Diazo reductive: a new approach to the synthesis of novel “upper rim” functionalized resorcin[4]arene Schiff-bases View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2008-10

AUTHORS

Vinod K. Jain, Parin H. Kanaiya

ABSTRACT

The tetraaminoresorcin[4]arene was synthesized, which otherwise could not be easily synthesized by conventional method, by first introducing the azo group at the upper rim, followed by its reduction with Na2S2O4. Tetraaminoresorcin[4]arene was then condensed with different aromatic aldehydes in ethanol at reflux temperature to obtain nine novel “upper rim” functionalized resorcin[4]arene Schiff-bases. All the nine Schiff-bases were characterized by m.p., elemental analysis, FT-IR, NMR and Mass spectral data. More... »

PAGES

111-115

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10847-008-9445-1

DOI

http://dx.doi.org/10.1007/s10847-008-9445-1

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1001916980


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