Endogenous water-triggered and ultrasound accelerated synthesis of 1,5-disubstituted tetrazoles via a solvent and catalyst-free Ugi-azide reaction-Reference-Cited by-同舟云学术

Endogenous water-triggered and ultrasound accelerated synthesis of 1,5-disubstituted tetrazoles via a solvent and catalyst-free Ugi-azide reaction

Published:2017 Issue:5 Volume:19 Page:1259-1262
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Pharande Shrikant G.¹²³⁴⁵,Corrales Escobosa Alma Rosa¹²³⁴⁵,Gámez-Montaño Rocío¹²³⁴⁵^ORCID

Affiliation:

1. Departamento de Química

2. División de Ciencias Naturales y Exactas

3. Universidad de Guanajuato

4. Guanajuato

5. México

Abstract

An ultrasound accelerated, environmentally benign Ugi-azide based method was developed for the synthesis of 1,5-disubstituted tetrazoles under solvent and catalyst-free conditions.

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/GC/C6GC03324E

Reference32 articles.

1. Conformational mimicry. 1. 1,5-Disubstituted tetrazole ring as a surrogate for the cis amide bond

2. Medicinal chemistry of tetrazoles

3. Synthesis, Characterization, and Biological Activities of Pendant Arm‐Pyridyltetrazole Copper(II) Complexes: DNA Binding/Cleavage Activity and Cytotoxic Studies

4. Triazoles and tetrazoles: Prime ligands to generate remarkable coordination materials

5. A new tetrazole based turn-on fluorescence chemosensor for Zn2+ ions and its application in bioimaging

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