J
J. Carlos Menéndez
Researcher at Complutense University of Madrid
Publications - 336
Citations - 7983
J. Carlos Menéndez is an academic researcher from Complutense University of Madrid. The author has contributed to research in topics: Catalysis & Michael reaction. The author has an hindex of 37, co-authored 317 publications receiving 6784 citations. Previous affiliations of J. Carlos Menéndez include Université Paul Cézanne Aix-Marseille III & Universiti Sains Malaysia.
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Comprar Medicinal Chemistry of Anticancer Drugs | Carmen Avendano | 9780444528247 | Elsevier Science
TL;DR: Menendez et al. as discussed by the authors present a tienda online donde Comprar Medicinal Chemistry of Anticancer Drugs al precio 160,09 € de Carmen Avendano | J. Carlos Menendez.
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Amide N-arylation with p-tolyllead triacetate
TL;DR: The Narylation of several types of amidic nitrogen atoms, including those found in carboxamides, sulfonamides and carboxylic acid imides, was carried out by treatment of their sodium salts with p-tolyllead triacetate in the presence of copper (II) acetate.
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Comparative study of synthetic approaches to 1-arylmethylenepyrazino[2,1-b]quinazoline-3,6-diones
TL;DR: In this paper, the transformation of 3-arylmethylenepiperazine-2,5-diones (1) into 1-ylmethylene-2.4-dihydro-1H-pyrazino[2,1-b]quinazoline-3,6-dionses (2) was studied.
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A facile three-component [3+2]-cycloaddition/annulation domino protocol for the regio- and diastereoselective synthesis of novel penta- and hexacyclic cage systems, involving the generation of two heterocyclic rings and five contiguous stereocenters
Raju Suresh Kumar,Hasnah Osman,Subbu Perumal,J. Carlos Menéndez,Mohamed Ashraf Ali,Rusli Ismail,Tan Soo Choon +6 more
TL;DR: In this paper, an expedient, three-component, [3+2]-cycloaddition/annulation domino protocol for the synthesis of a series of cage penta- and hexacyclic compounds in good to excellent yields is described.
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Axial chirality of 4-arylpyrazolo[3,4-b]pyridines. Conformational analysis and absolute configuration.
Pethaiah Gunasekaran,Subbu Perumal,J. Carlos Menéndez,Michele Mancinelli,Silvia Ranieri,Andrea Mazzanti +5 more
TL;DR: The stereodynamic behavior of a series of pyrazolo[3,4-b]pyridines was studied and conformational enantiomers or conformational diastereoisomers depending on the local symmetry of the aryl substituent were generated, with very high rotational barriers despite the absence of ortho-substituents.