Nucleophilic aromatic substitution reaction of some 3-nitroimidazo[1,2-a]pyridines with thioglycolate anion in DMF
β Scribed by Teulade, Jean Claude; Grassy, Gerard; Escale, Roger; Chapat, Jean Pierre
- Book ID
- 115458125
- Publisher
- American Chemical Society
- Year
- 1981
- Tongue
- English
- Weight
- 601 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-3263
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## Abstract magnified image In some nucleophilic substitution reactions of 2βcyanoβ3βnitroimidazo[1,2β__a__]pyridine, nitrogen (alkylamines, guanidine) and oxygen nucleophiles (alkoxides) underwent substitution of the 2βcyano group, while sulfur nucleophiles (alkylthiols) underwent substitution of
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Ever since Servis' first observed by NMR spectrometry that in DMSO much faster formation of 1,3\_disubstituted anionic o complex (hereinafter referred to as 1,3-adduct) from 2,4,6\_trinitroanisole (TNA) and 'OCH3 is followed by a much slower attack on the l-position, considerable attention has been