Access to the noryohimban [6,5,6,5,6] ring system via an intramolecular furan Diels-Alder reaction
| dc.contributor.author | Fokas, D. | en |
| dc.contributor.author | Patterson, J. E. | en |
| dc.contributor.author | Slobodkin, G. | en |
| dc.contributor.author | Baldino, C. M. | en |
| dc.date.accessioned | 2015-11-24T17:38:26Z | |
| dc.date.available | 2015-11-24T17:38:26Z | |
| dc.identifier.issn | 0040-4039 | - |
| dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/14491 | |
| dc.rights | Default Licence | - |
| dc.subject | substitution | en |
| dc.subject | chemistry | en |
| dc.title | Access to the noryohimban [6,5,6,5,6] ring system via an intramolecular furan Diels-Alder reaction | en |
| heal.abstract | Polycyclic indolic compounds containing the [6,5,6,5,6] ring system were prepared via an intramolecular furan Diels-Alder reaction of alpha,beta-unsaturated amides generated by the N-acylation of 1-(2-furyl)-beta-tetrahydrocarbolines. This chemistry can provide access to D(14)-noryohimban derivatives by exploiting the functionality on the C,DIE ring system of the corresponding cycloadducts. (C) 2003 Elsevier Science Ltd. All rights reserved. | en |
| heal.access | campus | - |
| heal.fullTextAvailability | TRUE | - |
| heal.identifier.primary | Doi 10.1016/S0040-4039(03)01179-1 | - |
| heal.identifier.secondary | <Go to ISI>://000183683500045 | - |
| heal.journalName | Tetrahedron Lett | en |
| heal.journalType | peer reviewed | - |
| heal.language | en | - |
| heal.publicationDate | 2003 | - |
| heal.publisher | Pergamon - Elsevier | en |
| heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Μηχανικών Επιστήμης Υλικών | el |
| heal.type | journalArticle | - |
| heal.type.el | Άρθρο Περιοδικού | el |
| heal.type.en | Journal article | en |
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