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- Kinetic evidence for the occurrence of a stepwise mechanism in the aminolysis of N-ethoxycarbonylphthalimide. Mohammad Niyaz Khan
, J. Chem. Soc., Perkin Trans. 2
, 1988
, 1129
- Oxidative desulfurization–fluorination of thioethers. Application for the synthesis of fluorinated nitrogen containing building blocks. Verena Hugenberg, Roland Fröhlich, Günter Haufe
, Org. Biomol. Chem.
, 2010
, 8
, 5682
- Catalytic hydrogenations of cyclic imides and ayhydrides. A. J. McAlees, R. McCrindle
, J. Chem. Soc. C
, 1969
, 2425
- Studies in sigmatropic rearrangements of N-prenylindole derivatives – a formal enantiomerically pure synthesis of tryprostatin B. A. Sofia P. Cardoso, M. Manuel B. Marques, Natarajan Srinivasan, Sundaresan Prabhakar, Ana M. Lobo, Henry S. Rzepa
, Org. Biomol. Chem.
, 2006
, 4
, 3966
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Stereoselective benzylic α-acylamino radical cyclisation: a model
study for the Tacaman indole alkaloid skeleton. Rainer Clauss, Roger Hunter
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 71
- Regioselective solid-phase synthesis of N-mono-hydroxylated and N-mono-methylated acylpolyamine spider toxins using an 2-(ortho-nitrophenyl)ethanal-modified resin. Denise Pauli, Stefan Bienz
, Org. Biomol. Chem.
, 2015
, 13
, 4473
- Chiral sensors for determining the absolute configurations of α-amino acid derivatives. Zhongxiang Chen, Hongjun Fan, Shiwei Yang, Guangling Bian, Ling Song
, Org. Biomol. Chem.
, 2018
, 16
, 8311
- Kinetics and mechanism of aminolysis of phthalimide and N-substituted phthalimides. Evidence for the occurrence of intramolecular general acid-base catalysis in the reactions of ionized phthalimides with primary amines. Mohammad Niyaz Khan
, J. Chem. Soc., Perkin Trans. 2
, 1990
, 435
- Index pages
, J. Chem. Soc., Perkin Trans. 2
, 1988
, A001
- Studies related to penicillins. Part VII. The structure of the epimers derived from 6β-substituted penicillanic acids. J. R. Jackson, R. J. Stoodley
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 895