Organocatalysis, the catalysis with low-molecular weight catalysts where a metal is not part of the catalytic principle, can be as efficient and selective as metal- or biocatalysis. Important discoveries in this area include novel Lewis base-catalyzed enantioselective processes and, more recently, simple Brønsted acid organocatalysts that rival the efficiency of traditional metal-based asymmetric Lewis acid-cata-lysts. Contributions to organocatalysis from our laboratories include several new and broadly useful concepts such as enamine catalysis and asymmetric counteranion directed catalysis. Our lab has discov-ered the proline-catalyzed direct asymmetric intermolecular aldol reac-tion and introduced several other organocatalytic reactions
Abstract: Synthetic efficiency requires reactions that are both selective and economical in terms of...
Asymmetric organocatalysis is now recognized as the third pillar of asymmetric synthesis. Recent yea...
The use of simple (S)-proline as catalyst for the intermolecular direct aldol reaction at the beginn...
Organocatalysis, catalysis with low-molecular weight catalysts in which a metal is not part of the c...
For a long time, there seemed to have been an unwritten rule that organocatalysts, in contrast to tr...
The field of asymmetric organocatalysis is rapidly developing and attracts an increasing number of r...
In the year 2000, Accounts of Chemical Research published a landmark special edition on the timely s...
Catalysis fulfills the promise that high-yielding chemical transformations will require little energ...
Catalysis fulfills the promise that high-yielding chemical transformations will require little energ...
During the last 20 years, organocatalysis has significantly advanced as a field. Thanks to contribut...
Chemical synthesis is one of the key technologies underlying modern drug discovery and development. ...
In recent years there has been an accelerated rate of development in the field of organocatalysis, w...
Organocatalysis, that is the use of small organic molecules to catalyse organic transformations, has...
In the last decade a remarkable expansion of a new field has been accomplished, the asymmetric organ...
Reactions carried out with substoichiometric quantities of organic molecules as catalysts has receiv...
Abstract: Synthetic efficiency requires reactions that are both selective and economical in terms of...
Asymmetric organocatalysis is now recognized as the third pillar of asymmetric synthesis. Recent yea...
The use of simple (S)-proline as catalyst for the intermolecular direct aldol reaction at the beginn...
Organocatalysis, catalysis with low-molecular weight catalysts in which a metal is not part of the c...
For a long time, there seemed to have been an unwritten rule that organocatalysts, in contrast to tr...
The field of asymmetric organocatalysis is rapidly developing and attracts an increasing number of r...
In the year 2000, Accounts of Chemical Research published a landmark special edition on the timely s...
Catalysis fulfills the promise that high-yielding chemical transformations will require little energ...
Catalysis fulfills the promise that high-yielding chemical transformations will require little energ...
During the last 20 years, organocatalysis has significantly advanced as a field. Thanks to contribut...
Chemical synthesis is one of the key technologies underlying modern drug discovery and development. ...
In recent years there has been an accelerated rate of development in the field of organocatalysis, w...
Organocatalysis, that is the use of small organic molecules to catalyse organic transformations, has...
In the last decade a remarkable expansion of a new field has been accomplished, the asymmetric organ...
Reactions carried out with substoichiometric quantities of organic molecules as catalysts has receiv...
Abstract: Synthetic efficiency requires reactions that are both selective and economical in terms of...
Asymmetric organocatalysis is now recognized as the third pillar of asymmetric synthesis. Recent yea...
The use of simple (S)-proline as catalyst for the intermolecular direct aldol reaction at the beginn...