| 000 | 02867nam a22004695i 4500 | ||
|---|---|---|---|
| 001 | 978-3-319-00702-1 | ||
| 003 | DE-He213 | ||
| 005 | 20140220082839.0 | ||
| 007 | cr nn 008mamaa | ||
| 008 | 130809s2013 gw | s |||| 0|eng d | ||
| 020 |
_a9783319007021 _9978-3-319-00702-1 |
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| 024 | 7 |
_a10.1007/978-3-319-00702-1 _2doi |
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| 050 | 4 | _aQD410-412.5 | |
| 072 | 7 |
_aPNND _2bicssc |
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| 072 | 7 |
_aSCI013040 _2bisacsh |
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| 082 | 0 | 4 |
_a547.05 _223 |
| 100 | 1 |
_aEscribano Cuesta, Ana. _eauthor. |
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| 245 | 1 | 0 |
_aNew Gold-Catalyzed Reactions and Applications for the Synthesis of Alkaloids _h[electronic resource] / _cby Ana Escribano Cuesta. |
| 264 | 1 |
_aCham : _bSpringer International Publishing : _bImprint: Springer, _c2013. |
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| 300 |
_aXIII, 195 p. 280 illus., 41 illus. in color. _bonline resource. |
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| 336 |
_atext _btxt _2rdacontent |
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| 337 |
_acomputer _bc _2rdamedia |
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| 338 |
_aonline resource _bcr _2rdacarrier |
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| 347 |
_atext file _bPDF _2rda |
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| 490 | 1 |
_aSpringer Theses, Recognizing Outstanding Ph.D. Research, _x2190-5053 |
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| 505 | 0 | _aIntroduction -- General Objectives -- Gold(I)-Catalyzed Reactions of 1,6-Enynes with Aldehydes: Cycloaddition versus Metathesis-Type Reactions -- Formation of Cyclobutene Compounds via Gold(I)-Catalyzed Cycloisomerization of 1,n-Enynes -- Approach Toward the Total Synthesis of Lundurines. | |
| 520 | _aAna Escribano Cuesta's thesis presents a detailed study of the inter- and intramolecular reactions of carbonyl compounds with 1,6-enynes using gold (I) complexes. An important part of the work involved streamlining the variables that allow the selective synthesis of different products such as tricyclic compounds, dihydropyrans, 1,3-dienes or cyclobutenes. The second chapter highlights the importance and difficulties in synthesising a cyclobutene subunit and the author includes a detailed description of how the products were prepared. The final chapter outlines the synthesis of lundurines using methodology developed by the author's research group for intramolecular gold-catalyzed cyclization of indoles with alkynes. The lundurine products developed in this work show significant in vitro cytoxicity toward B16 melanoma cells. The work in this thesis has led to a number of publications in high-profile chemistry journals. | ||
| 650 | 0 | _aChemistry. | |
| 650 | 0 | _aChemistry, Organic. | |
| 650 | 0 | _aCatalysis. | |
| 650 | 1 | 4 | _aChemistry. |
| 650 | 2 | 4 | _aOrganometallic Chemistry. |
| 650 | 2 | 4 | _aCatalysis. |
| 650 | 2 | 4 | _aOrganic Chemistry. |
| 710 | 2 | _aSpringerLink (Online service) | |
| 773 | 0 | _tSpringer eBooks | |
| 776 | 0 | 8 |
_iPrinted edition: _z9783319007014 |
| 830 | 0 |
_aSpringer Theses, Recognizing Outstanding Ph.D. Research, _x2190-5053 |
|
| 856 | 4 | 0 | _uhttp://dx.doi.org/10.1007/978-3-319-00702-1 |
| 912 | _aZDB-2-CMS | ||
| 999 |
_c96466 _d96466 |
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