International audienceA series of 4′-alkyl-2′-hydroxyacetophenones were prepared by Suzuki cross-coupling reactions of 4′-bromo-2′-hydroxyacetophenone. In these reactions, alkyl(trifluoro)borates were found to be better reactants than alkylboronic acids. 4′-Alkyl-2′-hydroxyacetophenones are key intermediates for the further synthesis of -lipoflavonoids that are more readily incorporated into lipid bilayer membranes than flavonoids and should, therefore, have superior -biological effects through increased bioavailability
This paper reports some studies aiming at the developement of a general protocol useful for the synt...
The first method for achieving alkyl–alkyl Suzuki reactions of unactivated secondary alkyl chlorides...
A recently developed method for the nearambient generation of difluorovinylzinc reagents has facilit...
Herein, we report the use of the Suzuki–Miyaura cross-coupling reaction for the preparation of a lib...
Isoflavones were synthesized via Suzuki–Miyaura coupling of 3-iodochromones and para-methoxybenzene-...
A series of alkenyl phenylboronic acid pinacol esters have been synthesized via an olefin cross-meta...
This thesis includes regioselective palladium(0)-catalyzed Suzuki cross-coupling reactions of quinol...
Organotrifluoroborates have emerged in the past decade as suitable nucleophilic partners for the Suz...
A series of alkenyl phenylboronic acid pinacol esters has been synthesized via an olefin cross-metat...
An efficient and versatile synthesis of 3-alkenylbutenolides through direct Suzuki–Miyaura cross cou...
Efficient Csp3-Csp3 Suzuki couplings have been developed with both potassium cyclopropyl- and alkoxy...
A new class of flavone which possess an aryl radical substituted in the A ring via C-C bond, arylchr...
While the Suzuki coupling has gained paramount importance, the basic set-up of the reaction has rema...
A variety of 4'- and 3-C-aryl-quercetin derivatives were conveniently synthesized via Suzuki-Myaura ...
International audienceStarting from 5,5′-dihalo-1′-pentyl-2H-spiro[furo[2,3-b]pyridine-3,3′-indolin]...
This paper reports some studies aiming at the developement of a general protocol useful for the synt...
The first method for achieving alkyl–alkyl Suzuki reactions of unactivated secondary alkyl chlorides...
A recently developed method for the nearambient generation of difluorovinylzinc reagents has facilit...
Herein, we report the use of the Suzuki–Miyaura cross-coupling reaction for the preparation of a lib...
Isoflavones were synthesized via Suzuki–Miyaura coupling of 3-iodochromones and para-methoxybenzene-...
A series of alkenyl phenylboronic acid pinacol esters have been synthesized via an olefin cross-meta...
This thesis includes regioselective palladium(0)-catalyzed Suzuki cross-coupling reactions of quinol...
Organotrifluoroborates have emerged in the past decade as suitable nucleophilic partners for the Suz...
A series of alkenyl phenylboronic acid pinacol esters has been synthesized via an olefin cross-metat...
An efficient and versatile synthesis of 3-alkenylbutenolides through direct Suzuki–Miyaura cross cou...
Efficient Csp3-Csp3 Suzuki couplings have been developed with both potassium cyclopropyl- and alkoxy...
A new class of flavone which possess an aryl radical substituted in the A ring via C-C bond, arylchr...
While the Suzuki coupling has gained paramount importance, the basic set-up of the reaction has rema...
A variety of 4'- and 3-C-aryl-quercetin derivatives were conveniently synthesized via Suzuki-Myaura ...
International audienceStarting from 5,5′-dihalo-1′-pentyl-2H-spiro[furo[2,3-b]pyridine-3,3′-indolin]...
This paper reports some studies aiming at the developement of a general protocol useful for the synt...
The first method for achieving alkyl–alkyl Suzuki reactions of unactivated secondary alkyl chlorides...
A recently developed method for the nearambient generation of difluorovinylzinc reagents has facilit...