the Nitration of 2-Aminopyridines and 2-Aminothiazoles.

the Nitration of 2-Aminopyridines and 2-Aminothiazoles.

The mixed acid nitration ot 2-aminopyridines gives 2-nitramino pyridines in good yields. Since these nitramino pyridines can theoretically exist in two tautomeric forms, the possibility of isolating the alkyl derivatives of these forms was undertaken. Compounds such as 2-nitramino pyridine, 2-nitram...

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Main Author: Viron, Silvio J.
Other Authors: Taurins, A. (Supervisor)
Format: Others
Language:en
Published: McGill University 1952
Subjects:
Chemistry.
Online Access:http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=108640
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spelling ndltd-LACETR-oai-collectionscanada.gc.ca-QMM.1086402014-02-13T03:45:25Zthe Nitration of 2-Aminopyridines and 2-Aminothiazoles.Viron, Silvio J.Chemistry.The mixed acid nitration ot 2-aminopyridines gives 2-nitramino pyridines in good yields. Since these nitramino pyridines can theoretically exist in two tautomeric forms, the possibility of isolating the alkyl derivatives of these forms was undertaken. Compounds such as 2-nitramino pyridine, 2-nitramino-4-methyl pyridine and a new compound 2-nitramino-4, 6-dimethyl-3(5)-nitro pyridine were allowed to react with diazomethane, diazoethane and diazopropane and the products isolated.McGill UniversityTaurins, A. (Supervisor)1952.Electronic Thesis or Dissertationapplication/pdfenalephsysno: NNNNNNNNNTheses scanned by McGill Library.All items in eScholarship@McGill are protected by copyright with all rights reserved unless otherwise indicated.Doctor of Philosophy. (Department of Chemistry.) http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=108640
collection NDLTD
language en
format Others
sources NDLTD
topic Chemistry.
spellingShingle Chemistry.

Viron, Silvio J.
the Nitration of 2-Aminopyridines and 2-Aminothiazoles.
description The mixed acid nitration ot 2-aminopyridines gives 2-nitramino pyridines in good yields. Since these nitramino pyridines can theoretically exist in two tautomeric forms, the possibility of isolating the alkyl derivatives of these forms was undertaken. Compounds such as 2-nitramino pyridine, 2-nitramino-4-methyl pyridine and a new compound 2-nitramino-4, 6-dimethyl-3(5)-nitro pyridine were allowed to react with diazomethane, diazoethane and diazopropane and the products isolated.
author2 Taurins, A. (Supervisor)
author_facet Taurins, A. (Supervisor)
Viron, Silvio J.
author Viron, Silvio J.
author_sort Viron, Silvio J.
title the Nitration of 2-Aminopyridines and 2-Aminothiazoles.
title_short the Nitration of 2-Aminopyridines and 2-Aminothiazoles.
title_full the Nitration of 2-Aminopyridines and 2-Aminothiazoles.
title_fullStr the Nitration of 2-Aminopyridines and 2-Aminothiazoles.
title_full_unstemmed the Nitration of 2-Aminopyridines and 2-Aminothiazoles.
title_sort nitration of 2-aminopyridines and 2-aminothiazoles.
publisher McGill University
publishDate 1952
url http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=108640
work_keys_str_mv AT vironsilvioj thenitrationof2aminopyridinesand2aminothiazoles
AT vironsilvioj nitrationof2aminopyridinesand2aminothiazoles
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