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- Synthesis and characterization of a novel Fe3O4@SiO2–BenzIm-Fc[Cl]/BiOCl nano-composite and its efficient catalytic activity in the ultrasound-assisted synthesis of diverse chromene analogs. Reza Mohammadi, Somayeh Esmati, Mahdi Gholamhosseini-Nazari, Reza Teimuri-Mofrad
, New J. Chem.
, 2019
, 43
, 135
- Development and applications of a near-infrared dye–benzylguanine conjugate to specifically label SNAP-tagged proteins. Xinbo Song, Hui Bian, Chao Wang, Mingyu Hu, Ning Li, Yi Xiao
, Org. Biomol. Chem.
, 2017
, 15
, 8091
- Enantioselective synthesis of 4-aryl-3,4-dihydrocoumarins via N-heterocyclic carbene catalyzed β-arylation/cyclization of α-bromoenals. Yu-Jing Liang, Yuan-Yuan Gao, Hua-Bo Han, Lu Li, Lantao Liu
, Org. Biomol. Chem.
, 2024
- Chiral phosphoric acid-catalysed Friedel–Crafts alkylation reaction of indoles with racemic spiro indolin-3-ones. Qin Yin, Shu-Li You
, Chem. Sci.
, 2011
, 2
, 1344
- 45. Investigations on the influence of chemical constitution upon toxicity. Part II. Compounds related to “prostigmine”. Robert D. Haworth, Alex. H. Lamberton, David Woodcock
, J. Chem. Soc.
, 1947
, 182
- Synthesis and characterisation of pure isomers of iodoacetamidotetramethylrhodamine. John E. T. Corrie, James S. Craik
, J. Chem. Soc., Perkin Trans. 1
, 1994
, 2967
- Protein-specific localization of a rhodamine-based calcium-sensor in living cells. Marcel Best, Isabel Porth, Sebastian Hauke, Felix Braun, Dirk-Peter Herten, Richard Wombacher
, Org. Biomol. Chem.
, 2016
, 14
, 5606
- Fabrication of chemically and in situ modified carbon paste electrodes for the potentiometric determination of chlorpromazine HCl in pure pharmaceutical preparations, urine and serum. Gehad G. Mohamed, Eman Y. Z. Frag, M. A. Zayed, M. M. Omar, Sally E. A. Elashery
, New J. Chem.
, 2017
, 41
, 15612
-
Palladium
catalytic system for inhibition of
O-arylation type reaction and regioselective direct arylation at C2 of phenols. Kassem Beydoun, Henri Doucet
, Catal. Sci. Technol.
, 2011
, 1
, 1243
- Tris-hydroxymethylaminomethane (THAM): a novel organocatalyst for a environmentally benign synthesis of medicinally important tetrahydrobenzo[b]pyrans and pyran-annulated heterocycles. Kapil S. Pandit, Pramod V. Chavan, Uday V. Desai, Makarand A. Kulkarni, Prakash P. Wadgaonkar
, New J. Chem.
, 2015
, 39
, 4452