http://www.cnr.it/ontology/cnr/individuo/prodotto/ID216377
Condensation of Primary Nitro Compounds to Isoxazole Derivatives: Stoichiometric to Catalytic (Contributo in volume (capitolo o saggio))
- Type
- Label
- Condensation of Primary Nitro Compounds to Isoxazole Derivatives: Stoichiometric to Catalytic (Contributo in volume (capitolo o saggio)) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Alternative label
De Sarlo, Francesco; Machetti, Fabrizio (2014)
Condensation of Primary Nitro Compounds to Isoxazole Derivatives: Stoichiometric to Catalytic
Wiley-VCH Verlag Gmbh, Weinheim (Germania) in Methods and Applications of Cycloaddition Reactions in Organic Syntheses, 2014
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- De Sarlo, Francesco; Machetti, Fabrizio (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://www.wiley.com/WileyCDA/WileyTitle/productCd-1118299884.html (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#titoloVolume
- Methods and Applications of Cycloaddition Reactions in Organic Syntheses (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Istituto di Chimica dei Composti Organometallici del CNR, via Madonna del piano 10, 59100 Sesto Fiorentino, Firenze
Dipartimento di Chimica 'Ugo Schiff' dell'Università di Firenze, via Della Lastruccia 13, 59100 Sesto Fiorentino, Firenze (literal)
- Titolo
- Condensation of Primary Nitro Compounds to Isoxazole Derivatives: Stoichiometric to Catalytic (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#isbn
- 978-1-118-29988-3 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#curatoriVolume
- Nagatoshi Nishiwaki (literal)
- Abstract
- Advanced tools for developing new functional materials and applications in chemical research, pharmaceuticals, and materials science
Cycloadditions are among the most useful tools for organic chemists, enabling them to build carbocyclic and heterocyclic structures. These structures can then be used to develop a broad range of functional materials, including pharmaceuticals, agrochemicals, dyes, and optics. With contributions from an international team of leading experts and pioneers in cycloaddition chemistry, this book brings together and reviews recent advances, trends, and emerging research in the field.
Methods and Applications of Cycloaddition Reactions in Organic Syntheses focuses on two component cycloadditions, with chapters covering such topics as:
N1 unit transfer reaction to C-C double bonds
[3+2] Cycloaddition of ?, ?-unsaturated metal-carbene complexes
Formal [3+3] cycloaddition approach to natural product synthesis
Development of new methods for the construction of heterocycles based on cycloaddition reaction of 1,3-dipoles
Cycloreversion approach for preparation of large ?-conjugated compounds
Transition metal-catalyzed or mediated [5+1] cycloadditions
Readers will learn methods for seamlessly executing important reactions such as Diels-Alder and stereoselective dipolar reactions in order to fabricate heterocyclic compounds, natural products, and functional molecules. The book not only features cutting-edge topics, but also important background information, such as the contributors' process for developing new methodologies, to help novices become fully adept in the field. References at the end of each chapter lead to original research papers and reviews for facilitating further investigation of individual topics.
Covering the state of the science and technology, Methods and Applications of Cycloaddition Reactions in Organic Syntheses enables synthetic organic chemists to advance their research and develop new functional materials and applications in chemical research, pharmaceuticals, and materials science. (literal)
- Editore
- Prodotto di
- Autore CNR
Incoming links:
- Prodotto
- Autore CNR di
- Editore di