In:
European Journal of Organic Chemistry, Wiley, Vol. 2017, No. 47 ( 2017-12-22), p. 7148-7159
Abstract:
A series of new heteroannulated pyrido[2,3‐ c ]coumarins have been prepared by the domino reactions of chromone‐3‐carboxylic acid derivatives with electron‐rich binucleophilic aminoheterocycles. The products contain the core structures of coumarin, pyridine, and an annulated five‐membered heterocyclic system, namely pyrazole, pyrrole, or isoazole. The fluorescence of the products was investigated. The products inhibit ecto‐5′‐nucleotidase (e5′NT) enzymatic activity.
Type of Medium:
Online Resource
ISSN:
1434-193X
,
1099-0690
DOI:
10.1002/ejoc.v2017.47
DOI:
10.1002/ejoc.201701276
Language:
English
Publisher:
Wiley
Publication Date:
2017
detail.hit.zdb_id:
1475010-7
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