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Organotrifluoroborate Preparation, Coupling and Hydrolysis [electronic resource] / by Alastair J. J. Lennox.

By: Lennox, Alastair J. J [author.].
Contributor(s): SpringerLink (Online service).
Material type: TextTextSeries: Springer Theses, Recognizing Outstanding Ph.D. Research: Publisher: Cham : Springer International Publishing : Imprint: Springer, 2013Description: XV, 223 p. 308 illus., 96 illus. in color. online resource.Content type: text Media type: computer Carrier type: online resourceISBN: 9783319011349.Subject(s): Chemistry | Organic chemistry | Chemical engineering | Catalysis | Chemistry | Organic Chemistry | Catalysis | Industrial Chemistry/Chemical EngineeringAdditional physical formats: Printed edition:: No titleDDC classification: 547 Online resources: Texto completo
Contents:
General Introduction -- Organotrifluoroborate Preparation -- Organotrifluoroborate Coupling -- Organotrifluoroborate Hydrolysis -- Conclusions and Future Work -- Experimental: General Experimental Details -- Experimental: Organotrifluoroborate Preparation -- Experimental: Organotrifluoroborate Coupling -- Experimental: Organotrifluoroborate Hydrolysis.
In: Springer eBooksSummary: Alistair Lennox's thesis reports on the reactivity of organotrifluoroborates, which are becoming increasingly important reagents in synthesis. The thesis is divided into three sections. The first section describes a method for preparing organotrifluoroborates. The second section reports on a mechanistic investigation into the main application of RBF3K reagents as coupling partners in Suzuki-Miyaura coupling, phenomena identified as arising from organotrifluoroborate hydrolysis and fluoride release. The final section reports on a detailed investigation into the hydrolysis mechanism, a prerequisite for their Suzuki-Miyaura coupling, and how it may be predicted and controlled. This research has uncovered many interesting and useful details and shows how problems associated with Suzuki-Miyaura coupling can best be addressed. There has already been wide industrial uptake of the new procedures and insights. The broad nature and clear and succinct style will make the thesis a valuable resource for anyone working in synthesis, organometallic chemistry, or in homogeneous catalysis.
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Item type Current location Shelving location Call number Status Date due Barcode Item holds
Springer (Colección 2013) Springer (Colección 2013) BIBLIOTECA GENERAL
Química y Ciencias de Materiales Química y Ciencias de Materiales (Browse shelf) Available
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General Introduction -- Organotrifluoroborate Preparation -- Organotrifluoroborate Coupling -- Organotrifluoroborate Hydrolysis -- Conclusions and Future Work -- Experimental: General Experimental Details -- Experimental: Organotrifluoroborate Preparation -- Experimental: Organotrifluoroborate Coupling -- Experimental: Organotrifluoroborate Hydrolysis.

Alistair Lennox's thesis reports on the reactivity of organotrifluoroborates, which are becoming increasingly important reagents in synthesis. The thesis is divided into three sections. The first section describes a method for preparing organotrifluoroborates. The second section reports on a mechanistic investigation into the main application of RBF3K reagents as coupling partners in Suzuki-Miyaura coupling, phenomena identified as arising from organotrifluoroborate hydrolysis and fluoride release. The final section reports on a detailed investigation into the hydrolysis mechanism, a prerequisite for their Suzuki-Miyaura coupling, and how it may be predicted and controlled. This research has uncovered many interesting and useful details and shows how problems associated with Suzuki-Miyaura coupling can best be addressed. There has already been wide industrial uptake of the new procedures and insights. The broad nature and clear and succinct style will make the thesis a valuable resource for anyone working in synthesis, organometallic chemistry, or in homogeneous catalysis.

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