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Novel Selenium-Mediated Rearrangements and Cyclisations
In his thesis, Sohail Shahzad carefully investigates carbon nucleophiles in selenocyclisations, as well as reaction protocols for performing such reactions catalytically. After a comprehensive introduction to the element selenium, the author goes on to report the synthesis of several substrates for...
| Clasificación: | Libro Electrónico |
|---|---|
| Autor principal: | |
| Autor Corporativo: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Berlin, Heidelberg :
Springer Berlin Heidelberg : Imprint: Springer,
2013.
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| Edición: | 1st ed. 2013. |
| Colección: | Springer Theses, Recognizing Outstanding Ph.D. Research,
77 |
| Temas: | |
| Acceso en línea: | Texto Completo |
MARC
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| 001 | 978-3-642-33173-2 | ||
| 003 | DE-He213 | ||
| 005 | 20220117132607.0 | ||
| 007 | cr nn 008mamaa | ||
| 008 | 121026s2013 gw | s |||| 0|eng d | ||
| 020 | |a 9783642331732 |9 978-3-642-33173-2 | ||
| 024 | 7 | |a 10.1007/978-3-642-33173-2 |2 doi | |
| 050 | 4 | |a QD241-441 | |
| 072 | 7 | |a PNN |2 bicssc | |
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| 072 | 7 | |a PNN |2 thema | |
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| 100 | 1 | |a Shahzad, Sohail Anjum. |e author. |4 aut |4 http://id.loc.gov/vocabulary/relators/aut | |
| 245 | 1 | 0 | |a Novel Selenium-Mediated Rearrangements and Cyclisations |h [electronic resource] / |c by Sohail Anjum Shahzad. |
| 250 | |a 1st ed. 2013. | ||
| 264 | 1 | |a Berlin, Heidelberg : |b Springer Berlin Heidelberg : |b Imprint: Springer, |c 2013. | |
| 300 | |a XX, 192 p. |b online resource. | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
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| 347 | |a text file |b PDF |2 rda | ||
| 490 | 1 | |a Springer Theses, Recognizing Outstanding Ph.D. Research, |x 2190-5061 ; |v 77 | |
| 505 | 0 | |a General Introduction on Selenium.- The Synthesis of Novel Dihydronaphthalenes and Benzofluorenes -- The Synthesis of Naphthalenes and Biaryls -- Synthesis of Isocoumarins and Dihydroisocoumarins.- Experimental Section. | |
| 520 | |a In his thesis, Sohail Shahzad carefully investigates carbon nucleophiles in selenocyclisations, as well as reaction protocols for performing such reactions catalytically. After a comprehensive introduction to the element selenium, the author goes on to report the synthesis of several substrates for carbocyclisation reactions and the use of selenium reagents for the preparation of dihydronaphthalenes. Further chapters detail electrophilic selenium-mediated reactions, and novel strategies using selenium catalysts together with stoichiometric amounts of hypervalent iodine reagents as oxidants to convert stilbene carbosylic acids into the corresponding isocoumarins. This thesis outlines some excellent new synthetic routes which will be useful tools for synthetic organic chemistry in the future. | ||
| 650 | 0 | |a Chemistry, Organic. | |
| 650 | 0 | |a Inorganic chemistry. | |
| 650 | 0 | |a Chemistry. | |
| 650 | 1 | 4 | |a Organic Chemistry. |
| 650 | 2 | 4 | |a Inorganic Chemistry. |
| 650 | 2 | 4 | |a Chemistry. |
| 710 | 2 | |a SpringerLink (Online service) | |
| 773 | 0 | |t Springer Nature eBook | |
| 776 | 0 | 8 | |i Printed edition: |z 9783642331749 |
| 776 | 0 | 8 | |i Printed edition: |z 9783642428746 |
| 776 | 0 | 8 | |i Printed edition: |z 9783642331725 |
| 830 | 0 | |a Springer Theses, Recognizing Outstanding Ph.D. Research, |x 2190-5061 ; |v 77 | |
| 856 | 4 | 0 | |u https://doi.uam.elogim.com/10.1007/978-3-642-33173-2 |z Texto Completo |
| 912 | |a ZDB-2-CMS | ||
| 912 | |a ZDB-2-SXC | ||
| 950 | |a Chemistry and Materials Science (SpringerNature-11644) | ||
| 950 | |a Chemistry and Material Science (R0) (SpringerNature-43709) | ||