Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.11889/3995| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | El-Sayrafi, Sami | |
| dc.contributor.author | Rayyan, Saleh | |
| dc.date.accessioned | 2017-01-03T08:29:10Z | |
| dc.date.available | 2017-01-03T08:29:10Z | |
| dc.date.issued | 2001 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.11889/3995 | |
| dc.description.abstract | Both pyrophosphoryl chloride and phosphorus oxychloride react with aryl-aliphatic acids to form mixed anhydrides which undergo intramolecular acylation to afford cyclic ketones without the addition of a Friedel-Crafts catalyst. Aryl and aroyl-benzoic acids could be cyclized to the corresponding anthrones and anthraquinones respectively. | en_US |
| dc.language.iso | en | en_US |
| dc.subject | Acylation | en_US |
| dc.subject | Aliphatic compounds - Synthesis | en_US |
| dc.subject | Ketones - Synthesis | en_US |
| dc.subject | Anthraquinones - Spectra | en_US |
| dc.title | Intramolecular Acylation of Aryl- and Aroyl-Aliphatic Acids by the Action of Pyrophosphoryl Chloride and Phosphorus Oxychloride | en_US |
| dc.type | Article | en_US |
| newfileds.department | Science | en_US |
| newfileds.item-access-type | open_access | en_US |
| newfileds.thesis-prog | none | en_US |
| newfileds.general-subject | Natural Sciences | العلوم الطبيعية | en_US |
| item.fulltext | With Fulltext | - |
| item.grantfulltext | open | - |
| item.languageiso639-1 | other | - |
| Appears in Collections: | Fulltext Publications | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Intramolecular Acylation of Aryl- and Aroyl-Ali.pdf | 29.79 kB | Adobe PDF | View/Open |
Page view(s)
98
Last Week
1
1
Last month
5
5
checked on Apr 14, 2024
Download(s)
23
checked on Apr 14, 2024
Google ScholarTM
Check
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.