The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Regioselective syntheses of fully-substituted 1,2,3-triazoles: the CuAAC/C–H bond functionalization nexus
Abstract
Regioselective syntheses of 1,4,5-trisubstituted 1,2,3-triazoles were accomplished by three different strategies, relying on (i) the interception of stoichiometrically formed 5-cuprated-1,2,3-triazoles, (ii) the use of stoichiometrically functionalized alkynes or (iii) catalytic C-H bond functionalizations. This perspective article summarizes progress in this research area until June 2010.
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Citations
Cites
Tornøe, C. W., Christensen, C., & Meldal, M. (2002) · The Journal of Organic Chemistry · doi:10.1021/jo011148j · Cited by 8,696
Cited by
Carboxylate-Assisted Ruthenium-Catalyzed Alkyne Annulations by C–H/Het–H Bond Functionalizations
Ackermann, L. (2014) · Accounts of Chemical Research · doi:10.1021/ar3002798 · Cited by 1,640
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Metadata
- Authors
- Ackermann, L., & Potukuchi, H. K.
- Venue
- Organic & Biomolecular Chemistry
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2010
- Volume
- 8
- Issue
- 20
- Pages
- 4503
- ISSN
- 1477-0520 (ISSN-L)
- 1477-0539
- OpenAlex
- W2078654359
- Cited by
- 246
- References
- 1
- FWCI
- 15.63
- Type
- journal article
- Language
- en
- Open access
- closed
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- Ackermann, L., & Potukuchi, H. K. (2010). Regioselective syntheses of fully-substituted 1,2,3-triazoles: the CuAAC/C–H bond functionalization nexus. Organic & Biomolecular Chemistry. https://doi.org/10.1039/c0ob00212g
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