Reactions of selected 3-bromoisothiazole-5-carbonitriles with the secondary dialkylamines pyrrolidine and morpholine

doi:10.1016/J.TET.2014.06.012

Paper

Reactions of selected 3-bromoisothiazole-5-carbonitriles with the secondary dialkylamines pyrrolidine and morpholine

Published Oct 7, 2014 · A. Kalogirou, P. Koutentis

Tetrahedron

Q3 SJR score

8

Citations

0

Influential Citations

Full textSemantic Scholar

Abstract

Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.

Study Snapshot

3-bromoisothiazole-5-carbonitriles react with pyrrolidine or morpholine to produce 3-amino-substituted derivatives in high yields, with variations in reaction mechanisms and side products formation.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Reactions of selected 3-bromoisothiazole-5-carbonitriles with the secondary dialkylamines pyrrolidine and morpholine

References

Citations