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The Nitro Group in Organic Synthesis
Abstract
The most useful reactions of organonitro compounds in organic synthesis Compounds containing nitro groups are useful intermediates for the synthesis of natural products and other complex organic molecules. The Nitro Group in Organic Synthesis focuses on reactions that proceed under mild conditions, important functional groups that can be synthesized by conversion of nitro groups, and the stereoselectivity of reactions of nitro compounds. These issues are of great importance to practicing researchers in today's pharmaceutical, agrochemical, and fine chemical industries. The Nitro Group in Organic Synthesis also emphasizes environmentally-friendly methods for nitration, the importance of aliphatic nitro compounds, and modern preparation of nitro compounds. Other topics discussed include: Henry reaction Asymmetric Michael addition Alkylation, acylation, halogenation, and related reactions of RNO2 Substitution and elimination of NO2 and RNO2 The Nitro Group in Organic Synthesis is a useful resource for researchers and students in organic and medicinal chemistry.
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Citations
Cited by
Organocatalytic Carbon–Sulfur Bond-Forming Reactions
Chauhan, P., Mahajan, S., & Enders, D. (2014) · Chemical Reviews · doi:10.1021/cr500235v · Cited by 632
Xuan, J., & Studer, A. (2017) · Chemical Society Reviews · doi:10.1039/c6cs00912c · Cited by 482
Umpolung reactivity in amide and peptide synthesis
Shen, B., Makley, D. M., & Johnston, J. N. (2010) · Nature · doi:10.1038/nature09125 · Cited by 318
Reversible Post-translational Modification of Proteins by Nitrated Fatty Acids in Vivo
Batthyany, C., Schopfer, F. J., Baker, P. R. S., Durán, R., Baker, L. M. S., Huang, Y., Cerveñansky, C., Branchaud, B. P., & Freeman, B. A. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m602814200 · Cited by 285
Duan, Y., Song, T., Dong, X., & Yang, Y. (2018) · Green Chemistry · doi:10.1039/c8gc00619a · Cited by 118
Metadata
- Authors
- Ono, N.
- Venue
- Wiley eBooks
- Publisher
- Wiley
- Published
- 2001-04-02
- OpenAlex
- W2487413726
- Cited by
- 1,616
- References
- 0
- FWCI
- 10.90
- Type
- book
- Language
- en
- Open access
- closed
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