The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.
Silver‐Catalyzed Isocyanide‐Alkyne Cycloaddition: A General and Practical Method to Oligosubstituted Pyrroles
Abstract
Ag2CO3 is the key: The transition-metal-catalyzed cycloaddition of isocyanides and unactivated terminal alkynes has been realized with Ag2CO3 as a unique and robust catalyst (see scheme). The protocol is highly efficient, allowing a broad range of terminal and internal alkynes to react under base- and ligand-free conditions, generating synthetically useful oligosubstituted pyrroles in high yields.
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Cites
Coinage Metal-Assisted Synthesis of Heterocycles
Patil, N. T., & Yamamoto, Y. (2008) · Chemical Reviews · doi:10.1021/cr050041j · Cited by 1,188
Lamellarins and Related Pyrrole-Derived Alkaloids from Marine Organisms
Fan, H., Peng, J., Hamann, M. T., & Hu, J.-F. (2008) · Chemical Reviews · doi:10.1021/cr078199m · Cited by 1,060
Bellina, F., & Rossi, R. (2006) · Tetrahedron · doi:10.1016/j.tet.2006.05.024 · Cited by 606
Biological formation of pyrroles: Nature's logic and enzymatic machinery
Walsh, C. T., Garneau‐Tsodikova, S., & Howard‐Jones, A. R. (2006) · Natural Product Reports · doi:10.1039/b605245m · Cited by 445
Larionov, O. V., & de Meijere, A. (2005) · Angewandte Chemie International Edition · doi:10.1002/anie.200502140 · Cited by 231
Oligosubstituted Pyrroles Directly from Substituted Methyl Isocyanides and Acetylenes
Lygin, A. V., Larionov, O. V., Korotkov, V. S., & de Meijere, A. (2008) · Chemistry - A European Journal · doi:10.1002/chem.200801395 · Cited by 108
Ito, S., Wakamatsu, K., Glass, K. E., & Simon, J. D. (2012) · Analytical Biochemistry · doi:10.1016/j.ab.2012.12.005 · Cited by 58
Larionov, O. V., & de Meijere, A. (2005) · Angewandte Chemie · doi:10.1002/ange.200502140 · Cited by 58
Kelly, A. R., Kerrigan, M. H., & Walsh, P. J. (2008) · Journal of the American Chemical Society · doi:10.1021/ja710988q · Cited by 48
Antiinflammatory 4,5-Diarylpyrroles: Synthesis and QSAR
Wilkerson, W. W., Galbraith, W., Gans-Brangs, K. R., Grubb, M. F., Hewes, W. E., JAFFEE, B. D., Kenney, J., Kerr, J., & Wong, N. (1994) · Journal of Medicinal Chemistry · doi:10.1021/jm00033a017 · Cited by 42
Cited by
Xu, S., Liu, J., Hu, D., & Bi, X. (2015) · Green Chemistry · doi:10.1039/c4gc01328j · Cited by 91
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Metadata
- Authors
- Liu, J., Fang, Z., Zhang, Q., Liu, Q., & Bi, X.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2013-05-06
- Volume
- 52
- Issue
- 27
- Pages
- 6953-6957
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2165742515
- Cited by
- 299
- References
- 11
- FWCI
- 19.13
- Type
- journal article
- Language
- en
- Open access
- closed
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- Liu, J., Fang, Z., Zhang, Q., Liu, Q., & Bi, X. (2013). Silver‐Catalyzed Isocyanide‐Alkyne Cycloaddition: A General and Practical Method to Oligosubstituted Pyrroles. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201302024
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