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Halogenated indoles eradicate bacterial persister cells and biofilms
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AMB Express
[DOI: 10.1186/s13568-016-0297-6]
Joule, J. A., Science of Synthesis, (2001) 10, 428..
From o-Alkynylarylamines
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Science of Synthesis
Joule, J. A., Science of Synthesis, (2001) 10, 421..
From 2-(o-Nitroaryl)enamines; Leimgruber–Batcho Synthesis
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Science of Synthesis
Joule, J. A., Science of Synthesis, (2001) 10, 548..
Giving C-Lithium Indoles
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Science of Synthesis
Joule, J. A., Science of Synthesis, (2001) 10, 384..
From ortho-Substituted Nitroarenes; Bartoli Synthesis
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Science of Synthesis
Gribble, G. W., Science of Synthesis, (2006) 8, 389..
By Halogen–Lithium Exchange
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Science of Synthesis
Westbrook, J. A.; Schaus, S. E., Science of Synthesis, (2007) 20, 1103..
Addition of Organometallic Reagents to Oxalates
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Science of Synthesis
Appukkuttan, Prasad; Van der Eycken, Erik; Dehaen, Wim, Synlett 2005, 127-133.
Microwave-Enhanced Cadogan Cyclization: An Easy Access to the 2-Substituted Carbazoles and other Fused Heterocyclic Systems
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Synlett
[DOI: 10.1055/s-2004-836030]
Zhdankin, V. V., Science of Synthesis Knowledge Updates, (2015) 1, 260..
Alkynylation Using 1-Alkynylbenziodoxoles
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Science of Synthesis
Colobert, F.; Leroux, F. R., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 1, 359..
With Aryl and Hetaryl Halides or Aryl Trifluoromethanesulfonates
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Science of Synthesis
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