The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.
Fascinating frontiers of N/O-functionalized N-heterocyclic carbene chemistry: from chemical catalysis to biomedical applications
Abstract
The in vogue N-heterocyclic carbenes (NHCs) have attracted attention largely for its new found popularity in chemical catalysis and also for displaying promising traits in biomedical applications. The current perspective provides an account of our efforts in exploring the utility of N/O-functionalized N-heterocyclic carbenes in these two areas. On the catalysis front, we have employed the N/O-functionalized N-heterocyclic carbene based precatalysts for the C-C and C-N bond forming reactions like the Suzuki-Miyaura, Sonogashira and Hiyama cross-couplings, the base-free Michael addition, the alkene and alkyne hydroamination reactions and the ring-opening polymerization (ROP) of L-lactides that produce biodegradable polylactide polymers while on the biomedical application front, the anticancer and antimicrobial properties of these N/O-functionalized N-heterocyclic carbene complexes were evaluated. Towards this objective, the N-heterocyclic carbene chemistry of a variety of transition metals like Ag, Au, Ni and Pd has been investigated.
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Cites
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Polymerization of Lactide with Zinc and Magnesium β-Diiminate Complexes: Stereocontrol and Mechanism
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Polymerization of lactide and related cyclic esters by discrete metal complexes
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Lewis acid catalyzed polymerization of L-lactide. Kinetics and mechanism of the bulk polymerization
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Syntheses and application of polylactides
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Cited by
Recent advances in Sonogashira reactions
Chinchilla, R., & Nájera, C. (2011) · Chemical Society Reviews · doi:10.1039/c1cs15071e · Cited by 1,541
Fortman, G. C., & Nolan, S. P. (2011) · Chemical Society Reviews · doi:10.1039/c1cs15088j · Cited by 1,258
Stephen, R., Sunoj, R. B., & Ghosh, P. (2011) · Dalton Transactions · doi:10.1039/c1dt10345h · Cited by 23
Self-citation
Metadata
- Authors
- John, A., & Ghosh, P.
- Venue
- Dalton Transactions
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2010
- Volume
- 39
- Issue
- 31
- Pages
- 7183
- ISSN
- 1477-9226 (ISSN-L)
- 1477-9234
- OpenAlex
- W1963539860
- Cited by
- 185
- References
- 8
- FWCI
- 9.63
- Type
- journal article
- Language
- en
- Open access
- closed
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