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J. L. Marco

Researcher at Spanish National Research Council

Publications -  76
Citations -  950

J. L. Marco is an academic researcher from Spanish National Research Council. The author has contributed to research in topics: Proton & Michael reaction. The author has an hindex of 15, co-authored 76 publications receiving 871 citations. Previous affiliations of J. L. Marco include Complutense University of Madrid.

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Friedländer reaction on 2-amino-3-cyano-4H-pyrans : Synthesis of derivatives of 4H-pyran [2,3-b] quinoline, new tacrine analogues

TL;DR: The Friedlander reaction of densely functionalized 2-amino-3-cyano-4H-pyrans (1) with cyclohexanone has afforded in one step and good yield 5.

Measurements of differential jet cross sections in proton-proton collisions at √s=7 TeV with the CMS detector

S. Chatrchyan, +2167 more
TL;DR: In this paper, the LHC protonproton collisions at ffiffi s p 1⁄4 7 TeV, corresponding to 5:0 fb 1 of integrated luminosity, have been collected with the CMS detector and measured cross sections are corrected for detector effects and compared to perturbative QCD predictions at next-to-leading order, using five sets of parton distribution functions.
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The first asymmetric synthesis of polyfunctionalized 4H-pyrans via Michael addition of malononitrile to 2-acyl acrylates

TL;DR: In this article, the first asymmetric synthesis of 4H-pyrans (4 ) has been developed; a detailed X-ray structural and stereochemical study has established as R the absolute configuration at the new stereocenter in compounds 4.
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Measurement of the top quark mass in the all- jets final state at root s=13 TeV and combination with the lepton plus jets channel

Albert M. Sirunyan, +2251 more
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Studies into the synthesis of derivatives of 4-amino-2,3-dihydroisothiazole 1,1-dioxides and 4-amino-1,2-oxathiole 2,2-dioxides: The search for linked π-system containing analogues as potential inhibitors of HIV-1 reverse transcriptase

TL;DR: In this paper, the synthesis and anti HIV-1 activity of new derivatives of 4-amino-1,2-oxathiole 2,2dioxide (3, 5, 6 and 9) and 4amino 2,3-dihydroisothiazole 1,l-dioxide, a new heterocyclic ring system, is described.