The synthesis of an achiral skipped bis(1,3-diene) substrate was achieved, which was shown to undergo an enantioselective, diastereotopic group-selective, intramolecular Diels-Alder reaction
Theoretical studies were performed on BH3,BF3 and BLA acting as catalysts in the [4+2] cycloaddition...
Abstract: Desymmetrisation processes allow a rapid and stereocontrolled elaboration of readily avail...
A ring closing metathesis reaction of dienes and a ring closing enyne metathesis reaction derived fr...
The synthesis of an achiral skipped bis(1,3-diene) substrate was achieved, which was shown to underg...
We report the combination of an intramolecular Diels-Alder (IMDA) reaction and a desymmetrisation pr...
[Introduction] The Diels-Aider reaction is one of the most powerful and widely exploited methods av...
The development and synthesis of a novel class of C2-symmetric outer ring dienes is described. Six ...
A highly efficient method for the enantioselective synthesis of 1,4-dienes (skipped dienes) with a m...
Readily available and stable substituted [3]- dendralenes undergo highly chemo-, regio-, diastereo-...
The enantioselective total synthesis of (-)-dactylolide is reported. The absolute stereochemistry of...
The desymmetrization of symmetric compounds is a useful approach to obtain chiral building blocks. R...
The enantioselective total synthesis of (-)-dactylolide is reported. The absolute stereochemistry of...
The atroposelective desymmetrization of N-arylmaleimides was realized by means of a primary amine ca...
Although the Diels-Alder (DA) reaction of 2-cyclohexenones and 1,3-dienes is in principle an elegant...
A novel approach for exo/endo stereocontrol of intramolecular Diels-Alder reactions is described. Su...
Theoretical studies were performed on BH3,BF3 and BLA acting as catalysts in the [4+2] cycloaddition...
Abstract: Desymmetrisation processes allow a rapid and stereocontrolled elaboration of readily avail...
A ring closing metathesis reaction of dienes and a ring closing enyne metathesis reaction derived fr...
The synthesis of an achiral skipped bis(1,3-diene) substrate was achieved, which was shown to underg...
We report the combination of an intramolecular Diels-Alder (IMDA) reaction and a desymmetrisation pr...
[Introduction] The Diels-Aider reaction is one of the most powerful and widely exploited methods av...
The development and synthesis of a novel class of C2-symmetric outer ring dienes is described. Six ...
A highly efficient method for the enantioselective synthesis of 1,4-dienes (skipped dienes) with a m...
Readily available and stable substituted [3]- dendralenes undergo highly chemo-, regio-, diastereo-...
The enantioselective total synthesis of (-)-dactylolide is reported. The absolute stereochemistry of...
The desymmetrization of symmetric compounds is a useful approach to obtain chiral building blocks. R...
The enantioselective total synthesis of (-)-dactylolide is reported. The absolute stereochemistry of...
The atroposelective desymmetrization of N-arylmaleimides was realized by means of a primary amine ca...
Although the Diels-Alder (DA) reaction of 2-cyclohexenones and 1,3-dienes is in principle an elegant...
A novel approach for exo/endo stereocontrol of intramolecular Diels-Alder reactions is described. Su...
Theoretical studies were performed on BH3,BF3 and BLA acting as catalysts in the [4+2] cycloaddition...
Abstract: Desymmetrisation processes allow a rapid and stereocontrolled elaboration of readily avail...
A ring closing metathesis reaction of dienes and a ring closing enyne metathesis reaction derived fr...
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