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Pd-catalyzed, Cu(I)-mediated cross-couplings of bisarylthiocyclobutenediones with boronic acids and organostannanes.


ABSTRACT: Bisarylthiocyclobutenedione 7 reacted smoothly with a variety of both organostannanes and (hetero)arylboronic acids in the presence of a catalytic amount of Pd and a stoichiometric amount of CuTC to produce symmetrical disubstituted cyclobutenediones in yields that range from 37 to 94% (18 examples).

SUBMITTER: Aguilar-Aguilar A 

PROVIDER: S-EPMC2708074 | biostudies-literature | 2007 Oct

REPOSITORIES: biostudies-literature

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Pd-catalyzed, Cu(I)-mediated cross-couplings of bisarylthiocyclobutenediones with boronic acids and organostannanes.

Aguilar-Aguilar Angélica A   Liebeskind Lanny S LS   Peña-Cabrera Eduardo E  

The Journal of organic chemistry 20070925 22


Bisarylthiocyclobutenedione 7 reacted smoothly with a variety of both organostannanes and (hetero)arylboronic acids in the presence of a catalytic amount of Pd and a stoichiometric amount of CuTC to produce symmetrical disubstituted cyclobutenediones in yields that range from 37 to 94% (18 examples). ...[more]

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