EventsThe 21st International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session A. General Organic Synthesis of the event The 21st International Electronic Conference on Synthetic Organic Chemistry
Published date
03 Nov, 2017
Citation
Angel Rentería-Gómez, M. V. Basavanag Unnamatla, Rocío Gámez-Montaño, Bhavna Kaveti, Synthesis of bis-heterocycles type spacer containing 1,5-disubstituted-1H-tetrazoles, in Proceedings of The 21st International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2017, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-21-04776
Share
Email
Facebook
Twitter
LinkedIn

Synthesis of bis-heterocycles type spacer containing 1,5-disubstituted-1H-tetrazoles

Bhavna Kaveti 1
1. Universidad de Guanajuato
Abstract

1,5-Disustituted tetrazoles (1,5-DS-T) are useful heterocyclic moieties present in many bioactive compounds and drugs. Moreover, they are used as bidentate ligands in coordination chemistry, metal-organic framework science, bioimaging, photo-imaging, explosives, propellants, and high energy materials. In this work we report a series of ten new bis-heterocycles type spacer containing 1,5-disubstituted-1H-tetrazoles and furan, synthesized via Ugi-azide (UA) MCR in good to excellent yields (79-99%), using furfuryl amine as constant component and varying the aldehyde and isocyanide components in mild conditions. Additionally, the furan ring present in this bis-heterocycle has great importance in Diels-Alder cycloaddition reaction. As per our knowledge, there are no any previous reported methods available toward bis-heterocycles type spacer via UA.

Keywords
bis-heterocycles
1,5-disustituted tetrazole
Ugi-azide
Manuscript
Poster
ECSOC 2017 pdf.pdf
Rotation of a double C=N bond driven by palladium
STUDY OF KINETICS OF A THERMOSTABLE MATERIAL WITH GOLD NANOPARTICLES REINFORCED WITH NANOCLAY