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- Halogenated semivolatile acetonitriles as chloramination disinfection by-products in water treatment: a new formation pathway from activated aromatic compounds. Kathryn L. Linge, Ina Kristiana, Deborah Liew, Adam Holman, Cynthia A. Joll
, Environ. Sci.: Processes Impacts
, 2020
, 22
, 653
- Radical fluoroalkylation reactions of (hetero)arenes and sulfides under red light photocatalysis. Damian E. Yerien, M. Victoria Cooke, M. Cecilia García Vior, Sebastián Barata-Vallejo, Al Postigo
, Org. Biomol. Chem.
, 2019
, 17
, 3741
- Synthesis of 3-substituted indoles via reactive alkylideneindolenine intermediates. Alessandro Palmieri, Marino Petrini, Rafik R. Shaikh
, Org. Biomol. Chem.
, 2010
, 8
, 1259
- 404. The alkaloids of Arundo donax L.. J. Madinaveitia
, J. Chem. Soc.
, 1937
, 1927
- Ru-catalysed C–H silylation of unprotected gramines, tryptamines and their congeners. K. Devaraj, C. Sollert, C. Juds, P. J. Gates, L. T. Pilarski
, Chem. Commun.
, 2016
, 52
, 5868
- Recent advances in the understanding of the interaction of antidepressant
drugs with serotonin and norepinephrine transporters. Jacob Andersen, Anders S. Kristensen, Benny Bang-Andersen, Kristian Strømgaard
, Chem. Commun.
, 2009
, 3677
- Molecular iodine mediated oxidative cleavage of the C–N bond of aryl and heteroaryl (dimethylamino)methyl groups into aldehydes. Ketan S. Mandrekar, Santosh G. Tilve
, New J. Chem.
, 2021
- Sn20(Si
t
Bu3)10Cl2 – the largest metalloid group 14 cluster shows a raspberry-like arrangement of smaller units. Mareike Binder, Claudio Schrenk, Andreas Schnepf
, Chem. Commun.
, 2019
, 55
, 12148
- High resolution X-ray and neutron diffraction studies on molecular complexes of chloranilic acid and lutidines. Ioana Sovago, Lynne H. Thomas, Martin S. Adam, Silvia C. Capelli, Chick C. Wilson, Louis J. Farrugia
, CrystEngComm
, 2016
, 18
, 5697
- Synthesis and evaluation of hybrid molecules targeting the vinca domain of tubulin. O. Gherbovet, Pedro A. Sánchez-Murcia, M. C. García Alvarez, J. Bignon, S. Thoret, F. Gago, F. Roussi
, Org. Biomol. Chem.
, 2015
, 13
, 3144