1996
DOI: 10.1007/bf01164870
|View full text |Cite
|
Sign up to set email alerts
|

Highly polarized enamines. 2. Synthesis and investigation of the further amination of derivatives of ?,?-DIAMINO-?-cyano-?-nitroethylene

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
6
0

Year Published

1998
1998
2015
2015

Publication Types

Select...
4
1

Relationship

1
4

Authors

Journals

citations
Cited by 5 publications
(6 citation statements)
references
References 2 publications
0
6
0
Order By: Relevance
“…The authors showed that this transformation is also valid for a considerable variety of 6-amino derivatives. On the other hand, attempts to prepare enediamines containing arylamino group in α-position of the enamine encountered considerable difficulties [65]. Deactivating influence of 6-arylamino group upon 4-chlorine atom is less pronounced than in the case of amino or alkylamino substituent and, hence, interaction between 4,6-dichloro-5-nitropyrimidine 96 and aromatic amines proceeds ambiguously, giving rise not only to the target chloropyrimidines, but also to 4,6-bisarylamino-5-nitropyrimidines 98, which cannot undergo transformation into enamines.…”
Section: Reactions Resulting In Formation Of Acyclic Enamine Derivatimentioning
confidence: 99%
“…The authors showed that this transformation is also valid for a considerable variety of 6-amino derivatives. On the other hand, attempts to prepare enediamines containing arylamino group in α-position of the enamine encountered considerable difficulties [65]. Deactivating influence of 6-arylamino group upon 4-chlorine atom is less pronounced than in the case of amino or alkylamino substituent and, hence, interaction between 4,6-dichloro-5-nitropyrimidine 96 and aromatic amines proceeds ambiguously, giving rise not only to the target chloropyrimidines, but also to 4,6-bisarylamino-5-nitropyrimidines 98, which cannot undergo transformation into enamines.…”
Section: Reactions Resulting In Formation Of Acyclic Enamine Derivatimentioning
confidence: 99%
“…It has been found recently 119 that the `push-pull' enamines 129 with at least one nonsubstituted amino group readily react with amidoacetals to give the corresponding amidines 130 and 131 and the reaction rate depends on the extent of of the other amino group (NH 2 > NHMe > NMe 2 ).…”
Section: Reactions Of B Bb B-disubstituted Ketene Nn-acetals With Ele...mentioning
confidence: 99%
“…Pyrido [2,3‐d]pyrimidines present particularly valuable biological activities such as antitumor , antimicrobial , diuretic , inhibiting dihydrofolate reductases, and tyrosine kinases . Enamines have been successfully utilized as building blocks for the synthesis of polyfunctionalized heterocycles and other related condensed system . In this repot a rapid one‐pot synthesis of enediamines with high yield and pure crystals by using arylazomalononitriles, whereas enediamines reported earlier after six separated successful steps .…”
Section: Introductionmentioning
confidence: 99%