Todas las entradas de: Javier Carreras Pérez Aradros

Baeza et al. European Journal of Organic Chemistry. 2010;2010(29):5607 -5618. Title

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Publicaciones > Baeza et al

Application of Selective Palladium-Mediated Functionalization of the Pyrido%@5B3′,2′:4,5%@5Dpyrrolo%@5B1,2-c%@5Dpyrimidine Heterocyclic System for the Total Synthesis of Variolin B and Deoxyvariolin B

Resumen

Abstract The reaction of protected 3-bromo-2-(bromomethyl)-4-methoxypyrrolo%@5B2,3-b%@5Dpyridine and tosylmethyl isocyanide (TosMIC) afforded a pyrido%@5B3?,2?:4,5%@5Dpyrrolo%@5B1,2-c%@5Dpyrimidine derivative in good yield. This compound was transformed through installation of the pyrimidine moiety in the C5 position, hydrolysis, and decarboxylation in an advanced intermediate for the total or formal synthesis of the naturalalkaloid variolin B. Reaction of 3-bromo-2-(bromomethyl)-4-chloropyrrolo%@5B2,3-b%@5Dpyridine with N-tosylmethyl dichloroformimide as a synthetic TosMIC equivalent afforded trihalo-substituted pyrido%@5B3?,2?:4,5%@5Dpyrrolo%@5B1,2-c%@5Dpyrimidine. This compound was used in a new total synthesis of the alkaloid variolin B by selective and sequential C?N, C?C, and C?O palladium-mediated functionalization at the C9, C5, and C4 positions of the pyrido%@5B3?,2?:4,5%@5Dpyrrolo%@5B1,2-c%@5Dpyrimidine system. A formal synthesis of deoxyvariolin B is also described by using the same synthetic strategy.

Deligeorgiev et al. Phosphorus, Sulfur, and Silicon and the Related Elements. 2010;185(11):2292 -2302. Novel Green Procedure for the Synthesis of 2-Arylbenzothiazoles Under Microwave Irradiation in Peg 200 Or Peg 400

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Publicaciones > Deligeorgiev et al

Novel Green Procedure for the Synthesis of 2-Arylbenzothiazoles Under Microwave Irradiation in Peg 200 Or Peg 400

Resumen

An improved green procedure for the synthesis of 2-aryl- and 2-hetarylbenzothiazoles by condensation of equivalent amounts of 2,2?-diaminodiphenyldisulfides or 2-aminothiophenols and various aromatic aldehydes in PEG 200/400 under microwave irradiation has been developed. This method allows the synthesis of 2-arylbenzothiazoles in high yields and with high purity regardless of the state of the starting compounds (liquid or solid) or the nature of the substituents in the aromatic ring.

Deligeorgiev et al. Coloration Technology. 2010;126(2):55 -80. Styryl dyes – synthesis and applications during the last 15 years

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Publicaciones > Deligeorgiev et al

Styryl dyes – synthesis and applications during the last 15 years

Resumen

One of the most widely used and important groups of functional dyes are the styryl dyes and a review of this functional dye class has not been published for more than 15?years. In this review article, we describe the new trends in the synthesis of a range of novel intermediates and styryl dyes and include the most interesting examples of their high-tech applications. However, this review is not intended to be comprehensive because of the large number of styryl dye studies that have been carried out in this time. Styryl cyanine dyes are widely used in optical recording media in laser discs, as flexible dyes, laser dyes, as optical sensitisers and in various other fields, for example dye-sensitised solar cells and dyes with non-linear optical properties. Additionally, the most important applications for these dyes are in bio-labelling and in medicinal analysis.

Deligeorgiev et al. Mini-Reviews in Organic Chemistry. 2010;7(1):44 -53. Green chemistry in organic synthesis.

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Publicaciones > Deligeorgiev et al

Green chemistry in organic synthesis.

1. University of Sofia, Faculty of Chemistry, 1164 Sofia, Bulgaria.  2. University of Alcalá, Faculty of Pharmacy, 28871 Alcalá de Henares, Madrid, Spain.

Resumen

The development of the concepts for "Green Chemistry" and the main principles of this field are reviewed. Examples of the application of these principles in different areas of chemistry are included. The frequently used alternative solvents (green solvents - water, PEG, perfluorinated solvents, supercritical liquids) in preparative organic chemistry are described. The present and the future developments of green chemistry in education and organic chemical technology are considered. © 2010 Bentham Science Publishers Ltd.

Deligeorgiev et al. Coloration Technology. 2010;126(1):24 -30. Novel environmentally benign procedure for the synthesis of 2-aryl- and 2-hetaryl-4(3H)-quinazolinones

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Publicaciones > Deligeorgiev et al

Novel environmentally benign procedure for the synthesis of 2-aryl- and 2-hetaryl-4(3H)-quinazolinones

Resumen

A novel environmentally benign procedure for the synthesis of 2-aryl- or 2-hetaryl-4(3H)-quinazolinones by condensation of anthranilamide with various aromatic aldehydes in polyethylene glycol under microwave irradiation has been developed. In contrast with other reported methods, this procedure provides the corresponding quinazolinones with good to high yields and purity, in very short reaction times and without the use of an oxidant.

Deligeorgiev et al. Ultrasonics Sonochemistry 2010;17(5):783 -788. An easy and fast ultrasonic selective S-alkylation of hetaryl thiols at room temperature

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Publicaciones > Deligeorgiev et al

An easy and fast ultrasonic selective S-alkylation of hetaryl thiols at room temperature

Resumen

A series of 2-alkylthio derivatives of hetaryl thiols were synthesized by selective S-alkylation with alkyl halides (bromides and iodides) with ultrasonic irradiation at room temperature. The reaction was found to be generally applicable to hetaryl thiol derivatives with different substituents in the aromatic nucleus and various alkyl halides. The reaction gives high to excellent yields of products with high purity.

Virumbrales et al. Org Biomol Chem. 2018;16(15):2623-2628. Gold(i)-catalyzed diastereoselective synthesis of 1-α-oxybenzyl-1H-indenes.

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Publicaciones > Virumbrales et al

Gold(i)-catalyzed diastereoselective synthesis of 1-α-oxybenzyl-1H-indenes.

Área de Química Orgánica, Departamento de Química, Facultad de Ciencias, Universidad de Burgos, Pza. Misael Bañuelos s/n, 09001 Burgos, Spain.

arsd@ubu.es

Abstract

The gold(i)-catalyzed oxycyclization of β-aryl monosubstituted o-(alkynyl)styrenes gives rise to 1-α-methoxy or 1-α-hydroxybenzyl-1H-indenes in a diastereospecific way. In contrast to β,β-disubstituted o-(alkynyl)styrenes, the stereochemical outcome of this process, diastereospecific reaction supports the higher contribution of a gold intermediate with a cyclopropylcarbene-like character.

García-García et al. J Org Chem. 2017;82(2):1155-1165. Synthesis of Functionalized 1H-Indenes and Benzofulvenes through Iodocyclization of o-(Alkynyl)styrenes.

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Publicaciones > García-García et al

Synthesis of Functionalized 1H-Indenes and Benzofulvenes through Iodocyclization of o-(Alkynyl)styrenes.

1. Departamento de Química Orgánica y Química Inorgánica, Universidad de Alcalá , 28871 Alcalá de Henares, Madrid, Spain.  2. Área de Química Orgánica, Departamento de Química, Facultad de Ciencias, Universidad de Burgos , Pza. Misael Bañuelos s/n, 09001 Burgos, Spain.  3. Instituto Universitario de Química Organometálica "Enrique Moles", Universidad de Oviedo , C/Julián Clavería, 8, 33006 Oviedo, Spain.

Abstract

A convenient method for the preparation of synthetically useful 3-iodoindene derivatives has been developed. This protocol, based on the 5-endo iodocyclization reaction of o-(alkynyl)styrenes, represents one of the scarce examples of halocyclizations using olefins as nucleophilic counterparts and allows the synthesis of both 3-iodo-1H-indenes (from β-alkyl-β-alkyl/aryl-o-(alkynyl)styrenes) and 3-iodobenzofulvenes (from β,β-diaryl-o-(alkynyl)styrenes) in good yields under mild reaction conditions. In addition, related alkoxyiodocyclization processes are described, which are particularly interesting in their intramolecular version because they allow the synthesis of heteropolycyclic structures containing the indene core. Finally, the usefulness of the prepared 3-iodoindenes has been demonstrated by the synthesis of several polysubstituted indene derivatives through conventional palladium-catalyzed cross-coupling reactions and iodine-lithium exchange processes.

Fernández-García et al. Advanced Synthesis %@26 Catalysis. 2017;359(17):3035 -3051. Title

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Publicaciones > Fernández-García et al

Gold-Catalyzed Cycloisomerizations of Functionalyzed Cyclopropyl Alkynes: the Cases of Carboxamides and Alcohols

Resumen

Push-pull alkynylcyclopropane derivatives are claimed as suitable and active substrates for gold-catalyzed transformations. Thus, 2(3H)-azepinones can be readily prepared from alkynylcyclopropanecarboxamides through a nucleophilic addition/cyclopropane ring-opening cascade process and, in this manuscript, the scope and the limitations of such reaction sequence are reported. The cascade reaction is general and occurs with complete regio- and quimioselection to form the seven-membered heterocycles with the exception of primary alkyl-substituted alkynylcyclopropanecarboxamides that render 4-methoxy-6-oxo-4-enenitriles in moderate yields. Additionally, less activated alkynylcyclopropylmethanols undergo regioselective cycloisomerization at low temperature leading to oxabicyclo%@5B4.1.0%@5Dheptanes. Notably, the cyclopropane ring opening of these adducts takes place under thermal conditions to form dihydropyranones.

Aguilar et al. Chem Rev. 2016;116(14):8256-311. 1,3-Dien-5-ynes: Versatile Building Blocks for the Synthesis of Carbo- and Heterocycles.

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Publicaciones > Aguilar et al

1,3-Dien-5-ynes: Versatile Building Blocks for the Synthesis of Carbo- and Heterocycles.

1. Instituto Universitario de Química Organometálica "Enrique Moles", Departamento de Química Orgánica e Inorgánica, Universidad de Oviedo , C/Julián Clavería 8, 33006 Oviedo, Spain.  2. Departamento de Química, Área de Química Orgánica, Facultad de Ciencias, Universidad de Burgos , Pza. Misael Bañuelos s/n, 09001 Burgos, Spain.  3. Departamento de Química Orgánica y Química Inorgánica, Universidad de Alcalá , 28871 Alcalá de Henares, Madrid, Spain.

Abstract

1,3-Dien-5-ynes have been extensively used as starting materials for the synthesis of a wide number of different carbo- and heterocycles. The aim of this review is to give an overview of their utility in organic synthesis, highlighting the variety of compounds that can be directly accessed from single reactions over these systems. Thus, cycloaromatization processes are initially commented, followed by reactions directed toward the syntheses of five-membered rings, other carbocycles and, finally, heterocycles. The diverse methodologies that have been developed for the synthesis of each of these types of compounds from 1,3-dien-5-ynes are presented, emphasizing the influence of the reaction conditions and the use of additional reagents in the outcome of the transformations.