The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
The utilization of spirocyclic scaffolds in novel drug discovery
Open accessAbstract
Spirocycles are ring systems in which two rings are fused through a single atom, referred to as the spiro atom. The ethylene glycol ketal of cyclohexanone is an example of a well-known type of spir...
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The use of spirocyclic scaffolds in drug discovery
Zheng, Y., Tice, C. M., & Singh, S. B. (2014) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2014.06.081 · Cited by 1,036
Self-citationRitchie, T. J., & Macdonald, S. J. F. (2009) · Drug Discovery Today · doi:10.1016/j.drudis.2009.07.014 · Cited by 901
Four-Membered Ring-Containing Spirocycles: Synthetic Strategies and Opportunities
Carreira, E. M., & Fessard, T. C. (2014) · Chemical Reviews · doi:10.1021/cr500127b · Cited by 630
Heteroaromatic Rings of the Future
Pitt, W. R., Parry, D. M., Perry, B. G., & Groom, C. R. (2009) · Journal of Medicinal Chemistry · doi:10.1021/jm801513z · Cited by 332
Wang, S., Sun, W., Zhao, Y., McEachern, D., Meaux, I., Barrière, C., Stuckey, J. A., Meagher, J. L., Bai, L., Liu, L., et al. (2014) · Cancer Research · doi:10.1158/0008-5472.can-14-0799 · Cited by 328
Patchett, A. A., Nargund, R. P., Tata, J. R., Chen, M. H., Barakat, K. J., Johnston, D. B., Cheng, K., Chan, W. W., Butler, B., & Hickey, G. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.15.7001 · Cited by 327
Chapter 26. Privileged structures — An update
Patchett, A. A., & Nargund, R. P. (2000) · Annual Reports in Medicinal Chemistry · doi:10.1016/s0065-7743(00)35027-8 · Cited by 302
Link, J. O., Taylor, J. G., Xu, L., Mitchell, M., Guo, H., Liu, H., Kato, D., Kirschberg, T., Sun, J., Squires, N., et al. (2014) · Journal of Medicinal Chemistry · doi:10.1021/jm401499g · Cited by 295
A Library of Spirooxindoles Based on a Stereoselective Three-Component Coupling Reaction
Lo, M. M.-C., Neumann, C. S., Nagayama, S., Perlstein, E. O., & Schreiber, S. L. (2004) · Journal of the American Chemical Society · doi:10.1021/ja045089d · Cited by 276
Ohtake, Y., Sato, T., Kobayashi, T., Nishimoto, M., Taka, N., Takano, K., Yamamoto, K., Ohmori, M., Yamaguchi, M., Takami, K., et al. (2012) · Journal of Medicinal Chemistry · doi:10.1021/jm300884k · Cited by 174
Metadata
- Authors
- Zheng, Y.-J., & Tice, C. M.
- Venue
- Expert Opinion on Drug Discovery
- Publisher
- Informa UK Limited
- Published
- 2016-06-09
- Volume
- 11
- Issue
- 9
- Pages
- 831-834
- ISSN
- 1746-0441 (ISSN-L)
- 1746-045X
- OpenAlex
- W2401558437
- Cited by
- 299
- References
- 24
- Type
- journal article
- Language
- en
- Open access
- bronze
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.