Budzikiewicz, Herbert (2016). The ortho-quinol acetates (die ortho-Chinolacetate): 20 years of dedicated research in Vienna and what happened then? Mon. Chem., 147 (4). S. 627 - 664. WIEN: SPRINGER WIEN. ISSN 1434-4475
Full text not available from this repository.Abstract
o-Quinol acetates (o-Chinolacetate) were the main research field of the Organic Chemistry Institute in Vienna (Austria) for two decades beginning in 1950. The possibility to react them with various kinds of compounds was exploited for the synthesis of structural types not easily accessible on other ways. They became the basis for investigations, e.g. in photochemistry, in reaction mechanistic studies of various rearrangement reactions, or the Diels-Alder reaction. Even in the natural products chemistry o-quinol structures can be found comprising Diels-Alder dimeric terpenes. Most of the original publications had appeared in Monatshefte fur Chemie written in German. This might explain a statement from the year 2000 that These findings add to our knowledge of the largely unexplored chemistry of o-quinolsaEuro broken vertical bar. (Nicolaou et al. in J Am Chem Soc 122:3071, 2000). This review is intended to wake up slumbering knowledge.
| Item Type: | Journal Article | ||||||||
| Creators: |
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| URN: | urn:nbn:de:hbz:38-280272 | ||||||||
| DOI: | 10.1007/s00706-015-1635-0 | ||||||||
| Journal or Publication Title: | Mon. Chem. | ||||||||
| Volume: | 147 | ||||||||
| Number: | 4 | ||||||||
| Page Range: | S. 627 - 664 | ||||||||
| Date: | 2016 | ||||||||
| Publisher: | SPRINGER WIEN | ||||||||
| Place of Publication: | WIEN | ||||||||
| ISSN: | 1434-4475 | ||||||||
| Language: | English | ||||||||
| Faculty: | Unspecified | ||||||||
| Divisions: | Unspecified | ||||||||
| Subjects: | no entry | ||||||||
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| Refereed: | Yes | ||||||||
| URI: | http://kups.ub.uni-koeln.de/id/eprint/28027 |
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