A novel and efficient method for the synthesis of highly substituted benzobicyclo[2.2.2]octane skeletons has been explored. Under UV-light irradiation, o-divinylbenzenes underwent a pericyclic reaction to form the cyclic o-quinodimethane intermediates which were subsequently reacted with olefins through [4+2] addition to construct the benzobicyclo[2.2.2]octane skeletons in mild conditions. Gram scale reactions demonstrated the synthetic potential application of this protocol
Chapter 1. A brief overview of the preparation and uses of o-quinodimethanes and benzocyclobutenes i...
An enantioselective Michael addition– four-atom ring expansion cascade reaction involving cyclobutan...
A highly regio- and diastereoselective visible-light-promoted [2 + 2] cycloaddition between readily ...
The photolysis of substituted <i>o</i>-divinylbenzenes promotes a one-step and metal-free conversion...
A novel Lewis acid catalyzed formal intramolecular [3 + 3] cross-cycloaddition (IMCC) of cyclopropan...
A novel Lewis acid catalyzed formal intramolecular [3 + 3] cross-cycloaddition (IMCC) of cyclopropan...
A novel Lewis acid catalyzed formal intramolecular [3 + 3] cross-cycloaddition (IMCC) of cyclopropan...
A novel Lewis acid catalyzed formal intramolecular [3 + 3] cross-cycloaddition (IMCC) of cyclopropan...
International audienceAn enantioselective Michael addition-four-atom ring expansion cascade reaction...
International audienceAn enantioselective Michael addition-four-atom ring expansion cascade reaction...
International audienceAn enantioselective Michael addition-four-atom ring expansion cascade reaction...
An enantioselective Michael addition– four-atom ring expansion cascade reaction involving cyclobutan...
An enantioselective Michael addition– four-atom ring expansion cascade reaction involving cyclobutan...
An enantioselective Michael addition– four-atom ring expansion cascade reaction involving cyclobutan...
International audienceAn enantioselective Michael addition-four-atom ring expansion cascade reaction...
Chapter 1. A brief overview of the preparation and uses of o-quinodimethanes and benzocyclobutenes i...
An enantioselective Michael addition– four-atom ring expansion cascade reaction involving cyclobutan...
A highly regio- and diastereoselective visible-light-promoted [2 + 2] cycloaddition between readily ...
The photolysis of substituted <i>o</i>-divinylbenzenes promotes a one-step and metal-free conversion...
A novel Lewis acid catalyzed formal intramolecular [3 + 3] cross-cycloaddition (IMCC) of cyclopropan...
A novel Lewis acid catalyzed formal intramolecular [3 + 3] cross-cycloaddition (IMCC) of cyclopropan...
A novel Lewis acid catalyzed formal intramolecular [3 + 3] cross-cycloaddition (IMCC) of cyclopropan...
A novel Lewis acid catalyzed formal intramolecular [3 + 3] cross-cycloaddition (IMCC) of cyclopropan...
International audienceAn enantioselective Michael addition-four-atom ring expansion cascade reaction...
International audienceAn enantioselective Michael addition-four-atom ring expansion cascade reaction...
International audienceAn enantioselective Michael addition-four-atom ring expansion cascade reaction...
An enantioselective Michael addition– four-atom ring expansion cascade reaction involving cyclobutan...
An enantioselective Michael addition– four-atom ring expansion cascade reaction involving cyclobutan...
An enantioselective Michael addition– four-atom ring expansion cascade reaction involving cyclobutan...
International audienceAn enantioselective Michael addition-four-atom ring expansion cascade reaction...
Chapter 1. A brief overview of the preparation and uses of o-quinodimethanes and benzocyclobutenes i...
An enantioselective Michael addition– four-atom ring expansion cascade reaction involving cyclobutan...
A highly regio- and diastereoselective visible-light-promoted [2 + 2] cycloaddition between readily ...