A palladium-catalyzed regio- and stereoselective intermolecular tandem reaction of alkynes and unactivated 1,6-enols in ionic liquids is described, providing a practical, efficient, and versatile method for the synthesis of functionalized 1,6-dienes in moderate to good yields. The present reaction has high functional-group tolerance and gives products on a gram scale. Mechanistic studies indicate that the reaction might proceed via a chain-walking mechanism
A palladium-catalyzed aryldifluoroalkylation of alkynes with ethyl difluoroiodoacetate and arylboron...
A catalytic method to prepare highly substituted 1,3-dienes from two different alkenes is described ...
A novel approach to substrate design led to the development of charge de-localized extended Michael...
A new, efficient ionic liquid based synthetic procedure was developed for the preparation of highly ...
A Palladium/imidazolium chloride system has been used to mediate the dimerization of terminal alkyne...
In organic chemistry ionic liquids (ILs) have emerged as safe and recyclable reaction solvents. In t...
An unprecedented palladium-catalyzed allylic alkylation of pronucleophiles with unactivated skipped ...
Terminal alkynes undergo oxidative-coupling smoothly in the presence of the CuCl-TMEDA catalytic sys...
A series of <i>O</i>- and <i>N</i>-linked 1,6-enynes (e.g., <b>11</b>) have been prepared with each ...
The Lautens group has investigated the use of metal catalysts for the domino synthesis of heterocycl...
Aryl and alkenylpalladium compounds generated by oxidative addition of a palladium(0) catalyst to th...
Imidazolium-based ionic liquids (ILs) serve both as recyclable reaction media and as precatalysts fo...
A palladium-catalyzed difunctionalization of bicyclic alkenes with organoammonium salts and organobo...
<p>An effective and simple protocol for the Diels–Alder reactions catalyzed and mediated by ionic li...
Ce travail décrit une méthodologie de synthèse pallado-catalysée en milieu liquide ionique [BMIM][BF...
A palladium-catalyzed aryldifluoroalkylation of alkynes with ethyl difluoroiodoacetate and arylboron...
A catalytic method to prepare highly substituted 1,3-dienes from two different alkenes is described ...
A novel approach to substrate design led to the development of charge de-localized extended Michael...
A new, efficient ionic liquid based synthetic procedure was developed for the preparation of highly ...
A Palladium/imidazolium chloride system has been used to mediate the dimerization of terminal alkyne...
In organic chemistry ionic liquids (ILs) have emerged as safe and recyclable reaction solvents. In t...
An unprecedented palladium-catalyzed allylic alkylation of pronucleophiles with unactivated skipped ...
Terminal alkynes undergo oxidative-coupling smoothly in the presence of the CuCl-TMEDA catalytic sys...
A series of <i>O</i>- and <i>N</i>-linked 1,6-enynes (e.g., <b>11</b>) have been prepared with each ...
The Lautens group has investigated the use of metal catalysts for the domino synthesis of heterocycl...
Aryl and alkenylpalladium compounds generated by oxidative addition of a palladium(0) catalyst to th...
Imidazolium-based ionic liquids (ILs) serve both as recyclable reaction media and as precatalysts fo...
A palladium-catalyzed difunctionalization of bicyclic alkenes with organoammonium salts and organobo...
<p>An effective and simple protocol for the Diels–Alder reactions catalyzed and mediated by ionic li...
Ce travail décrit une méthodologie de synthèse pallado-catalysée en milieu liquide ionique [BMIM][BF...
A palladium-catalyzed aryldifluoroalkylation of alkynes with ethyl difluoroiodoacetate and arylboron...
A catalytic method to prepare highly substituted 1,3-dienes from two different alkenes is described ...
A novel approach to substrate design led to the development of charge de-localized extended Michael...