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- Synthesis of tetraarylpyridines by chemo-selective Suzuki–Miyaura reactions of 3,5-dibromo-2,6-dichloropyridine. Sebastian Reimann, Silvio Parpart, Peter Ehlers, Muhammad Sharif, Anke Spannenberg, Peter Langer
, Org. Biomol. Chem.
, 2015
, 13
, 6832
- Sonogashira cross-coupling reactions of 3,5-dibromo-2,6-dichloropyridine. Sebastian Reimann, Peter Ehlers, Lars Ohlendorf, Peter Langer
, Org. Biomol. Chem.
, 2017
, 15
, 1510
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Catalytic asymmetric epoxidation with a chiral ruthenium porphyrin and
N-oxides
. Albrecht Berkessel, Matthias Frauenkron
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 2265
- Photoassisted oxygenation of alkane catalyzed by ruthenium complexes using 2,6-dichloropyridine N-oxide under visible light irradiation. Motowo Yamaguchi, Takashi Kumano, Dai Masui, Takamichi Yamagishi
, Chem. Commun.
, 2004
, 798
- Computationally designed tandem direct selective oxidation using molecular oxygen as oxidant without coreductant. Bo Yang, Thomas A. Manz
, RSC Adv.
, 2016
, 6
, 88189
- The mechanism of the electrophilic substitution of heteroaromatic compounds. Part VI. The nitration of pyridines in the 3-position as free bases and as conjugate acids. C. D. Johnson, A. R. Katritzky, B. J. Ridgewell, M. Viney
, J. Chem. Soc. B
, 1967
, 1204
- Regio- and stereo-selective oxidation of steroids using
2,6-dichloropyridine N-oxide catalysed by ruthenium
porphyrins. Tomoteru Shingaki, Keiko Miura, Tsunehiko Higuchi, Masaaki Hirobe, Tetsuo Nagano
, Chem. Commun.
, 1997
, 861
- The mechanism of the electrophilic substitution of heteroaromatic compounds. Part IX. General form of rate profiles for acid-catalysed hydrogen exchange as illustrated by substituted aminopyridines. G. P. Bean, C. D. Johnson, A. R. Katritzky, B. J. Ridgewell, A. M. White
, J. Chem. Soc. B
, 1967
, 1219
- Ru(ii) complexes with
N-heterocyclic carbene
ligands or terpyridine analogues: synthesis, characterization, and electrochemical and proton-dependent spectrometric properties. Hee-Jun Park, Young Keun Chung
, Dalton Trans.
, 2012
, 41
, 5678
- Inter- and intra-molecular C–H borylation for the formation of PAHs containing triarylborane and indole units. A. Escande, D. L. Crossley, J. Cid, I. A. Cade, I. Vitorica-Yrezabal, M. J. Ingleson
, Dalton Trans.
, 2016
, 45
, 17160