Events The 23rd International Electronic Conference on Synthetic Organic Chemistry

Event submissions

Published

This submission belongs to the session C. Microwave Assisted Synthesis of the event The 23rd International Electronic Conference on Synthetic Organic Chemistry

Published date

15 Nov, 2019

Citation

Sandra Cecilia Ramírez López, María del Rocio Gámez Montaño, Microwave assisted synthesis of bis-heterocycles containing the imidazo[1,2-a]pyridine by Groebke-Blackburn- Bienaymé reaction., in Proceedings of The 23rd International Electronic Conference on Synthetic Organic Chemistry, 15 November–15 December 2019, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-23-06648

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Microwave assisted synthesis of bis-heterocycles containing the imidazo[1,2-a]pyridine by Groebke-Blackburn- Bienaymé reaction.

María del Rocio Gámez Montaño ¹

Sandra Cecilia Ramírez López ¹

1. Universidad de Guanajuato, División de Ciencias Naturales y Exactas, Departamento de Química

Abstract

A serie of six fused bis-heterocycles having imidazo[1,2-a]pyridine frameworks bound with quinoline were synthesized by catalysis and solvent free, microwave assisted Groebke-Blackburn-Bienaymé reaction (GBBR). The synthesis of these compounds is of great interest in synthetic and medicinal chemistry because these heterocycles are considered privileged scaffolds.

Keywords

imidazo[1,2-a]pyridine

Groebke-Blackburn-Bienaymé reaction (GBBR)

2-Chloro-3-formyl-quinoline

Manuscript

sciforum-028344-ECSOC-GBB.pdf

Asymmetric Biginelli-like reaction catalyzed by chiral TADDOL-derived phosphoric acid bearing two hydroxyl groups

BIOACTIVE SESQUITERPENE OBTAINED FROM Schinus areira L. (Anacardiaceae) ESSENTIAL OIL