The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.
Applications of Multicomponent Reactions to the Synthesis of Diverse Heterocyclic Scaffolds
Open accessAbstract
The sequencing of multicomponent reactions (MCRs) and subsequent cyclization reactions is a powerful stratagem for the rapid synthesis of diverse heterocyclic scaffolds. The optimal MCR is sufficiently flexible that it can be employed to generate adducts bearing a variety of functional groups that may then be selectively paired to enable different cyclization manifolds, thereby leading to a diverse collection of products. The growing interest in diversity‐oriented synthesis has led to increased attention to this paradigm for library synthesis, which has inspired many advances in the design and implementation of MCRs for the construction of diverse heterocyclic scaffolds.
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Cites
Recent Developments in Isocyanide Based Multicomponent Reactions in Applied Chemistry
Dömling, A. (2006) · Chemical Reviews · doi:10.1021/cr0505728 · Cited by 4,106
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The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged Substructures
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A Planning Strategy for Diversity‐Oriented Synthesis
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Diversity-oriented synthesis: Exploring the intersections between chemistry and biology
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Towards the Optimal Screening Collection: A Synthesis Strategy
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Chemistry, Biology, and Medicinal Potential of Narciclasine and its Congeners
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Cited by
Multicomponent reactions for the synthesis of pyrroles
Estévez, V., Villacampa, M., & Menéndez, J. C. (2010) · Chemical Society Reviews · doi:10.1039/b917644f · Cited by 744
Metadata
- Authors
- Sunderhaus, J. D., & Martin, S. F.
- Venue
- Chemistry – A European Journal
- Publisher
- Wiley
- Published
- 2009-01-20
- Volume
- 15
- Issue
- 6
- Pages
- 1300-1308
- ISSN
- 0947-6539 (ISSN-L)
- 1521-3765
- OpenAlex
- W2162083881
- Cited by
- 745
- References
- 18
- FWCI
- 27.46
- Type
- journal article
- Language
- en
- Open access
- bronze
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