Results
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Joule, J. A., Science of Synthesis, (2001) 10, 565..
Giving C-Halogen Indoles
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Science of Synthesis
Braverman, S.; Cherkinsky, M.; Birsa, M. L., Science of Synthesis, (2005) 18, 72..
Carbon Dioxide as Protecting and Activating Group
,
Science of Synthesis
Joule, J. A., Science of Synthesis, (2001) 10, 591..
Of C-Halogen Indoles
,
Science of Synthesis
Gribble, G. W., Science of Synthesis, (2006) 8, 389..
By Halogen–Lithium Exchange
,
Science of Synthesis
Benneche, T., Science of Synthesis, (2007) 29, 173..
Formation of α-Alkoxy Nitrogen Compounds
,
Science of Synthesis
Rossi, Elisabetta; Abbiati, Giorgio; Canevari, Valentina; Celentano, Giuseppe; Magri, Elsa, Synthesis 2006, 299-304.
2-Trifluoromethanesulfonyloxyindole-1-carboxylic Acid Ethyl Ester: A Practical Intermediate for the Synthesis of 2-Carbosubstituted Indoles
,
Synthesis
[DOI: 10.1055/s-2005-918509]
Ila, Hiriyakkanavar; Markiewicz, John T.; Malakhov, Vladimir; Knochel, Paul, Synthesis 2013, 45, 2343-2371.
Metalated Indoles, Indazoles, Benzimidazoles, and Azaindoles and Their Synthetic Applications
,
Synthesis
[DOI: 10.1055/s-0033-1338501]
Joule, J. A., Science of Synthesis Knowledge Updates, (2010) 2, 350..
Giving C-Halogen Indoles
,
Science of Synthesis
Joule, J. A., Science of Synthesis Knowledge Updates, (2010) 2, 390..
Modification of N-Sulfur Functionality
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Science of Synthesis