Microwave-assisted regioselective [1,3]-dipolar cycloaddition of 3-methyl-2-(substitutedbenzylidene)-5-oxopyrazolidin-2-ium-1-ides to benzothiophene 1,1-dioxide

Authors

YAŞAR DÜRÜST
EDA SAĞIRLI
AKIN SAĞIRLI

DOI

10.3906/kim-1502-3

Abstract

A series of pyrazolidinium ylides was reacted with benzothiophene 1,1-dioxide to afford (3R,5S,5aS,10bS)-3-methyl-5-substitutedphenyl-2,3,5,5a-tetrahydrobenzo[4,5]thieno[3,2-c]pyrazolo[1,2-a]pyrazol-1(10bH)-one 6,6-dioxides under microwave irradiation and their structures were identified by means of spectral/physical characteristics including X-ray diffraction data and HRMS measurements.

Keywords

Microwave-assisted synthesis, pyrazolidinium, ylide, 1, 3-dipolar cycloaddition, benzothiophene dioxide

First Page

789

Last Page

800

Recommended Citation

DÜRÜST, YAŞAR; SAĞIRLI, EDA; and SAĞIRLI, AKIN (2015) "Microwave-assisted regioselective [1,3]-dipolar cycloaddition of 3-methyl-2-(substitutedbenzylidene)-5-oxopyrazolidin-2-ium-1-ides to benzothiophene 1,1-dioxide," Turkish Journal of Chemistry: Vol. 39: No. 4, Article 7. https://doi.org/10.3906/kim-1502-3
Available at: https://journals.tubitak.gov.tr/chem/vol39/iss4/7