Reductive amination of ferrocenylformylpyrazoles View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2010-02

AUTHORS

A. N. Rodionov, A. A. Simenel, Yu. S. Nekrasov, V. V. Kachal, E. Yu. Osipova, K. Ya. Zherebker

ABSTRACT

1-Aryl-3-ferrocenyl-4-formylpyrazoles were obtained from appropriate acetylferrocene arylhydrazones by the Vilsmeier—Haack reaction. Direct reductive amination of the resulting aldehydes with primary and secondary amines and amino acid esters in the presence of NaBH(OAc)3 was studied.

PAGES

405-410

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-010-0093-4

DOI

http://dx.doi.org/10.1007/s11172-010-0093-4

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1035706545


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