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|a 9783319306322
|9 978-3-319-30632-2
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|a 10.1007/978-3-319-30632-2
|2 doi
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|a QD241-441
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|a 547
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|a Milestones in Microwave Chemistry
|h [electronic resource] /
|c edited by György Keglevich.
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|a 1st ed. 2016.
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|a Cham :
|b Springer International Publishing :
|b Imprint: Springer,
|c 2016.
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|a IX, 110 p. 144 illus., 4 illus. in color.
|b online resource.
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|a text
|b txt
|2 rdacontent
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|a computer
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|a online resource
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|a text file
|b PDF
|2 rda
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|a SpringerBriefs in Green Chemistry for Sustainability,
|x 2452-185X
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|a The Spread of the Application of the Microwave Technique in Organic Synthesis -- Microwave-Assisted Sytheses in Organic Chemistry -- The Use of MW in Organophosphorus Chemistry -- Interpretation of the Effects of Microwaves.
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|a This book looks back on thirty-five years of microwave (MW) chemistry and explains how the application of the MW technique became an integral part of R&D, eventually becoming recognized in industry. Further, it details how MW chemistry has undergone a dynamic development in the past three decades, one driven by the advent of increasingly sophisticated professional MW reactors in place of the kitchen MW ovens used in earlier years. A major part of the book shows how substitutions, esterifications, amidations, hydrolyses, alkylations, eliminations, dehydrations, condensations, cyclizations, C-C couplings and the modification of heterocycles can be performed advantageously under MW irradiation, as the reaction times are shorter, while the selectivity and yields are higher; it also explains why in most cases, the reactions can be performed under solvent-free conditions. MW irradiation within the sphere of organophosphorus chemistry is showcased and typical reactions, such as the direct derivatization of phosphinic acids, alkylating esterifications, Diels-Alder reactions, the inverse Wittig-type reaction, fragmentations, the Arbuzov reaction, the synthesis of α-hydroxyphosphonates and α-aminophosphonates (the Kabachnik-Fields condensation), deoxygenations and P-C coupling reactions are described under MW conditions. In closing, the advantages of MW chemistry such as faster reactions and the possibility of simplifying the catalytic systems are addressed.
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|a Chemistry, Organic.
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|a Chemistry, Technical.
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|a Science-History.
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|a Organic Chemistry.
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|a Industrial Chemistry.
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|a History of Science.
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|a Keglevich, György.
|e editor.
|4 edt
|4 http://id.loc.gov/vocabulary/relators/edt
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|a SpringerLink (Online service)
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|t Springer Nature eBook
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|i Printed edition:
|z 9783319306308
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|i Printed edition:
|z 9783319306315
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|a SpringerBriefs in Green Chemistry for Sustainability,
|x 2452-185X
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856 |
4 |
0 |
|u https://doi.uam.elogim.com/10.1007/978-3-319-30632-2
|z Texto Completo
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|a ZDB-2-CMS
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|a ZDB-2-SXC
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|a Chemistry and Materials Science (SpringerNature-11644)
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|a Chemistry and Material Science (R0) (SpringerNature-43709)
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