Aydeé Fuentes

Universidad Autónoma del Estado de México

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Moisés Romero‐Ortega

Universidad Autónoma del Estado de México

Carlos González

Instituto de Química Física Blas Cabrera

Erick Cuevas‐Yáñez

Universidad Autónoma del Estado de México

David Corona‐Becerril

Universidad Autónoma del Estado de México

Raymundo Cruz

Center for Research and Advanced Studies of the National Polytechnic Institute

Jaime González

Universidad Autónoma del Estado de México

Hugo A. Jiménez‐Vázquez

Instituto Politécnico Nacional

A. Guzmán

Hospital Infantil de México Federico Gómez

Rafael Martínez‐Palou

Mexican Institute of Petroleum

Joaquı́n Tamariz

Instituto Politécnico Nacional

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Universidad Autónoma del Estado de México

Universidad Nacional Autónoma de México

Instituto Politécnico Nacional

Rede de Química e Tecnologia

Tecnológico Nacional de México

Universidad de Cuautitlán Izcalli

Universidad Autónoma Metropolitana

Center for Research and Advanced Studies of the National Polytechnic Institute

Tribunal Electoral del Estado de México

Universidad de Guanajuato

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Desulfurization–Oxygenation of Chiral 1,3-Thiazolidine-2-thiones and 1,3-Oxazolidine-2-thiones Using Propylene Oxide and Microwave Irradiation

Synlett (2012)

Moisés Romero‐Ortega Leticia Minor‐Villar Rodolfo Tello‐Aburto Horacio F. Olivo Aydeé Fuentes

An efficient method for the desulfurization–oxygenation of 1,3-thiazolidine-2-thiones and 1,3-oxazolidine-2-thiones using propylene oxide and employing microwave irradiation is described. This strategy of oxygenation of the thiocarbonyl group provides an attractive methodology to prepare chiral 1,3-thiazolidin-2-ones and 1,3-oxazolidin-2-ones from the corresponding precursors in good yields.

Thiazolidine

Oxazolidine

Propylene oxide

10.1055/s-0032-1317525

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Citations (5)

The Use of Glucose as Alternative Reducing Agent in Copper-Catalyzed Alkyne-Azide Cycloaddition

Letters in Organic Chemistry (2011)

Marco A. Garcia Zita G. Rios Jaime González Víctor M. Díaz Pérez Nancy Lara

1,2,3-triazoles were synthesized using several alkynes and azides as starting materials in the presence of glucose and catalytic amounts of Fehling reagent. This process is carried out under ambient pressure and temperature with good yields Keywords: Alkynes, azides, Fehling reagent, glucose, 1,2,3-triazoles, copper, pressure, temperature, triazole, sodium

Sodium azide

Alkyne

10.2174/157017811799304232

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Citations (20)

Synthesis of 4-Substituted 2-Phenylaminothiazoles from Amidines. A Convenient Route to 4-Trichloromethylthiazoles

The Journal of Organic Chemistry (2000)

Moisés Romero‐Ortega Adriana Aviles Raymundo Cruz Aydeé Fuentes Rosa María Gómez‐Espinosa

ADVERTISEMENT RETURN TO ISSUEPREVNoteNEXTSynthesis of 4-Substituted 2-Phenylaminothiazoles from Amidines. A Convenient Route to 4-TrichloromethylthiazolesMoisés Romero-Ortega, Adriana Aviles, Raymundo Cruz, Aydee Fuentes, Rosa María Gómez, and Andrés PlataView Author Information Departamento de Química Orgánica, Facultad de Química, Universidad Autónoma del Estado de México, Paseo Colón/Paseo Tollocan s/n Toluca Estado de México, C.P.50000, Mexico, and Instituto de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, Mexico, D.F. [email protected]Cite this: J. Org. Chem. 2000, 65, 21, 7244–7247Publication Date (Web):September 27, 2000Publication History Received22 June 2000Published online27 September 2000Published inissue 1 October 2000https://pubs.acs.org/doi/10.1021/jo0009447https://doi.org/10.1021/jo0009447brief-reportACS PublicationsCopyright © 2000 American Chemical SocietyRequest reuse permissionsArticle Views655Altmetric-Citations16LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Anions,Hydrocarbons,Phenyls,Reaction products,Substituents Get e-Alerts

10.1021/jo0009447

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Citations (19)

Synthesis of Phenylthiomethyl Compounds from Trichloromethyl Derivatives

Synthesis (1999)

Moisés Romero‐Ortega Aydeé Fuentes Carlos González D. Morales Raymundo Cruz

A new method for the conversion of trichloromethyl compounds into the corresponding phenylthiomethyl derivatives by reaction with sodium thiophenolate in the presence of thiophenol is described. This transformation proceeds at room temperature in high yield and has been applied to a variety of trichloromethyl compounds.

Thiophenol

10.1055/s-1999-3376

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Citations (8)

ChemInform Abstract: Alkyne—Azide Cycloaddition Catalyzed by Fe—Cu Nanoparticles.

ChemInform (2012)

Ángel García-Muñoz Jaime González Jessica Trujillo‐Reyes Raúl A. Morales‐Luckie Víctor Sánchez‐Mendieta

Abstract Paramagnetic Fe—Cu nanoparticles are used to catalyze typical azide—alkyne cycloadditions.

Alkyne

10.1002/chin.201235141

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Citations (0)

Diels—Alder Reactions of 2‐Oxazolidinone Dienes in Polar Solvents Using Catalysis or Non‐Conventional Energy Sources.

ChemInform (2005)

Aydeé Fuentes Rafael Martínez‐Palou Hugo A. Jiménez‐Vázquez Francisco Delgado Alicia Reyes

Abstract For Abstract see ChemInform Abstract in Full Text.

Diels–Alder reaction

Diene

10.1002/chin.200522123

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ChemInform Abstract: Synthesis of 4‐Substituted 2‐Phenylaminothiazoles from Amidines. A Convenient Route to 4‐Trichloromethylthiazoles.

ChemInform (2001)

Moisés Romero‐Ortega Adriana Aviles Raymundo Cruz Aydeé Fuentes Rosa María Gómez‐Espinosa

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

10.1002/chin.200110123

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Short and Efficient Synthesis of 3‐Substituted 4‐Oxazolin‐2‐thiones and Their Reactivity.

ChemInform (2007)

Carlos González‐Romero Rafael Martínez‐Palou Hugo A. Jiménez‐Vázquez Aydeé Fuentes Fabiola Jiménez

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Reactivity

10.1002/chin.200730093

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Citations (0)

ChemInform Abstract: The Use of Glucose as Alternative Reducing Agent in Copper‐Catalyzed Alkyne—Azide Cycloaddition.

ChemInform (2012)

Marco A. Garcia Zita G. Rios Jaime González Víctor M. Díaz Pérez Nancy Lara

Abstract An inexpensive method for the synthesis of 1,2,3‐triazoles uses a catalytic system prepared from Fehling reagent and glucose.

Alkyne

Reducing agent

10.1002/chin.201219131

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