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| Fältnamn | Indikatorer | Metadata |
|---|---|---|
| 000 | 02448naa a2200385 4500 | |
| 001 | oai:gup.ub.gu.se/170412 | |
| 003 | SwePub | |
| 008 | 240528s2012 | |||||||||||000 ||eng| | |
| 009 | oai:research.chalmers.se:c0b46683-2d13-462b-b4e2-4289c78ed8c3 | |
| 024 | 7 | a https://gup.ub.gu.se/publication/1704122 URI |
| 024 | 7 | a https://doi.org/10.1021/ol303036j2 DOI |
| 024 | 7 | a https://research.chalmers.se/publication/1704122 URI |
| 040 | a (SwePub)gud (SwePub)cth | |
| 041 | a eng | |
| 042 | 9 SwePub | |
| 072 | 7 | a ref2 swepub-contenttype |
| 072 | 7 | a art2 swepub-publicationtype |
| 100 | 1 | a Ekebergh, Andreas,d 1984u Chalmers tekniska högskola,Chalmers University of Technology4 aut0 (Swepub:cth)ekebergh |
| 245 | 1 0 | a Total Synthesis of Nostodione A, a Cyanobacterial Metabolite |
| 264 | c 2012-12-10 | |
| 264 | 1 | b American Chemical Society (ACS),c 2012 |
| 338 | a electronic2 rdacarrier | |
| 520 | a The first total synthesis of the mitotic spindle poison nostodione A is described. The inherent oxidative sensitivity of indoles is utilized for a late introduction of a second carbonyl to the cyclopent[b]indole-2-one system. The tricyclic system is prepared from indole-3-acetic acid and O-silylated 4-ethynylphenol, using a stereoselective intramolecular reductive Heck cyclization as the key transformation. | |
| 650 | 7 | a NATURVETENSKAPx Kemi0 (SwePub)1042 hsv//swe |
| 650 | 7 | a NATURAL SCIENCESx Chemical Sciences0 (SwePub)1042 hsv//eng |
| 700 | 1 | a Börje, Anna,d 1961u Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology,University of Gothenburg4 aut0 (Swepub:gu)xboann |
| 700 | 1 | a Mårtensson, Jerker,d 1965u Chalmers tekniska högskola,Chalmers University of Technology4 aut0 (Swepub:cth)jerker |
| 710 | 2 | a Chalmers tekniska högskolab Institutionen för kemi och molekylärbiologi4 org |
| 773 | 0 | t Organic Lettersd : American Chemical Society (ACS)g 14:24, s. 6274-6277q 14:24<6274-6277x 1523-7060x 1523-7052 |
| 856 | 4 | u https://gup.ub.gu.se/publication/170412x primaryx freey FULLTEXT |
| 856 | 4 | u https://doi.org/10.1021/ol303036j |
| 856 | 4 | u http://publications.lib.chalmers.se/records/fulltext/170412/local_170412.pdfx primaryx freey FULLTEXT |
| 856 | 4 8 | u https://gup.ub.gu.se/publication/170412 |
| 856 | 4 8 | u https://doi.org/10.1021/ol303036j |
| 856 | 4 8 | u https://research.chalmers.se/publication/170412 |
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