The DOI matches its Crossref record.
Guanidines in Organic Synthesis
Abstract
Guanidine is categorized as an organic superbase, yet its synthetic application is immature despite its wide potential utility. The role of guanidine in organic synthesis, including asymmetric reactions, is discussed herein.
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Cited by
Carbon dioxide utilization with C–N bond formation: carbon dioxide capture and subsequent conversion
Yang, Z.-Z., He, L.-N., Gao, J., Liu, A.-H., & Yu, B. (2012) · Energy & Environmental Science · doi:10.1039/c2ee02774g · Cited by 520
Organocatalytic Asymmetric Epoxidation and Aziridination of Olefins and Their Synthetic Applications
Zhu, Y., Wang, Q., Cornwall, R. G., & Shi, Y. (2014) · Chemical Reviews · doi:10.1021/cr500064w · Cited by 512
Metadata
- Authors
- Ishikawa, T., & Kumamoto, T.
- Venue
- Synthesis
- Publisher
- Georg Thieme Verlag KG
- Published
- 2006
- Volume
- 2006
- Issue
- 05
- Pages
- 737-752
- ISSN
- 0039-7881 (ISSN-L)
- 1437-210X
- OpenAlex
- W2951021591
- Cited by
- 234
- References
- 0
- FWCI
- 7.38
- Type
- journal article
- Language
- de
- Open access
- closed
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- CoChat. (2026). Citation check: Guanidines in Organic Synthesis. https://app.cochat.ai/papers/10.1055/s-2006-926325
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- Ishikawa, T., & Kumamoto, T. (2006). Guanidines in Organic Synthesis. Synthesis. https://doi.org/10.1055/s-2006-926325
Data sources
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.
