<i>N</i>-Propargylation of Indolo-Triterpenoids and Their Application in Mannich Reaction

Molbank. 2019;2019(2):M1065 DOI 10.3390/M1065

 

Journal Homepage

Journal Title: Molbank

ISSN: 1422-8599 (Print)

Publisher: MDPI AG

LCC Subject Category: Science: Chemistry: Inorganic chemistry

Country of publisher: Switzerland

Language of fulltext: English

Full-text formats available: PDF, HTML

 

AUTHORS

Elmira F. Khusnutdinova (Ufa Institute of Chemistry UFRS RAS, Ufa 450054, 71 pr. Oktyabrya, Russia)
Anastasiya V. Petrova (Ufa Institute of Chemistry UFRS RAS, Ufa 450054, 71 pr. Oktyabrya, Russia)
Gulnaz M. Bashirova (Chemical Department, Bashkir State University, Ufa 450076, 32 Validy Str., Russia)
Oxana B. Kazakova (Ufa Institute of Chemistry UFRS RAS, Ufa 450054, 71 pr. Oktyabrya, Russia)

EDITORIAL INFORMATION

Blind peer review

Editorial Board

Instructions for authors

Time From Submission to Publication: 11 weeks

 

Abstract | Full Text

The introduction of the alkynyl moiety to the triterpenic core through a linkage to the indole nitrogen is described. The reaction of <i>N</i>-propargylindoles with <i>N</i>-methylpiperazine using Mannich reaction led to propargylaminoalkynyl-triterpenoids, whose structures were established by NMR spectroscopy.