A convenient, instrumentally simple, and efficient methodology to transform 1,2-dihydropyridines into benzoic esters is described. The generated multisubstituted benzoic esters feature different topologies spanning from simple aromatic rings to fused benzocycloalkane systems. As an extension of this methodology, these benzoic esters are efficiently transformed into an array of fluorenone frameworks featuring interesting and novel topological patterns.This research was supported by the Spanish Ministerio de Economía y Competitividad (MINECO) and the European Regional Development Fund (CTQ2011-28417-C02-02 and CTQ2015-63894-P). M.C.P.-R. thanks the Spanish Ministerio de Educación y Ciencia (MEC) for an FPI Grant. M.I. thanks the Agencia Nacio...
International audienceA convenient and versatile procedure for the straightforward synthesis of subs...
Fluorine-containing organic scaffolds are of significant interest in medicinal chemistry. The incorp...
Palladium-catalyzed dual C–H functionalization of benzophenones to form fluorenones by oxidative deh...
A convenient, instrumentally simple, and efficient methodology to transform 1,2-dihydropyridines int...
Trabajo presentado en la XXVI Reunión Bienal de Química Orgánica de la Real Sociedad Española de Quí...
International audienceExtended fluorenones represent a particular class of polycyclic compounds. The...
This report illustrates BF3·OEt2 promoted intramolecular cascade cycloaromatization of 1,7-ynones to...
An efficient methodology for the synthesis of benzofuropyridines and dibenzofurans from fluoropyridi...
An efficient methodology for the synthesis of benzofuropyridines and dibenzofurans from fluoropyridi...
A synthetic sequence to the benzo[j]fluoranthene nucleus is described. Crucial steps of the procedur...
A new method has been developed for the synthesis of tetrahydro-2H-fluorenes based on a Pd(0)-cataly...
A synthetic sequence to the benzo[<i>j</i>]fluoranthene nucleus is described. Crucial steps of the...
Natural products bearing benzo[j]fluoranthene skeleton can be found in the metabolites of various fu...
3,6,8,11-Tetramethoxybenzo[j]fluoranthene can be made from 1,6-dimethoxynaphthalene in a one-pot fer...
An unprecedented KHMDS-promoted domino reaction to furnish hydroxyfluoranthenes is described. Biaryl...
International audienceA convenient and versatile procedure for the straightforward synthesis of subs...
Fluorine-containing organic scaffolds are of significant interest in medicinal chemistry. The incorp...
Palladium-catalyzed dual C–H functionalization of benzophenones to form fluorenones by oxidative deh...
A convenient, instrumentally simple, and efficient methodology to transform 1,2-dihydropyridines int...
Trabajo presentado en la XXVI Reunión Bienal de Química Orgánica de la Real Sociedad Española de Quí...
International audienceExtended fluorenones represent a particular class of polycyclic compounds. The...
This report illustrates BF3·OEt2 promoted intramolecular cascade cycloaromatization of 1,7-ynones to...
An efficient methodology for the synthesis of benzofuropyridines and dibenzofurans from fluoropyridi...
An efficient methodology for the synthesis of benzofuropyridines and dibenzofurans from fluoropyridi...
A synthetic sequence to the benzo[j]fluoranthene nucleus is described. Crucial steps of the procedur...
A new method has been developed for the synthesis of tetrahydro-2H-fluorenes based on a Pd(0)-cataly...
A synthetic sequence to the benzo[<i>j</i>]fluoranthene nucleus is described. Crucial steps of the...
Natural products bearing benzo[j]fluoranthene skeleton can be found in the metabolites of various fu...
3,6,8,11-Tetramethoxybenzo[j]fluoranthene can be made from 1,6-dimethoxynaphthalene in a one-pot fer...
An unprecedented KHMDS-promoted domino reaction to furnish hydroxyfluoranthenes is described. Biaryl...
International audienceA convenient and versatile procedure for the straightforward synthesis of subs...
Fluorine-containing organic scaffolds are of significant interest in medicinal chemistry. The incorp...
Palladium-catalyzed dual C–H functionalization of benzophenones to form fluorenones by oxidative deh...