Synthesis of Several 5α-Androstano[17,16-d]Pyrazolines from Tigogenin View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2014-12

AUTHORS

N. Sh. Nadaraia, M. L. Kakhabrishvili, E. O. Onashvili, N. N. Barbakadze, M. Z. Getia, A. Pichette, M. I. Sikharulidze, U. S. Makhmudov

ABSTRACT

New androstanopyrazolines and hydrazones were synthesized via acid-catalyzed condensation of the tigogenin transformation product 5α-pregnenolone with several hydrazines. Their structures were proved using IR and NMR spectroscopy and mass spectrometry. An x-ray crystal structure analysis was performed for pregnenolone p-nitrophenylhydrazone acetate.

PAGES

1024-1028

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10600-014-1151-1

DOI

http://dx.doi.org/10.1007/s10600-014-1151-1

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1052229108


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