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- A radical based addition–elimination route for the preparation of indoles. John A. Murphy, Karen A. Scott, Rhona S. Sinclair, Concepcion Gonzalez Martin, Alan R. Kennedy, Norman Lewis
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 2395
- Tetrathiafulvalene-mediated stereoselective synthesis of the tetracyclic core of Aspidosperma alkaloids. Rodney Fletcher, Murat Kizil, Christopher Lampard, John A. Murphy, Stephen J. Roome
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 2341
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Asymmetric dihydroxylation of allylic phosphine oxides
. Adam Nelson, Stuart Warren
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 2645
- A multivariate insight into ionic liquids toxicities. Alessio Paternò, Francesca D'Anna, Giuseppe Musumarra, Renato Noto, Salvatore Scirè
, RSC Adv.
, 2014
, 4
, 23985
- Structural study of three nimesulidetriazole derivatives using X-ray powder diffraction: effect of substitution on supramolecular assembly. Tanusri Dey, Soumen Ghosh, Jyoti Mareddy, Jayashree Anireddy, Sarbani Pal, Alok K. Mukherjee
, CrystEngComm
, 2015
, 17
, 764
- Structure-based design of 2,4-diaminopyrimidine derivatives bearing a pyrrolyl group as ALK and ROS1 inhibitors. Jie Wang, Shangfei Wei, Tong Li, Lingyun Xing, Meng Cao, Nan Jiang, Ming Guo, Daiying Zuo, Xin Zhai
, New J. Chem.
, 2020
, 44
, 5850
- Direct acylation of N-benzyltriflamides from the alcohol oxidation level via
palladium-catalyzed C–H bond activation. Jihye Park, Aejin Kim, Satyasheel Sharma, Minyoung Kim, Eonjeong Park, Yukyoung Jeon, Youngil Lee, Jong Hwan Kwak, Young Hoon Jung, In Su Kim
, Org. Biomol. Chem.
, 2013
, 11
, 2766
- Discovery of a novel binding pocket for CYP 2C9 inhibitors: crystallography, pharmacophore modelling and inhibitor SAR. Sarah E. Skerratt, Marcel J. de Groot, Chris Phillips
, Med. Chem. Commun.
, 2016
, 7
, 813
- An efficient protocol for Sharpless-style racemic dihydroxylation. Jason Eames, Helen J. Mitchell, Adam Nelson, Peter O’Brien, Stuart Warren, Paul Wyatt
, J. Chem. Soc., Perkin Trans. 1
, 1999
, 1095
- Synthesis of sulfonamide-based kinase inhibitors from sulfonates by exploiting the abrogated SN2 reactivity of 2,2,2-trifluoroethoxysulfonates. Christopher Wong, Roger J. Griffin, Ian R. Hardcastle, Julian S. Northen, Lan-Zhen Wang, Bernard T. Golding
, Org. Biomol. Chem.
, 2010
, 8
, 2457