The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
A New Condensation Reaction for the Synthesis of Carboxylic Esters from Nearly Equimolar Amounts of Carboxylic Acids and Alcohols Using 2-Methyl-6-nitrobenzoic Anhydride
Abstract
Various carboxylic esters were obtained in excellent yields with high chemoselectivities from nearly equimolar amounts of carboxylic acids and alcohols using 2-methyl-6-nitrobenzoic anhydride with triethylamine in the presence of a catalytic amount of 4-(dimethylamino)pyridine.
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Citations
Cites
Manabe, K., Sun, X.-M., & Kobayashi, S. (2001) · Journal of the American Chemical Society · doi:10.1021/ja016338q · Cited by 215
Cited by
Shiina, I. (2007) · Chemical Reviews · doi:10.1021/cr050045o · Cited by 346
Self-citationYamashita, K., Okuyama, M., Nakagawa, R., Honma, S., Satoh, F., Morimoto, R., Ito, S., Takahashi, M., & Numazawa, M. (2008) · Journal of Chromatography A · doi:10.1016/j.chroma.2008.05.034 · Cited by 57
Metadata
- Authors
- Shiina, I., Ibuka, R., & Kubota, M.
- Venue
- Chemistry Letters
- Publisher
- Oxford University Press (OUP)
- Published
- 2002-03-01
- Volume
- 31
- Issue
- 3
- Pages
- 286-287
- ISSN
- 0366-7022 (ISSN-L)
- 1348-0715
- OpenAlex
- W2041084364
- Cited by
- 193
- References
- 1
- FWCI
- 3.67
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: A New Condensation Reaction for the Synthesis of Carboxylic Esters from Nearly Equimolar Amounts of Carboxylic Acids and Alcohols Using 2-Methyl-6-nitrobenzoic Anhydride. https://app.cochat.ai/papers/10.1246/cl.2002.286
- The paper
- Shiina, I., Ibuka, R., & Kubota, M. (2002). A New Condensation Reaction for the Synthesis of Carboxylic Esters from Nearly Equimolar Amounts of Carboxylic Acids and Alcohols Using 2-Methyl-6-nitrobenzoic Anhydride. Chemistry Letters. https://doi.org/10.1246/cl.2002.286
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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
