maria del gamez

Prof. maria del gamez

Universidad de Guanajuato, Campus Guanajuato, División de Ciencias Naturales y Exactas, Departamento de Ingeniería Química
orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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29 May 2013 in Angewandte Chemie International Edition
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Journal Article
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MUMurali Venkata Basavanag Unnamatla
Murali Venkata Basavanag Unnamatla
ASAurélie Dos Santos
Aurélie Dos Santos
LKLaurent El Kaim
Laurent El Kaim
MGmaria del gamez
maria del gamez
LGLaurence Grimaud
Laurence Grimaud

1 February 2014 in Bioorganic & Medicinal Chemistry
Verified
Journal Article
Closed access
Pedro A. CanoPedro A. Cano
Pedro A. Cano
AIAlejandro Islas-Jácome
Alejandro Islas-Jácome
JMJOAQUIN GONZÁLEZ MARRERO
JOAQUIN GONZÁLEZ MARRERO
LYLilian Yépez-Mulia
Lilian Yépez-Mulia
FCFernando Calzada
Fernando Calzada
MGmaria del gamez
maria del gamez


17 January 2017 in Green Chemistry
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Journal Article
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SPShrikant G. Pharande
Shrikant G. Pharande
AEAlma Rosa Corrales Escobosa
Alma Rosa Corrales Escobosa
MGmaria del gamez
maria del gamez
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.

14 May 2018 in ACS Omega
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Journal Article
Open access
MCMiguel Ángel Claudio-Catalán
Miguel Ángel Claudio-Catalán
SPShrikant G. Pharande
Shrikant G. Pharande
AQAndrea Quezada-Soto
Andrea Quezada-Soto
KKKranthi G. Kishore
Kranthi G. Kishore
ARAngel Rentería-Gómez
Angel Rentería-Gómez
MGmaria del gamez
maria del gamez
A new, efficient, green, endogenous water-triggered, solvent- and catalyst-free ultrasound-assisted one-pot Groebke–Blackburn–Bienaymé reaction/SNAr/ring-chain azido-tautomerization strategy to synthesize bound-type fused bis-heterocycles imidazo or benzo[d]imidazo[2,1-b]thiazoles and 1,5-disubstituted tetrazole (1,5-DsT) containing quinoline moiety is described, which allows synthesis of two types of fused heterocycles in one step under mild green conditions. Antibacterial and antiamebic activities of selected newly synthesized compounds were carried out against three bacterial species: Gram-positive bacterium Staphylococcus aureus ATCC 6538 and Gram-negative bacteria Pseudomonas aeruginosa ATCC 13384 and Escherichia coli O55 and against one amebic species: Entamoeba histolytica.

31 July 2013 in Organic & Biomolecular Chemistry
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Journal Article
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RGRaul E. Gordillo-Cruz
Raul E. Gordillo-Cruz
ARAngel Rentería-Gómez
Angel Rentería-Gómez
AIAlejandro Islas-Jácome
Alejandro Islas-Jácome
CCCarlos J. Cortés-García
Carlos J. Cortés-García
Erik Díaz-CervantesErik Díaz-Cervantes
Erik Díaz-Cervantes
MGmaria del gamez
maria del gamez
A series of nine novel 3-tetrazolylmethyl-azepino[4,5-b]indol-4-ones were prepared in moderate to good overall yields in only two reaction steps. The first step consisted of a one-pot sequential process of an Ugi-azide multicomponent reaction, N-acylation and SN2 to give the xanthates. The second step was an intramolecular cyclization under free radical conditions. Also, their binding modes have been modelled using docking techniques.