- Kinetic study of the fast thermal
cis-to-trans
isomerisation of para-, ortho- and polyhydroxyazobenzenes. Jaume Garcia-Amorós, Antoni Sánchez-Ferrer, Walter A. Massad, Santi Nonell, Dolores Velasco
, Phys. Chem. Chem. Phys.
, 2010
, 12
, 13238
- Aryllead triacetates: regioselective reagents for N-arylation of amines. Derek H. R. Barton, Dervilla M. X. Donnelly, Jean-Pierre Finet, Patrick J. Guiry
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 2095
- Quinoline alkaloids. Part 20. Synthesis of ptelefolone and O-methylribaline. Ring closure of epoxides of 3-prenylquinolones. John L. Gaston, Michael F. Grundon
, J. Chem. Soc., Perkin Trans. 1
, 1980
, 2294
- Anticancer potential of novel symmetrical and asymmetrical dihydropyridines against breast cancer via EGFR inhibition: molecular design, synthesis, analysis and screening. Syed Faizan, Sirajunisa Talath, Adil Farooq Wali, Umme Hani, Nazima Haider, Subhankar P. Mandal, B. R. Prashantha Kumar
, RSC Adv.
, 2024
, 14
, 11368
- Chiral ionic Brønsted acid–achiral Brønsted base synergistic catalysis for asymmetric sulfa-Michael addition to nitroolefins. Daisuke Uraguchi, Natsuko Kinoshita, Daisuke Nakashima, Takashi Ooi
, Chem. Sci.
, 2012
, 3
, 3161
- Precipitation-driven self-sorting of imines. Rio Carlo Lirag, Karolina Osowska, Ognjen Š. Miljanić
, Org. Biomol. Chem.
, 2012
, 10
, 4847