Tele nucleophilic aromatic substitutions in 1-nitro-3-and 1,3-dinitro-5-trichloromethylbenzene, and 3-trichloromethylbenzonitrile. A new synthesis of the 1,4-benzothiazine-3(4H)-one ring system from 3-nitrobenzoic acid

dc.contributor.authorGiannopoulos, T.en
dc.contributor.authorFerguson, J. R.en
dc.contributor.authorWakefield, B. J.en
dc.contributor.authorVarvounis, G.en
dc.date.accessioned2015-11-24T16:50:01Z
dc.date.available2015-11-24T16:50:01Z
dc.identifier.issn0040-4020-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9558
dc.rightsDefault Licence-
dc.subjectbenzenesen
dc.subjectreductionen
dc.subjectbenzothiazinesen
dc.subjectmechanismen
dc.titleTele nucleophilic aromatic substitutions in 1-nitro-3-and 1,3-dinitro-5-trichloromethylbenzene, and 3-trichloromethylbenzonitrile. A new synthesis of the 1,4-benzothiazine-3(4H)-one ring system from 3-nitrobenzoic aciden
heal.abstract3-Trichloromethylnitrobenzene 2, 1,3-dinitro-5-trichloromethylbenzene 13 and 3-trichloromethylbenzonitrile 18 react with sodium methoxide to give 4-methoxy-3-nitrobenzaldehyde 6, 4-methoxy-3,5-dinitrobenzaldehyde 15 and 5-dimethoxymethyl-2-methoxybenzonitrile 19, respectively. Compounds 2 and 13 react with methyl thioglycolate to afford dichloromethylacetates 7 and 16, respectively. These products are the result of tele nucleophilic aromatic substitution. Compound 18 reacted with methyl thioglycolate to give acetate 20 resulting from nucleophilic displacement of cyanide. Reductive cyclisation of 7 afforded benzothiazine 11. (C) 2000 Elsevier Science Ltd. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDoi 10.1016/S0040-4020(99)01012-1-
heal.identifier.secondary<Go to ISI>://000084896900014-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0040402099010121/1-s2.0-S0040402099010121-main.pdf?_tid=b822c4ea-34ac-11e3-a1cc-00000aacb361&acdnat=1381740398_e6089ce1cb523d049b67f129439a4468-
heal.journalNameTetrahedronen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2000-
heal.publisherElsevieren
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

Αρχεία

Φάκελος/Πακέτο αδειών

Προβολή: 1 - 1 of 1
Φόρτωση...
Μικρογραφία εικόνας
Ονομα:
license.txt
Μέγεθος:
1.74 KB
Μορφότυπο:
Item-specific license agreed upon to submission
Περιγραφή: