The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Nickel‐Catalyzed Barton Decarboxylation and Giese Reactions: A Practical Take on Classic Transforms
Open accessAbstract
Two named reactions of fundamental importance and paramount utility in organic synthesis have been reinvestigated, the Barton decarboxylation and Giese radical conjugate addition. N‐hydroxyphthalimide (NHPI) based redox‐active esters were found to be convenient starting materials for simple, thermal, Ni‐catalyzed radical formation and subsequent trapping with either a hydrogen atom source (PhSiH 3) or an electron‐deficient olefin. These reactions feature operational simplicity, inexpensive reagents, and enhanced scope as evidenced by examples in the realm of peptide chemistry.
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Cites
Contemporary strategies for peptide macrocyclization
White, C. J., & Yudin, A. K. (2011) · Nature Chemistry · doi:10.1038/nchem.1062 · Cited by 1,088
Radical chemistry associated with the thiocarbonyl group
Crich, D., & Quintero, L. (1989) · Chemical Reviews · doi:10.1021/cr00097a001 · Cited by 496
A chemical biology route to site-specific authentic protein modifications
Yang, A., Ha, S., Ahn, J., Kim, R., Kim, S., Lee, Y., Kim, J., Söll, D., Lee, H.-Y., & Park, H.-S. (2016) · Science · doi:10.1126/science.aah4428 · Cited by 232
Cited by
Residue-Specific Peptide Modification: A Chemist’s Guide
deGruyter, J. N., Malins, L. R., & Baran, P. S. (2017) · Biochemistry · doi:10.1021/acs.biochem.7b00536 · Cited by 573
Self-citationDecarboxylative reactions with and without light – a comparison
Schwarz, J., & König, B. (2018) · Green Chemistry · doi:10.1039/c7gc02949g · Cited by 431
Desulfonylation via Radical Process: Recent Developments in Organic Synthesis
Chu, X.-Q., Ge, D., Cui, Y.-Y., Shen, Z.-L., & Li, C.-J. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00084 · Cited by 259
Direct decarboxylative Giese reactions
Kitcatt, D. M., Nicolle, S., & Lee, A.-L. (2022) · Chemical Society Reviews · doi:10.1039/d1cs01168e · Cited by 257
Modular, stereocontrolled C β –H/C α –C activation of alkyl carboxylic acids
Shang, M., Feu, K. S., Vantourout, J. C., Barton, L. M., Osswald, H. L., Kato, N., Gagaring, K., McNamara, C. W., Chen, G., Hu, L., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1903048116 · Cited by 53
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Metadata
- Authors
- Qin, T., Malins, L. R., Edwards, J. T., Merchant, R. R., Novak, A. J. E., Zhong, J. Z., Mills, R. B., Yan, M., Yuan, C., Eastgate, M. D., & Baran, P. S.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2016-12-16
- Volume
- 56
- Issue
- 1
- Pages
- 260-265
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2561830131
- Cited by
- 303
- References
- 3
- FWCI
- 15.44
- Type
- journal article
- Language
- en
- Open access
- green
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- Qin, T., Malins, L. R., Edwards, J. T., Merchant, R. R., Novak, A. J. E., Zhong, J. Z., Mills, R. B., Yan, M., Yuan, C., Eastgate, M. D., & Baran, P. S. (2017). Nickel‐Catalyzed Barton Decarboxylation and Giese Reactions: A Practical Take on Classic Transforms. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201609662
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